Metrics
Publication
453
Open Access
17
UN Sustainable Development Goals
Announcements & Documents
Lesson Materiels
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Education
2004 - 2009
2004 - 2009Post Doctorate of Medicine
Marmara University, School of Medicine, Internal Medical Sciences, Turkey
1999 - 2004
1999 - 2004Expertise In Medicine
Marmara University, School of Medicine, Internal Medical Sciences, Turkey
1992 - 1999
1992 - 1999Undergraduate
Istanbul University, Cerrahpaşa Tıp Fakültesi, Cerrahpaşa Tıp Pr. (İngilizce), Turkey
Research Areas
Health Sciences
Research Areas Based on Academic Activities
Avesis Research Areas
WoS Research Areas
Scopus Research Areas
Managerial Experience
2020 - Continues
2020 - ContinuesSurplus Coordinator
Marmara University, School of Medicine, Internal Medical Sciences
2020 - Continues
2020 - ContinuesPostgraduate Education Commission Member
Marmara University, School of Medicine, Internal Medical Sciences
Non Academic Experience
2013 - 2015
2013 - 2015Academic Postdoc research fellow
University of Birmingham Center for Endocrinology Diabetes and Metabolism, Academic Postdoc research fellow
2008 - 2008
2008 - 2008Postdoc Research fellow
University of Cambridge Institute of Metabolic Sciences, Postdoc Research fellow
Designed Courses and Trainings
November 2022
November 2022Çocuk Endokrinolojisi Ve Onkolojisi Kesişim Noktaları Ortak Sempozyumu
Academic Units - Training
Güran T.
October 2022
October 202226.Ulusal Pediatrik Endokrinoloji ve Diyabet Kongresi'
Academic Units - Training
Güran T.
December 2019
December 2019Pediatrik Endokrinoloji İleri Kursu (PEİK)
Academic Units - Training
Güran T.
Representation and Promotion Activities
Saglik Bakanligi Ulusal Konjenital Adrenal Hiperplazi Taramasi Bilim Danisma Kurulu uyesi
Institutional Representation, Saglik Bakanligi, Turkey, Ankara, 2017 - 2022
Articles
All (72)
SCI-E, SSCI, AHCI (66)
SCI-E, SSCI, AHCI, ESCI (70)
ESCI (4)
Scopus (68)
TRDizin (6)
Other Publications (1)
2026
20261. Contemporary global management of 21-hydroxylase deficiency congenital adrenal hyperplasia in early infancy: a multi-national registry study
Lim D. B., Bryce J., Ali S. R., Tseretopoulou X., Birkebaek N. H., Hannema S. E., et al.
European Journal of Endocrinology
, vol.194, no.2, pp.123-135, 2026 (SCI-Expanded, Scopus)
2026
20262. Positive neonatal screening test for congenital adrenal hyperplasia in a case with 3β-hydroxysteroid dehydrogenase type 2 deficiency
Anik M., Erdogan D., Baris T., Arslanoglu I., Canbaz A. T., GÜRAN T.
Journal of Pediatric Endocrinology and Metabolism
, vol.39, no.2, pp.193-198, 2026 (SCI-Expanded, Scopus)
2025
20253. Phenotypic Variation and Pubertal Outcomes in Males and Females with 46,XY Partial Gonadal Dysgenesis
Tadokoro-Cuccaro R., Hughes I. A., Cools M., Van De Vijver K., Bilharinho De Mendonça B., Domenice S., et al.
Journal of Clinical Endocrinology and Metabolism
, vol.110, no.12, 2025 (SCI-Expanded, Scopus)
2025
20254. Primary adrenal insufficiency caused by pseudo-neonatal adrenoleukodystrophy associated with biallelic ACOX1 mutations
Helvacioglu D., Canbaz A. T., Tekmenuray-Unal A., Ada Y., YAPICI Ö., Genc E., et al.
European Journal of Endocrinology
, vol.192, no.5, 2025 (SCI-Expanded)
2025
20255. Multi-Stakeholder Opinion Statement on the Care of Individuals Born with Differences of Sex Development: Common Ground and Opportunities for Improvement
Cools M., Cheng E. Y., Hall J., Alderson J., Amies Oelschlager A., Balen A. H., et al.
Hormone Research in Paediatrics
, vol.98, no.2, pp.226-242, 2025 (SCI-Expanded, Scopus)
2025
20256. Thyroid surgery in pediatric age: A ten-year experience at a single center and literature review
ASYA O., YUMUŞAKHUYLU A. C., GÜNDOĞDU Y., KUYUMCU Ö. F., DEMİRCİOĞLU S., GÜRAN T., et al.
Journal of Pediatric Endocrinology and Metabolism
, vol.38, no.3, pp.201-206, 2025 (SCI-Expanded)
2025
20257. Antenatal Diagnosis and Treatment in Congenital Adrenal Hyperplasia Due to 21-hydroxylase Deficiency and Congenital Adrenal Hyperplasia Screening in Newborns
Abalı Z. Y., KURNAZ E., GURAN T.
Journal of Clinical Research in Pediatric Endocrinology
, vol.17, no.1, pp.33-43, 2025 (SCI-Expanded, Scopus, TRDizin)
2025
20258. Gonadal function and pathology in 17beta-HSD 3 and 5alpha-reductase deficiency
Boogers L. S., Brüggenwirth H. T., Wolffenbuttel K. P., Hersmus R., Bryce J., Ahmed S. F., et al.
European Journal of Endocrinology
, vol.192, no.1, pp.34-45, 2025 (SCI-Expanded)
2024
20249. Rare forms of congenital adrenal hyperplasia
GÜRPINAR TOSUN B., GÜRAN T.
Clinical Endocrinology
, vol.101, no.4, pp.371-385, 2024 (SCI-Expanded)
2024
202410. Temporal Trends in Acute Adrenal Insufficiency Events in Children With Congenital Adrenal Hyperplasia During 2019-2022.
Tseretopoulou X., Ali S. R., Bryce J., Amin N., Atapattu N., Bachega T. A. S. S., et al.
Journal of the Endocrine Society
, vol.8, no.10, 2024 (ESCI, Scopus)
2024
202411. Assessment of prognostic factors in pediatric adrenocortical tumors: The modified pediatric S-GRAS score in an international multicenter cohort - A work from the ENSAT-PACT working group
Riedmeier M., Agarwal S., Antonini S., Costa T. E. B., Diclehan O., Fassnacht M., et al.
European Journal of Endocrinology
, vol.191, no.1, pp.64-74, 2024 (SCI-Expanded)
2024
202412. Evaluating breast ultrasonography as a complementary diagnostic method in girls with central precocious puberty
BIYIKLI E., Helvacıoğlu D., BUĞDAYCI O., Tosun B. G., DEMİRCİOĞLU S., GÜRAN T., et al.
Pediatric Radiology
, vol.54, no.7, pp.1156-1167, 2024 (SCI-Expanded, Scopus)
2024
202413. An Overlooked Manifestation of Hypercortisolism-Cerebral Cortical Atrophy and Challenges in Identifying the Etiology of Hypercortisolism: A Report of 2 Pediatric Cases
Eviz E., Mutlu G. Y., Akcay A. A., Erbey F., GÜRAN T., Hatun S.
HORMONE RESEARCH IN PAEDIATRICS
, vol.97, no.2, pp.172-179, 2024 (SCI-Expanded)
2024
202414. Bone Phenotype is Always Present But Androgen Excess is Less Frequently Seen in PAPSS2 Deficiency
Helvacıoğlu D., GURAN T.
Journal of Clinical Research in Pediatric Endocrinology
, vol.16, no.1, pp.4-10, 2024 (SCI-Expanded)
2024
202415. Development of external genitalia during mini-puberty: is it related to somatic growth or reproductive hormones?
Gacemer H. A., Tosun B. G., Helvacioglu D., Yaman A., Abali Z., HALİLOĞLU B., et al.
European journal of pediatrics
, vol.183, no.3, pp.1325-1332, 2024 (SCI-Expanded, Scopus)
2024
202416. Lack of NAD(P)+ transhydrogenase activity in patients with primary adrenal insufficiency due to NNT variants
Francisco A., Goler A. M., Navarro C. D. C., Onder A., Yildiz M., Demirkol Y. K., et al.
European Journal of Endocrinology
, vol.190, no.2, pp.130-138, 2024 (SCI-Expanded, Scopus)
2024
202417. Venous Thrombosis in a Pseudohypoparathyroidism Patient with a Novel GNAS Frameshift Mutation and Complete Resolution of Vascular Calcifications with Acetazolamide Treatment.
Menevse T. S., Iwasaki Y., Abali Z., Tosun B. G., Helvacioglu D., DOĞRU Ö., et al.
Hormone research in paediatrics
, vol.97, no.4, pp.404-415, 2024 (SCI-Expanded, Scopus)
2024
202418. Diagnosis and management of non-CAH 46,XX disorders/differences in sex development
Yavas Abalı Z., GÜRAN T.
Frontiers in Endocrinology
, vol.15, 2024 (SCI-Expanded, Scopus)
2023
202319. Hormonal control during infancy and testicular adrenal rest tumor development in males with congenital adrenal hyperplasia: a retrospective multicenter cohort study
Schröder M. A. M., Neacşu M., Adriaansen B. P. H., Sweep F. C. G. J., Ahmed S. F., Ali S. R., et al.
European journal of endocrinology
, vol.189, no.4, pp.460-468, 2023 (SCI-Expanded, Scopus)
2023
202320. Predictors of surgical complications in boys with hypospadias: Data from an internationa registry
Scougall K., Bryce J., Baronio F., Boal R. L., Castera J. R., Castro S., et al.
World Journal of Pediatric Surgery
, vol.6, no.4, 2023 (ESCI)
2023
202321. Challenges in the management of a 7 years old child with thyrotropin-secreting pituitary adenoma and the review of the literature
KIRKGÖZ T., Abali S., Seker A., GÜRPINAR TOSUN B., ELTAN M., Helvacioglu D., et al.
HORMONE RESEARCH IN PAEDIATRICS
, vol.96, no.5, pp.527-537, 2023 (SCI-Expanded, Scopus)
2023
202322. Pubertal and Gonadal Outcomes in 46,XY Individuals with Partial Androgen Insensitivity Syndrome Raised as Girls
Guaragna-Filho G., Guerra-Junior G., Tadokoro-Cuccaro R., Hughes I. A., Barros B. A., Hiort O., et al.
SEXUAL DEVELOPMENT
, vol.17, no.1, pp.16-25, 2023 (SCI-Expanded)
2023
202323. Decline in the Age of Menarche in Istanbul Schoolgirls Over the Last 12 Years.
GÜRAN T., HELVACIOĞLU D., TOSUN B. G., ABALI Z., Alır F., Arslan Y. t., et al.
Journal of clinical research in pediatric endocrinology
, vol.15, no.2, pp.154-159, 2023 (SCI-Expanded, Scopus, TRDizin)
2023
202324. Introduction.
Guran T., Flück C. E.
Hormone research in paediatrics
, vol.96, no.2, pp.115, 2023 (SCI-Expanded)
2023
202325. Molecular analysis of MKRN3 gene in Turkish girls with sporadic and familial idiopathic central
KIRKGÖZ T., KAYGUSUZ S. B., ALAVANDA C., Helvacioglu D., Abali Z., GÜRPINAR TOSUN B., et al.
JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM
, vol.36, no.4, pp.401-408, 2023 (SCI-Expanded, Scopus)
2023
202326. Evaluation of Cardiopulmonary Fitness and Cognitive Functions in Children with Obesity
Ozturk C. C., Toprakoglu H. S., Oruc F., Menevse T. S., Akbolat F. I., GÜRAN T., et al.
ACTA PHYSIOLOGICA
, vol.237, pp.30, 2023 (SCI-Expanded, Scopus)
2022
202227. Genotype of congenital adrenal hyperplasia patients with testicular adrenal rest tumor
AYCAN Z., Keskin M., Lafci N. G., Savas-Erdeve S., BAŞ F., POYRAZOĞLU Ş., et al.
EUROPEAN JOURNAL OF MEDICAL GENETICS
, vol.65, no.12, 2022 (SCI-Expanded)
2022
202228. [KS-015] İstanbul’da Yaşayan Kız Çocuklarında Son 12 Yılda Meydana Gelen Menarş Yaşı Değişiminin Belirlenmesi
Güran T.
XXVI. ULUSAL PEDİATRİK ENDOKRİNOLOJİ XXVI. VE DİYABET KONGRESİ , vol.1, no.1, pp.10, 2022 (Conference Book)
2022
202229. A homozygous Y443C variant in the RNPC3 is associated with severe syndromic congenital hypopituitarism and diffuse brain atrophy
Bezen D., Kutlu O., Mouilleron S., Rizzoti K., Dattani M., GÜRAN T., et al.
HORMONE RESEARCH IN PAEDIATRICS
, vol.95, no.SUPPL 2, pp.352-353, 2022 (SCI-Expanded)
2022
202230. 3 beta-Hydroxysteroid Dehydrogenase Deficiency, Rare in the Diagnosis of Congenital Adrenal Hyperplasia: A Case Report
Bulus A. D., Yasartekin Y., GÜRAN T.
HORMONE RESEARCH IN PAEDIATRICS
, vol.95, no.SUPPL 2, pp.449, 2022 (SCI-Expanded, Scopus)
2022
202231. Yenidoğanda Konjenital Adrenal Hiperplazi Taraması
Güran T.
Türkiye Klinikleri Pediatri Dergisi , no.1, pp.32-35, 2022 (Peer-Reviewed Journal)
2022
202232. P1-206 Primary adrenal insufficiency in a patient with biallelic QRSL1 mutations
Güran T.
HORMONE RESEARCH IN PAEDIATRICS , vol.95, no.2, pp.125, 2022 (SCI-Expanded)
2022
202233. Basal cortisol measurements in the prediction of low-dose ACTH stimulation test outcomes
Gacemer H., Gürpınar Tosun B., Abali Z. Y., Helvacioglu D., Haliloğlu B., Demircioğlu S., et al.
HORMONE RESEARCH IN PAEDIATRICS
, vol.95, no.SUPPL 2, pp.139, 2022 (SCI-Expanded)
2022
202234. Wide phenotypical spectrum with the same karyotype: Mixed gonadal dysgenesis
Seven Menevşe T., Gürpınar Tosun B., Helvacioglu D., Abali Z. Y., Kirmizibekmez H., Dursun F., et al.
HORMONE RESEARCH IN PAEDIATRICS
, vol.95, no.SUPPL 2, pp.566, 2022 (SCI-Expanded, Scopus)
2022
202235. Primary adrenal insufficiency in a patient with biallelic QRSL1 mutations
Dursun F., Genc H. M., Yılmaz Göler A. M., Tas I., Eser M., Pehlivanoglu C., et al.
EUROPEAN JOURNAL OF ENDOCRINOLOGY
, vol.187, no.3, 2022 (SCI-Expanded, Scopus)
2022
202236. Glucagon response to hypoglycemia during extended oral glucose tolerance test in children with cystic fibrosis and comparing with healthy peers
HALİLOĞLU B., SEVEN MENEVŞE T., GÜRPINAR TOSUN B., GÜRAN T., DEMİRCİOĞLU S., Ispir T., et al.
HORMONE RESEARCH IN PAEDIATRICS
, vol.95, no.SUPPL 2, pp.199-200, 2022 (SCI-Expanded, Scopus)
2022
202237. Differences due to the variant type in the inheritance pattern of BMP15 gene-related primary ovarian insufficiency: a girl with a homozygous null BMP15 gene variant
Abali Z. Y., Ates E. A., ELTAN M., GÜRPINAR TOSUN B., BEREKET A., GÜRAN T., et al.
HORMONE RESEARCH IN PAEDIATRICS
, vol.95, no.SUPPL 2, pp.377-378, 2022 (SCI-Expanded)
2022
202238. A homozygous Y443C variant in the RNPC3 is associated with severe syndromic congenital hypopituitarism and diffuse brain atrophy
Bezen D., Kutlu O., Mouilleron S., Rizzoti K., Dattani M., Güran T., et al.
AMERICAN JOURNAL OF MEDICAL GENETICS PART A
, vol.188, no.9, pp.2701-2706, 2022 (SCI-Expanded)
2022
202239. Circulating mRNA and miRNA Signatures as Predictive Markers of Lifestyle Modification Outcomes in Pediatric Obesity Treatment
Gawlik A., Shmoish M., BEREKET A., Wasniewska M., Antosz A., KIRKGÖZ T., et al.
HORMONE RESEARCH IN PAEDIATRICS
, vol.95, no.SUPPL 2, pp.213, 2022 (SCI-Expanded)
2022
202240. Gonadal morphology in 46,XY gonadal dysgenesis: I-DSD Registry-based study
Tadokoro-Cuccaro R., Hughes I., Cools M., van de Vijver K., de Mendonca B. B., Domenice S., et al.
HORMONE RESEARCH IN PAEDIATRICS
, vol.95, no.SUPPL 2, pp.44-45, 2022 (SCI-Expanded)
2022
202241. Diagnostic Features and Risk Factors for Childhood Thyroid Cancers
ŞAHİN P., GÜRPINAR TOSUN B., YUMUŞAKHUYLU A. C., GÜRAN T., Helvacioglu D., Abali Z. Y., et al.
HORMONE RESEARCH IN PAEDIATRICS
, vol.95, no.SUPPL 2, pp.407, 2022 (SCI-Expanded)
2022
202242. Change of menarcheal age in schoolgirls living in Istanbul over the last 12 years
Güran T., Alir F., Arslan Y. T., Molla G., Sahin B., Sayar M. E., et al.
HORMONE RESEARCH IN PAEDIATRICS
, vol.95, no.SUPPL 2, pp.364, 2022 (SCI-Expanded)
2022
202243. Gonadal morphology in 46,XY gonadal dysgenesis: I-DSD Registry-based study
Güran T.
HORMONE RESEARCH IN PAEDIATRICS , vol.95, no.Suppl 2, pp.44, 2022 (SCI-Expanded)
2022
202244. An International Study of the Association between Local Health Care Resources and Acute Adrenal Insufficiency Events in Children with Congenital Adrenal Hyperplasia
Tseretopoulou X., Ali S. R., Bryce J., Navoda A., Birkebaek N. H., Baronio F., et al.
HORMONE RESEARCH IN PAEDIATRICS
, vol.95, no.SUPPL 2, pp.401-402, 2022 (SCI-Expanded)
2022
202245. Breast ultrasonography: How useful in the diagnosis of precocious puberty?
Helvacioglu D., BIYIKLI E., BUĞDAYCI O., DEMİRCİOĞLU S., GÜRAN T., BEREKET A.
HORMONE RESEARCH IN PAEDIATRICS
, vol.95, no.SUPPL 2, pp.46-47, 2022 (SCI-Expanded)
2022
202246. Urinary steroid metabolite ratios: sex- and age-dependent changes and use for the differential diagnosis of inborn steroidogenesis disorders
Baranowski E. S., GÜRAN T., Gilligan L. C., Shaheen F., Utari A., Faradz S. M. H., et al.
HORMONE RESEARCH IN PAEDIATRICS
, vol.95, no.SUPPL 2, pp.114, 2022 (SCI-Expanded)
2022
202247. Low-dose ACTH Stimulation Test: Comparison of Cortisol Response at 30, 40, and 60 Minutes
Gürpınar Tosun B., Arıkan H., Demircioğlu S., Bereket A., Güran T.
HORMONE RESEARCH IN PAEDIATRICS
, vol.95, no.SUPPL 2, pp.117-118, 2022 (SCI-Expanded)
2022
202248. Etiological analysis of hypophosphatemia: A single-center experience
Eltan M., Alavanda C., Abali Z. Y., Bayramoglu E., Kaygusuz S. B., Helvacioglu D., et al.
HORMONE RESEARCH IN PAEDIATRICS
, vol.95, no.SUPPL 2, pp.141-142, 2022 (SCI-Expanded)
2022
202249. Predictors of surgical outcomes in boys with hypospadias
Scougall K., Bryce J., Baronio F., Boal R. L., Castera R., Castro S., et al.
HORMONE RESEARCH IN PAEDIATRICS
, vol.95, no.SUPPL 2, pp.376-377, 2022 (SCI-Expanded)
2022
202250. Single Nucleotide Polymorphisms (SNPs) Profile as Predictive Markers of Lifestyle Modification Outcomes in Pediatric Obesity Treatment
Gawlik A., Sobalska-Kwapis M., Antosz A., Strapagiel D., Seweryn M., Shmoish M., et al.
HORMONE RESEARCH IN PAEDIATRICS
, vol.95, no.SUPPL 2, pp.231-232, 2022 (SCI-Expanded, Scopus)
2022
202251. A rare cause of monogenic obesity: Schaaf-Yang syndrome due to a novel MAGEL2 gene variant
Abali Z. Y., Ates E. A., GÜRAN T., BEREKET A., DEMİRCİOĞLU S.
HORMONE RESEARCH IN PAEDIATRICS
, vol.95, no.SUPPL 2, pp.230, 2022 (SCI-Expanded, Scopus)
2022
202252. A retrospective analysis of endocrine disease in sphingosine-1-phosphate lyase insufficiency: case series and literature review
Maharaj A., Kwong R., Williams J., Smith C., Storr H., Krone R., et al.
ENDOCRINE CONNECTIONS
, vol.11, no.8, 2022 (SCI-Expanded)
2022
202253. Dysosteosclerosis: Clinical and Radiological Evolution Reflecting Genetic Heterogeneity
DEMİRCİOĞLU S., Mumm S., ALAVANDA C., Kaygusuz B. S., GÜRPINAR TOSUN B., ARMAN A., et al.
JBMR PLUS
, vol.6, no.8, 2022 (ESCI, Scopus)
2022
202254. Adrenal steroids reference ranges in infancy determined by LC-MS/MS
Enver E. O., Vatansever P., Guran O., Bilgin L., Boran P., Demircioğlu S., et al.
PEDIATRIC RESEARCH
, vol.92, no.1, pp.265-274, 2022 (SCI-Expanded, Scopus)
2022
202255. 46,XY Partial gonadal dysgenesis; diagnosis and long-term outcome at puberty
Cuccaro R. T., Hughes I., Cools M., van de Vijver K., de Mendonca B. B., Domenice S., et al.
SEXUAL DEVELOPMENT
, vol.16, no.SUPPL 1, pp.33-35, 2022 (SCI-Expanded)
2022
202256. Homozygosity for a novel INHA mutation in two male siblings with hypospadias, primary hypogonadism, and high normal testicular volume
Guran T., Ates E. A., Eltan M., Sahin B., Tosun B. G., Seven Menevşe T., et al.
SEXUAL DEVELOPMENT
, vol.16, no.SUPPL 1, pp.61-62, 2022 (SCI-Expanded)
2022
202257. Evaluation of thyroid function and metabolic parameters in obese and overweight children: A prospective case-control study.
Kartal A. T., Bozaykut A., Sezer R. G., Güran T.
INVESTIGACION CLINICA
, vol.63, no.2, pp.126-136, 2022 (SCI-Expanded)
2022
202258. Treatment of congenital adrenal hyperplasia in children aged 0-3 years: a retrospective multicenter analysis of salt supplementation, glucocorticoid and mineralocorticoid medication, growth and blood pressure
Neumann U., Van Der Linde A., Krone R. E., Krone N. P., Guven A., Güran T., et al.
EUROPEAN JOURNAL OF ENDOCRINOLOGY
, vol.186, no.5, pp.587-596, 2022 (SCI-Expanded)
2022
202259. Insights From Long-term Follow-up of a Girl With Adrenal Insufficiency and Sphingosine-1-Phosphate Lyase Deficiency
Maharaj A., Güran T., Buonocore F., Achermann J. C., Metherell L., Prasad R., et al.
JOURNAL OF THE ENDOCRINE SOCIETY
, vol.6, no.5, 2022 (ESCI)
2022
202260. Familial Hypomagnesemia with Hypercalciuria and Nephrocalcinosis Due to CLDN16 Gene Mutations: Novel Findings in Two Cases with Diverse Clinical Features
Eltan M., Abali Z., Turkyilmaz A., Gökce İ., Abali S., Alavanda C., et al.
CALCIFIED TISSUE INTERNATIONAL
, vol.110, no.4, pp.441-450, 2022 (SCI-Expanded, Scopus)
2022
202261. Steroid hormone profiles and molecular diagnostic tools in pediatric patients with non-CAH primary adrenal insufficiency.
Seven Menevse T., Kendir Demirkol Y., Gurpinar Tosun B., Bayramoglu E., Yildiz M., Acar S., et al.
The Journal of clinical endocrinology and metabolism
, vol.107, 2022 (SCI-Expanded, Scopus)
2022
202262. A novel deletion involving the first GNAS exon encoding Gsα causes PHP1A without methylation changes at exon A/B
Campbell D., Reyes M., Kaygusuz S. B., Abalı S., Güran T., Bereket A., et al.
Bone
, vol.157, 2022 (SCI-Expanded)
2022
202263. Homozygosity for a novel INHA mutation in two male siblings with hypospadias, primary hypogonadism, and high-normal testicular volume.
Arslan Ateş E., Eltan M., Sahin B., Gurpinar Tosun B., Seven Menevse T., Geckinli B. B., et al.
European journal of endocrinology
, vol.186, no.5, 2022 (SCI-Expanded, Scopus)
2022
202264. Efficacy of the Novel Degludec/Aspart Insulin Co-formulation in Children and Adolescents with Type 1 Diabetes: A Real-life Experience with 1-year IDeg/Asp Therapy in Poorly Controlled and Non-compliant Patients.
Kirkgoz T., Eltan M., Kaygusuz S. B., Yavas Abali Z., Helvacioglu D., Seven Menevse T., et al.
Journal of clinical research in pediatric endocrinology
, vol.14, pp.10-16, 2022 (SCI-Expanded, Scopus, TRDizin)
2022
202265. Systematic genetic testing for recessively inherited monogenic diabetes: a cross-sectional study in paediatric diabetes clinics
Patel K. A., Ozbek M. N., Yildiz M., GÜRAN T., Kocyigit C., ACAR S., et al.
DIABETOLOGIA
, vol.65, no.2, pp.336-342, 2022 (SCI-Expanded)
2022
202266. Catch-up growth and discontinuation of fludrocortisone treatment in aldosterone synthase deficiency.
Gurpinar Tosun B., Kendir Demirkol Y., Seven Menevse T., Kaygusuz S. B., Ozbek M. N., Altincik S. A., et al.
The Journal of clinical endocrinology and metabolism
, vol.107, 2022 (SCI-Expanded, Scopus)
2022
202267. Broad-spectrum XX and XY gonadal dysgenesis in patients with a homozygous L193S variant in PPP2R3C.
Cicek D., Warr N., Yesil G., Kocak Eker H., Bas F., Poyrazoglu S., et al.
European journal of endocrinology
, vol.186, pp.65-72, 2022 (SCI-Expanded, Scopus)
2021
202168. Non-hormonal Clitoromegaly due to Clitoral Priapism Caused by Appendicitis/Appendectomy.
Gurpinar Tosun B., Karagozlu Akgul A., Almus E., Abidoglu S., Turan S., Bereket A., et al.
Journal of clinical research in pediatric endocrinology
, no.4, 2021 (SCI-Expanded)
2021
202169. Dysgenesis and Dysfunction of the Pancreas and Pituitary Due to FOXA2 Gene Defects.
Kaygusuz S. B., Arslan Ates E., Vignola M. L., Volkan B., Geckinli B. B., Turan S., et al.
The Journal of clinical endocrinology and metabolism
, vol.106, no.10, 2021 (SCI-Expanded)
2021
202170. Is quail egg a potential endocrine disruptor?
Sürekli Karakuş Ö., Arabacı Tamer S., Levent H. N., Kaygusuz S. B., Demircioğlu S., Akakın D., et al.
HORMONE RESEARCH IN PAEDIATRICS
, vol.94, no.SUPPL 1, pp.364, 2021 (SCI-Expanded)
2009
200971. The exon 3 deleted/full length growth hormone receptor polymorphism and response to GH therapy in GH deficiency and Turner syndrome: a multicenter study
Darendeliler F. F., Bas F., Bozkurt N., Uzunhan O., Aycan Z., Cetinkaya E., et al.
HORMONE RESEARCH
, vol.72, pp.109, 2009 (SCI-Expanded)
2009
200972. A novel missense mutation in the first extracellular loop of the neurokinin B receptor causes hypogonadotropic hypogonadism
GÜRAN T., Tolhurst G., BEREKET A., Porter K., Turan S., Gribble F. M., et al.
HORMONE RESEARCH
, vol.72, pp.402, 2009 (SCI-Expanded)
Papers Presented at Peer-Reviewed Scientific Conferences
2024
20241. 10 YILLIK DENEYİM İLE PEDİATRİK POPÜLASYONDA TİROİD CERRAHİSİ
İSKANDARLİ E., ASYA O., YUMUŞAKHUYLU A. C., GÜNDOĞDU Y., OYSU Ç., KUYUMCU Ö. F., et al.
45. TÜRK ULUSAL KULAK BURUN BOĞAZ VE BAŞ BOYUN CERRAHİSİ KONGRESİ, Cyprus (Kktc), 23 - 27 October 2024, pp.98, (Summary Text)
2022
20222. Breast ultrasonography: How useful in the diagnosis of precocious puberty?
HELVACIOĞLU D., BIYIKLI E., BUĞDAYCI O., DEMİRCİOĞLU S., GÜRAN T., BEREKET A.
60th Annual Meeting of the European Society for Paediatric Endocrinology (ESPE), ROMA, Italy, 15 - 17 September 2022, (Summary Text)
2022
20223. DİYABETİN NADİR FORMU: MİTOKONDRİYAL DİYABET TANISINDA OLGULARLA YOL GÖSTERİCİ BULGULAR
Güran T.
ÇOCUK ENDOKRİNOLOJİSİ OLGU SUNUMLARI -11, İstanbul, Turkey, 13 - 15 May 2022, pp.90, (Full Text)
2022
20224. POSTTRANSPLANT HİPERGLİSEMİ: FARKLI SEYİR GÖSTEREN İKİ SİLİOPATİ OLGUSU
Güran T.
ÇOCUK ENDOKRİNOLOJİSİ OLGU SUNUMLARI -11, İstanbul, Turkey, 13 - 15 May 2022, pp.165, (Full Text)
2022
20225. NADİR BİR HİPOPİTUİTARİZM NEDENİ: MSS LENFOMASI
Güran T.
ÇOCUK ENDOKRİNOLOJİSİ OLGU SUNUMLARI -11-, 13 - 15 May 2022, pp.104, (Full Text)
2022
20226. DİYABETİN NADİR BİR NEDENİ, WERNER SENDROMU
Güran T.
ÇOCUK ENDOKRİNOLOJİSİ OLGU SUNUMLARI -11, İstanbul, Turkey, 13 - 15 May 2022, pp.59, (Full Text)
2022
20227. MONOGENİK OBEZİTENİN NADİR BİR NEDENİ: MAGEL2 GENİNDE YENİ TANIMLANMIŞ MUTASYON
Güran T.
ÇOCUK ENDOKRİNOLOJİSİ OLGU SUNUMLARI -11, İstanbul, Turkey, 13 - 15 May 2022, pp.89, (Full Text)
2022
20228. OBEZ ÇOCUKLARDA KARDİYOPULMONER EGZERSİZ TESTİ SONRASI AKUT OTONOMİK TOPARLANMA İLE DİNLENİK OTONOMİK REGÜLASYON İLİŞKİSİ
Toprakoğlu S., Çantalı Öztürk Ç., Oruç F., Seven Menevşe T., Akpolat F. İ., Güran T., et al.
8. EGZERSİZ FİZYOLOJİSİ SEMPOZYUMU, İstanbul, Turkey, 12 - 15 May 2022, pp.73-74, (Summary Text)
2022
20229. OBEZİTE PROBLEMİ OLAN ÇOCUKLARDA KARDİYOPULMONER SAĞLAMLIK VE KOGNİTİF FONKSİYON DEĞİŞİKLİKLERİ
Çantalı Öztürk Ç., Toprakoğlu S., Oruç F., Seven Menevşe T., Akpolat F. İ., Güran T., et al.
8. EGZERSİZ FİZYOLOJİSİ SEMPOZYUMU, İstanbul, Turkey, 12 - 15 May 2022, pp.53-54, (Summary Text)
2022
202210. EP-049 Nadir Bir Vaka: Adrenokortikal Kitle Kaynaklı Cushing Sendromu
Güran T.
9. Marmara Pediatri Kongresi, İstanbul, Turkey, 18 - 20 February 2022, pp.104, (Full Text)
2022
202211. EP-004 MATERNAL ANTİTİROİD İLAÇ KULLANIMINA BAĞLI KONJENİTAL GUATR OLGUSU
Güran T.
9. Marmara Pediatri Kongresi, İstanbul, Turkey, 18 - 20 February 2022, pp.72, (Full Text)
2022
202212. EP-001 Nadir Görülen Bir Tip 1 Diabetes Mellitus Komplikasyonu: Mauriac Sendromu
Güran T.
9. Marmara Pediatri Kongresi, İstanbul, Turkey, 18 - 20 February 2022, pp.70, (Full Text)
2021
202113. Türkiye`de Konjenital Adrenal Hiperplazi Yenidoğan Taraması: Verilerin Değerlendirilmesi
Güran T.
65. Türkiye Milli Pediatri Kongresi, Antalya, Turkey, 3 November - 07 December 2021, pp.1-2, (Full Text)
2021
202114. Optimizing medical therapy in congenital adrenal hyperplasia
Güran T.
Indonesian Congress of Pediatrics (KONIKA 2021), 15 October - 19 December 2021, pp.1-3, (Full Text)
2021
202115. Steroidogenezde Aberan Androjen Üretimi ve Klinik Yansımaları
Güran T.
XXV. Ulusal Pediatrik Endokrinoloji ve Diyabet Kongresi, Antalya, Turkey, 6 October - 10 December 2021, pp.1-3, (Full Text)
2021
202116. Common and rare adrenal causes of DSD
Güran T.
DSD SIG Programme , 08 October 2021, pp.1-2, (Full Text)
2021
202117. DNAJC3 Genindeki Bialelik Mutasyona Bağlı Hiperinsülinemik Hipoglisemi
Güran T., Gurpinar Tosun B., Turan S., Bereket A.
XXV. Ulusal Pediatrik Endokrinoloji & Diyabet Kongresi, Antalya, Turkey, 6 - 10 October 2021, pp.1-2, (Summary Text)
2021
202118. Toplumumuzda Osteogenezis İmperfektada Genetik Nedenler ve Genotip Fenotip İlişkisi
Kaygusuz S. B., Alavanda C., Eltan M., Seven Menevse T., Abalı S., Yavaş Abalı Z., et al.
XXV. Ulusal Pediatrik Endokrinoloji & Diyabet Kongresi, Antalya, Turkey, 06 October 2021, (Full Text)
2021
202119. Prematür adrenarş tanılı kız çocuklarında 11-oksiandrojenlerin klinik ve biyokimyasal parametrelerle ilişkisi.
Güran T., Yavas Abali Z., Turan S., Bereket A., Eltan M.
XXV. Ulusal Pediatrik Endokrinoloji & Diyabet Kongresi., Antalya, Turkey, 6 - 10 October 2021, pp.1-3, (Full Text)
2021
202120. Konjenital Adrenal Hiperplazi Tanısında Nadir Görülen 3 β-Hidroksisteroid Dehidrogenaz Eksikliği: Olgu Sunumu.
Güran T., Buluş A. D., Yaşartekin Y.
XXV. Ulusal Pediatrik Endokrinoloji & Diyabet Kongresi. , Antalya, Turkey, 6 - 10 October 2021, pp.1-2, (Full Text)
2021
202121. 46,XX cinsiyet gelisim bozukluklarina yaklasim
Güran T.
XXV. Ulusal Pediatrik Endokrinoloji ve Diyabet Kongresi, Antalya, Turkey, 6 - 10 October 2021, pp.2-3, (Full Text)
2021
202122. Toplumumuzda Osteogenezis İmperfektada Genetik Nedenler ve Genotip Fenotip İlişkisi.
Güran T., Kaygusuz S. B., Turan S., Bereket A.
XXV. Ulusal Pediatrik Endokrinoloji & Diyabet Kongresi. , Antalya, Turkey, 6 - 10 October 2021, pp.1-2, (Full Text)
2021
202123. Adrenokortikal hormon profilleri: KAH dışı primer adrenal yetmezlikte moleküler etiyolojiyi öngörebilir mi?
Seven Menevse T., GURPINAR TOSUN B., YILDIZ M., ORBAK Z., SÖBÜ E., ANIK A., et al.
XXV. Ulusal Pediatrik Endokrinoloji & Diyabet Kongresi, 06 October 2021, (Full Text)
2021
202124. Bıldırcın Yumurtası Bir Endokrin Bozucu mudur?
Güran T., Surekli Karakus O., Turan S., Bereket A., Yegen B.
XXV. Ulusal Pediatrik Endokrinoloji & Diyabet Kongresi, Antalya, Turkey, 6 - 10 October 2021, pp.1-3, (Summary Text)
2021
202125. Düşük Doz ACTH Uyarı Testinde 30, 40 ve 60. Dakikalardaki Kortizol Yanıtının Karşılaştırılması.
Güran T., Gurpinar Tosun B., Turan S., Bereket A.
XXV. Ulusal Pediatrik Endokrinoloji & Diyabet Kongresi. , Antalya, Turkey, 6 - 10 October 2021, pp.1-3, (Summary Text)
2021
202126. Adrenokortikal hormon profilleri: KAH dışı primer adrenal yetmezlikte moleküler etiyolojiyi öngörebilir mi?
Güran T., Seven Menevse T., Bereket A., Turan S.
XXV. Ulusal Pediatrik Endokrinoloji & Diyabet Kongresi. , Antalya, Turkey, 6 - 10 October 2021, pp.1-2, (Full Text)
2021
202127. Acetazolamide treatment in a patient with pseudohypoparathyroidism with venous calcification
SEVEN MENEVŞE T., GÜRPINAR TOSUN B., YAVAŞ ABALI Z., HELVACIOĞLU D., KAYGUSUZ S. B., ELTAN M., et al.
59th Annual European Society for Pediatric Endocrinology (ESPE) Conference, 22 - 26 September 2021, (Summary Text)
2021
202128. KONJENİTAL ADRENAL HİPERPLAZİNİN YÖNETİMİ
Güran T.
VI. Pediatrik Endokrinoloji İleri Kursu, İstanbul, Turkey, 11 - 13 June 2021, pp.1-3, (Full Text)
2021
202129. Optimizing medical therapy in different forms of CAH
Güran T.
Indian Society for Pediatric and Adolescent Endocrinology (ISPAE),Academics and Clinical Education Series (ISPAE - ACES), 29 - 30 May 2021, pp.1-2, (Full Text)
2021
202130. NADİR GÖRÜLEN BİR ADRENAL YETMEZLİK OLGUSU
Güran T., Şahin S. E., Emeksiz H.
10. OLGU SUNUMLARI , İzmir, Turkey, 9 - 10 April 2021, pp.1-2, (Full Text)
2021
202131. ADRENAL YETMEZLİK VE HİPERGONADOTROPİK HİPOGONADİZM BİRLİKTELİĞİ: P450SCC EKSİKLİĞİ.
Güran T., Şakar M., Erdeve Ş. S., Cetinkaya S.
10. OLGU SUNUMLARI, İzmir, Turkey, 9 - 10 April 2021, pp.1-2, (Full Text)
2021
202132. BOY KISALIĞI İLE BAŞVURAN KIRIK ÖYKÜSÜ OLMAYAN OSTEOGENEZİS İMPERFEKTA OLGUSU.
Güran T., Turan S., Kaygusuz S. B., Bereket A.
10. OLGU SUNUMLARI, İzmir, Turkey, 9 - 10 April 2021, pp.1-2, (Full Text)
2021
202133. NADİR BİR HİPERKALSEMİ NEDENİ: KONJENITAL LAKTAZ EKSİKLİĞİ.
Güran T., Turan S., Bereket A., Eltan M.
10. OLGU SUNUMLARI, İzmir, Turkey, 9 - 10 April 2021, pp.1-2, (Full Text)
2021
202134. NEONATAL DİYABETES MELLITUS İLE PREZENTE OLAN LRBA EKSİKLİĞİ: ABATACEPT DENEYİMİ.
Güran T., Gurpinar Tosun B., Turan S., Bereket A.
10. OLGU SUNUMLARI, İzmir, Turkey, 9 - 10 April 2021, pp.1-2, (Full Text)
2021
202135. EKTOPİK ACTH SENDROMLU 2 NADİR OLGU, 2 FARKLI PREZENTASYON.
Güran T., Hatun S., Yesiltepe Mutlu G.
10. OLGU SUNUMLARI, İzmir, Turkey, 9 - 10 April 2021, pp.1-2, (Full Text)
2021
202136. PSÖDOHİPOPARATİROİDİ TANILI HASTADA VENÖZ KALSİFİKASYON TEDAVİSİNDE ASETOZOLAMİD KULLANIMI.
Güran T., Turan S., Bereket A., Seven Menevse T.
10. OLGU SUNUMLARI, İzmir, Turkey, 9 - 10 April 2021, pp.1-2, (Full Text)
2021
202137. KLİTEROMEGALİNİN ENDER BİR NEDENİ: APENDEKTOMİ SONRASI GELİŞEN KLİTORAL PRİAPİSM.
Güran T., Turan S., Bereket A., Gurpinar Tosun B.
10. OLGU SUNUMLARI, İzmir, Turkey, 9 - 10 April 2021, pp.1-2, (Full Text)
2021
202138. 46, XY GONADAL DİSGENEZİLİ OLGUDA NR5A1 VE DHX37 GENLERİNDE DİGENİK MUTASYONLAR.
Güran T., Helvacioglu D., Turan S., Bereket A.
10. OLGU SUNUMLARI, İzmir, Turkey, 9 - 10 April 2021, pp.1-2, (Full Text)
2021
202139. Cocuklarda gecikmis puberte
Güran T.
Endokrinoloji Talim, Baku, Azerbaijan, 3 - 04 April 2021, pp.1-2, (Full Text)
2021
202140. PRİMER ADRENAL YETMEZLİK, KONJENİTAL NEFROTİK SENDROM VE HİPERGONADOTROPİK HİPOGONADİZM BİRLİKTELİĞİ: NADİR BİR OLGU.
Güran T., Bayram E., Aksu B.
4. Ege Endokrin Hastalıklar ve Genetik Sempozyumu. , İzmir, Turkey, 12 - 13 March 2021, pp.1-2, (Full Text)
2021
202141. PREPUBERTAL JİNEKOMASTİLİ OLGUDA AROMATAZ FAZLALIĞI.
Güran T., Eltan M., Turan S., Bereket A., Yavas Abali Z.
4. Ege Endokrin Hastalıklar ve Genetik Sempozyumu. , İzmir, Turkey, 12 - 13 March 2021, pp.1-2, (Summary Text)
2021
202142. OSTEOGENEZİS İMPERFEKTA ÖN TANISIYLA SEVK EDİLEN OLGUDA SAPTANAN NADİR BİR İSKELET DİSPLAZİSİ: KAMPOMELİK DİSPLAZİ.
Güran T., Seven Menevşe T., Turan S., Bereket A., Eltan M., Yavas Abali Z.
4. Ege Endokrin Hastalıklar ve Genetik Sempozyumu. , İzmir, Turkey, 12 - 13 March 2021, pp.1-2, (Full Text)
2021
202143. PRİMER ADRENAL YETMEZLİK, ASPLENİ, HİPOGONADOTROPİK HİPOGONADİZM: NR5A1 MUTASYONLU KIZ OLGUNUN YEDİ YILLIK İZLEMİ.
Güran T., Savas Erdeve S., Orman B., Aycan Z., Cetinkaya S.
4. Ege Endokrin Hastalıklar ve Genetik Sempozyumu. , İzmir, Turkey, 12 - 13 March 2021, pp.1-2, (Full Text)
2021
202144. MC2R MUTASYONLU SEKİZ OLGUNUN FENOTİPİK-GENOTİPİK ÖZELLİKLERİ
Güran T., Aycan Z., Esen S., Savas Erdeve S., Cetinkaya S.
4. Ege Endokrin Hastalıklar ve Genetik Sempozyumu., İzmir, Turkey, 12 - 13 March 2021, pp.1-2, (Full Text)
2021
202145. BMP15 GENİ İLE İLİŞKİLİ OVER DİSGENEZİSİNDE MUTASYON TİPİNE GÖRE KALITIM PATERNİ DEĞİŞİYOR MU?
Güran T., Turan S., Bereket A., Yavas Abali Z., Eltan M.
4. Ege Endokrin Hastalıklar ve Genetik Sempozyumu., İzmir, Turkey, 12 - 13 March 2021, pp.1-2, (Full Text)
2021
202146. Steroidogenezde Arka Yolak Hastalıklarının Klinik Yansımaları
Güran T.
4. Ege Endokrin Hastalıklar ve Genetik Sempozyumu, İzmir, Turkey, 12 - 13 March 2021, pp.1-2, (Full Text)
2021
202147. SLC29A3 MUTASYONUNA BAĞLI HASTALIK SPEKTRUMU: DİSOSTEOSKLEROZİSDEN H SENDROMUNA
Güran T., Kaygusuz S. B., Bereket A., Turan S., Yavas Abali Z.
4. Ege Endokrin Hastalıklar ve Genetik Sempozyumu. , İzmir, Turkey, 12 - 13 March 2021, pp.1-2, (Full Text)
2021
202148. Bıldırcın Yumurtası Bir Endokrin Bozucu Mudur?
Güran T., Surekli Karakus O., Turan S., Bereket A., Yegen B.
8. Marmara Pediatri Kongresi. , İstanbul, Turkey, 20 - 21 February 2021, pp.1-2, (Full Text)
2021
202149. Prader Willi Sendromlu Hastalarımızın Genetik, Endokrinolojik, Polisomnografik ve Otolaringolojik Değerlendirme Sonuçları
Seven Menevşe T., Baş S., Erdem Eralp E., Gürpınar Tosun B., Yavaş Abalı Z., Helvacıoğlu D., et al.
8. Marmara Pediatri Kongresi, İstanbul, Turkey, 20 February - 21 March 2021, pp.109-110, (Summary Text)
2021
202150. Konjenital Adrenal Hiperplazi Tanısında Zorluklar
Güran T.
Endokrin Hastalıkların Genetiği Seminerleri, İzmir, Turkey, 29 January 2021, pp.1-2, (Full Text)
2020
202051. 46, XX Cinsiyet gelişim bozukluklarına yaklaşım
Güran T.
VI. PEDİATRİK ENDOKRİNOLOJİYE GİRİŞ KURSU, İstanbul, Turkey, 21 - 22 November 2020, pp.1-2, (Full Text)
2020
202052. Steroid 11β-hidroksilaz eksikliği olan 100 çocuk hastanın klinik bulgularının genetik ve adrenokortikal hormonprofili ile ilişkisinin değerlendirilmesi
YILDIZ M., IŞIK E., TURAN S., KESKİN M., ÖZBEK M. N., BAŞ F., et al.
XXIV. Ulusal Pediatrik Endokrinoloji ve Diyabet Çevrim İçi Kongresi, Turkey, 30 October - 01 November 2020, pp.12, (Full Text)
2020
202053. Klasik tip 21 hidroksilaz eksikliğine bağlı konjenital adrenal hiperplazi tanılı olgularda puberte özellikleri,pubertal boy kazanımı ve final boya etki eden faktörlerin değerlendirilmesi: çok merkezli çalışma
YAVAŞ ABALI Z., YILDIZ M., BAŞ F., ÖNAL H., ABALI S., CİLSAAT G., et al.
XXIV.Ulusal Pediatrik Endokrinoloji ve Diyabet Çevrim İçi Kongresi, Turkey, 30 October - 01 November 2020, pp.34, (Full Text)
2020
202054. Steroid 11β-hidroksilaz eksikliği olan 100 çocuk hastanın klinik bulgularının genetik ve adrenokortikal hormon profili ile ilişkisinin değerlendirilmesi
YILDIZ M., DEMİRCİOĞLU S., KESKİN M., Özbek M. N., BEREKET A., GÜRAN T.
XXIV. Ulusal Pediatrik Endokrinoloji ve Diyabet Çevrim İçi Kongresi, Turkey, 30 October - 01 November 2020, (Full Text)
2020
202055. Geç tanı alan Turner sendromu olgusunda büyüme hormonu tedavisi ve puberte induksiyonu
Güran T.
NordiPEVA Büyüyen Tecrübe Toplantısı, İstanbul, Turkey, 27 October 2020, pp.1-2, (Full Text)
2020
202056. Adrenal Yetmezlik ve Yönetimi
Güran T.
Çocuk Endokrinolojisinde Güncellemeler, İstanbul, Turkey, 18 - 19 September 2020, pp.1-2, (Full Text)
2020
202057. ESPE DSD WG UPDATE
GÜRAN T.
I-DSD/CAH User Group Meeting, 9 September 2020 (webinar), United Kingdom, 09 September 2020, (Summary Text)
2020
202058. Endokrin Söyleşiler-Yeni Gen Keşfinde Yolculuk
Güran T.
24. Ulusal Pediatrik Endokrinoloji ve Diyabet Kongresi, İstanbul, Turkey, 15 - 19 April 2020, pp.1-2, (Full Text)
2019
201959. Exploring trends in the glucocorticoid and mineralocorticoid treatment of congenital adrenal hyperplasia by analysing data from the I-CAH registry
Bacilia I., Blankenstein O., Neumann U., Claahsen Van Der Grinten H., Krone R., Bachega T., et al.
47th Meeting of the British Society for Paediatric Endocrinology and Diabetes, Vienna, Austria, 27 - 29 November 2019, (Full Text)
2019
201960. Contemporary surgical approach in CAH 46XX – Results from the I-DSD/I-CAH Registries
Hebenstreit D., Faisal Ahmed S., Springer A., Krall C., Krone N., Birkebaek N., et al.
The 58th Annual ESPE Meeting, Vienna, Austria, 19 - 21 October 2019, (Full Text)
2019
201961. SGPL 1 deficiency leads to downregulation of key enzymes within the steroidogenic pathway
Avinaash M., Eirini M., Jack W., Güran T., Debora B., Louise M., et al.
ESPE 2019, Vienna, Austria, 19 - 21 September 2019, (Full Text)
2019
201962. Rare Causes of Osteogenesis Imperfecta are Commonin Consanguineous Pedigrees
KAYGUSUZ S. B., ARMAN A., ABALI S., ATA P., KIRKGÖZ T., YAVAŞ ABALI Z., et al.
European Society for Paediatric Endocrinology (ESPE)58th Annual Meeting, Vienna, VİYANA, Austria, 19 - 21 September 2019, (Full Text)
2019
201963. A rare cause of hypophosphatemia: Raine Syndrome
ELTAN M., ATA P., KIRKGÖZ T., ALAVANDA C., KAYGUSUZ S. B., SEVEN M. T., et al.
European Society for Paediatric Endocrinology (ESPE)58th Annual Meeting, Vienna, VİYANA, Austria, 19 - 21 September 2019, vol.91, (Full Text)
2019
201964. A Case Of Syndromic Hypopituitarism
KAYGUSUZ S. B., Arslan Ateş E., KIRKGÖZ T., ELTAN M., YAVAŞ ABALI Z., Helvacioglu D., et al.
European Society for Paediatric Endocrinology (ESPE)58th Annual Meeting, Vienna, 19 - 21 September 2019, vol.91, pp.1-682, (Summary Text)
2019
201965. Genotype and Phenotype Characterization ofTurkish Patients with Vitamin D Dependent RicketsType IA
KAYGUSUZ S. B., ATA P., KIRKGÖZ T., YAVAŞ ABALI Z., ELTAN M., GÜRPINAR T. B., et al.
European Society for Paediatric Endocrinology (ESPE)58th Annual Meeting, Vienna, VİYANA, Austria, 19 - 21 September 2019, vol.91, (Full Text)
2019
201966. PPP2R3C Gene Variants Cause Syndromic 46,XY Gonadal Dysgenesis and Impaired Spermatogenesis in Human
Güran T.
7th I-DSD Symposium, Sao-Paulo, Brazil, 4 - 06 July 2019, (Full Text)
2019
201967. Segmental Aşırı büyüme kliniği olan olguda somatik PIK3CA mutasyonu
Yavaş Abalı Z., Arslan Ateş E., Türkyılmaz A., Salman A., Kırkgöz T., Kaygusuz S. B., et al.
3. Ege Endokrin Hastalıklar ve Genetik Sempozyumu, İzmir, Turkey, 7 - 09 March 2019, (Full Text)
2019
201968. 40 Günlük Olguda Ambulatuar Kan Basıncı Ölçümü
Sak M., Kırkgöz T., Sağlam C., Arslan S., Güran T., Gökce İ., et al.
6. Marmara Pediatri Kongresi, İstanbul, Turkey, 21 - 23 February 2019, pp.207, (Summary Text)
2018
201869. A further case of autosomal recessive brachyolmia having a novel mutation in PAPSS2 gene
Arslan Ateş E., Eltan M., Türkyılmaz A., Alavanda C., Söylemez M. A., Geçkinli B. B., et al.
13 ULUSAL TIBBİ GENETİK KONGRESİ, Antalya, Turkey, 7 - 11 November 2018, (Full Text)
2018
201870. Düşük renin düzeyi: endokrin hipertansiyon
abalı Z., ABALI S., KÜÇÜK N., CANPOLAT N., ÇİÇEK N., ALPAY H., et al.
Çocuk Endokrinolojisi Olgu Sunumları-9, İstanbul, Turkey, 19 - 20 October 2018, (Full Text)
2018
201871. Düşük renin düzeyi: endokrin hipertansiyon
Abalı Z., Abalı S., Küçük N., Canpolat N., Çiçek Deniz N., Alpay H., et al.
Çocuk Endokrinolojisi Olgu Sunumları-9, İstanbul, Turkey, 19 - 20 October 2018, (Full Text)
2018
201872. Nationwide Hypophosphatemic Rickets Study
ŞIKLAR Z., TURAN S., BEREKET A., ABACI A., BAŞ F., DEMİR K., et al.
57.th Annual Meeting of the European Society for Paediatric Endocrinology(ESPE), ATİNA, Greece, 27 - 29 September 2018, (Summary Text)
2018
201873. Comprehensive Genetic Testing Shows One in FiveChildren with Diabetes and Non-Autoimmune Extra-Pancreatic Features Have Monogenic Aetiology.
Kashyap P., Colclough K., Özbek M. N., Yıldız M., Güran T., Koçyiğit C., et al.
57th Annual Meeting of the ESPE, Athens, Greece, 27 - 29 September 2018, (Summary Text)
2018
201874. Presenting Features, Clinical Characteristics andFollow Up of Familial Isolated GlucocorticoidDeficiency (FGD) Due to Mutations in MC2R andMRAP Genes
Ozbek M. N., Doğan Karaşin N., Demirbilek H., Demiral M., Baran R. T., Güran T.
57th Annual Meeting of ESPE (European Society for Pediatric Endocrinology, Athens, Greece, 27 - 29 September 2018, (Summary Text)
2018
201875. Persistan Mullerian Duct Syndrome: Rare but impotant aetiology of an inguinal hernia and cryptorchidism in boys
Bereket A., Buğrul F., Kırkgöz T., Karadeniz Cerit K., Canmemiş A., Turan S., et al.
57th Annual European Society for Paediatric Endocrinology(ESPE), Athens, Greece, 27 - 29 September 2018, (Summary Text)
2018
201876. Persistent Mullerian duct syndrome: Rare But Important Aetiology of an Inguinal Hernia and Cryptorchidism in Boys
BEREKET A., BUGRUL F., KIRKGÖZ T., KARADENİZ CERİT K., CANMEMİS A., DEMİRCİOĞLU S., et al.
HORMONE RESEARCH IN PAEDIATRICS-57th Annual Meeting of the European Society for Paediatric Endocrinology, 27 - 29 September 2018, vol.90, pp.568, (Full Text)
2018
201877. Isolated Congenital Central Hypothyroidism due to a Novel Mutation in TSH Beta Subunit Gene
Kırkgöz T., Özhan B., Çetin G. O., Kaygusuz S. B., Demircioğlu S., Bereket A., et al.
HORMONE RESEARCH IN PAEDIATRICS-57th Annual Meeting of the European Society for Paediatric Endocrinology, Athens, Greece, 27 - 29 September 2018, vol.90, pp.597, (Full Text)
2018
201878. Recurrent Hypoglycemia in a Preschooler Girl with Overgrowth: Isolated ACTH-Deficiency with a Novel TPIT Mutation
Yavaş Abalı Z., Yeşil G., Kırkgoz T., Kaygusuz S. B., Demircioğlu S., Bereket A., et al.
HORMONE RESEARCH IN PAEDIATRICS, Athens, Greece, 27 - 29 September 2018, vol.90, pp.132, (Full Text)
2018
201879. Neonatal screening for congenital adrenal hyperplasia in Turkey: A pilot study with 38935 infants
Güran T., Tezel B., Gürbüz F., Selver Eklioğlu B., Hatipoğlu N., Kara C., et al.
57th Annual Eurepean Society for Pediatric Endocrinology, Athens Greece, Athens, Greece, 27 - 29 September 2018, (Summary Text)
2018
201880. Evaluation of molecular characteristics and steroid metabolomics in a large cohort of children with 3β-Hydroxysteroid Dehydrogenase 2 deficiency.
GÜRAN T., KARA C., yildiz m., bitkin e. c., guven a., catli g., et al.
The 18th Adrenal cortex conference, 25 - 27 June 2018, (Full Text)
2018
201881. Kolesterolden Pregnenolona Dönüşümde Rol Alan Genlerin (StAR, CYP11A ve NNT) Mutasyonuna Bağlı Primer Adrenal Yetmezlik: Klinik Özellikler ve İzlem
Özbek M. N., Demirbilek H., Demiral M., Karaşin N. D., Baran R. T., Güran T.
22. Ulusal Pediatrik Endokrinoloji ve Diyabet Kongresi, Antalya, Turkey, 18 - 22 April 2018, (Summary Text)
2018
201882. Türkiyede Konjenital Adrenal Hiperplazi Yenidoğan Taraması
Güran T., Tezel B., Gürbüz F., Selver Eklioğlu B., Hatipoğlu N., Kara C., et al.
XXII. Ulusal Pediatrik Endokrinoloji ve Diyabet Kongresi, Antalya, Turkey, 18 - 22 April 2018, (Summary Text)
2018
201883. MC2R ve MRAP Gen Mutasyonuna Bağlı Familal Glukortikoid Direnci Olgularının Başvuru Özellikleri, Klinik ve İzlem
Özbek M. N., Karaşin N. D., Demirbilek H., Demiral M., Kavurt S., Baran R. T., et al.
22. Ulusal Pediatrik Endokrinoloji ve Diyabet Kongresi, Antalya, Turkey, 18 - 22 April 2018, (Summary Text)
2018
201884. Çok Merkezli Olarak Hipofosfatemik Riketsli Olguların Değerlendirilmesi
ŞIKLAR Z., TURAN S., BEREKET A., ABACI A., GÜRAN T., DEMİR K., et al.
22. PEDİATRİK ENDOKRİNOLOJİ VE DİYABET KONGRESİ, Antalya, Turkey, 18 - 22 April 2018, (Summary Text)
2018
201885. 21 HİDROKSİLAZ EKSİKLİĞİNE BAĞLI KLASİK OLMAYAN KONJENİTAL ADRENAL HİPERPLAZİDE KLİNİK, LABORATUVAR, GENETİK ÖZELLİKLER, TEDAVİYE ALINAN YANITLAR VE ULAŞILAN FİNAL BOY VERİLERİ
Savaş Erdeve Ş., Çetinkaya S., Yavaş Abalı Z., Poyrazoğlu Ş., Baş F., Berberoğlu M., et al.
22. PEDİATRİK ENDOKRİNOLOJİ VE DİYABET DERNEĞİ, Antalya, Turkey, 18 - 22 April 2018, (Summary Text)
2018
201886. Türkiye`de Konjenital Adrenal Hiperplazi Yenidoğan Taraması: 38.936 Bebeği Kapsayan Pilot Çalışma Verilerinin Değerlendirilmesi
Güran T., Tezel B., Gürbüz F., Selver Eklioğlu B., Hatipoğlu N., Kara C., et al.
XXII. Ulusal Pediatrik Endokrinoloji ve Diyabet Kongresi, Antalya, Turkey, 18 - 22 April 2018, (Summary Text)
2017
201787. Characteristics in 5-Alpha Reductase Type 2 Deficiency: A Multicenter Study from Turkey.
Abacı A., Çatlı G., Kırbıyık Ö., Şahin N. M., Abalı Z. Y., Ünal E., et al.
10th International Meeting of Pediatric Endocrinology, Washington, United States Of America, 10 - 17 September 2017, (Summary Text)
2017
201788. 17OH-PREGNENOLONE SEEMS A MAJOR DRIVE OF ANDROGEN EXCESS IN PATIENTS WITH 11ß-HYDROXYLASE DEFICIENCY
Yildiz M., Turan S., Akcay T., Atay Z., Onal H., Baris T., et al.
. 10th Individual Abstracts for International Meeting of Pediatric Endocrinology, Washington, United States Of America, 14 - 17 September 2017, (Full Text)
2017
201789. MAPPING THE STEROID METABOLOME IN INBORN STEROIDOGENIC DISORDERS: PERFORMANCE OF A NOVEL COMPUTATIONAL APPROACH IN COMPARISON TO CONVENTIONAL GC-MS ANALYSIS.
Baranowski E. S., Kerstin B., Shackleton C. H., Taylor A. E., Hughes B. A., Biehl M., et al.
10th Individual Abstracts for International Meeting of Pediatric Endocrinology, Washington, United States Of America, 14 - 17 September 2017, (Full Text)
2017
201790. SIMULTANEOUS PROFILING OF 17 STEROID HORMONES USING LIQUID CHROMATOGRAPHY TANDEM MASS SPECTROMETRY IN NEWBORN AND EARLY INFANCY.
Enver E. Ö., Vatansever P., Guran O., Boran P., Turan S., Haklar G., et al.
10th Individual Abstracts for International Meeting of Pediatric Endocrinology, Washington, United States Of America, 14 - 17 September 2017, (Full Text)
2017
201791. CYP11A1 mutations Results Various Clinical Phenotypes.
Güven A., Buonocore F., Achermann J., Güran T.
10th International Meeting of Pediatric Endocrinology, Washington, United States Of America, 14 - 17 September 2017, (Summary Text)
2017
201792. 17-Hydroxlase deficiency: Rare Cause of Delayed Puberty
Güven A., Güran T., Krone N.
10th International Meeting of Pediatric Endocrinology, Washington, United States Of America, 14 - 17 September 2017, (Summary Text)
2017
201793. 17OH-pregnenolone seems a major drive of androgen excess in patient with 11 beta hydroxylase deficiency
Yıldız M., TURAN S., Akçay T., Atay Z., ÖNAL H., Barış T., et al.
10th Joint Meeting of Paediatric Endocrinology, Washington, Kiribati, 14 - 17 September 2017, vol.88, pp.54, (Summary Text)
2017
201794. aldosterone synthase deficiency: a new mutation
Döğer E., Kılınç Uğurlu A., Kazancıoğlu A., Demet Akbaş E., Güran T., Bideci A., et al.
10. İnternational meeting of pediatric endocrinology, Washington, United States Of America, 14 - 17 September 2017, (Summary Text)
2017
201795. The prevalence of adults with SDS conditions at risk of hypogonadism in the international disorders of sex development registry
Lucas Herald A. K., Kyriakou A., Bryce J., Martina R., Carlo A., Arlt W., et al.
10 th International Meeting of Pediatric Endocrinology, Washington, United States Of America, 14 - 17 September 2017, (Summary Text)
2017
201796. familial glucocortıcoid deficiency type 2: a new mutation in the mrap gene p. k30del
Bideci A., Döğer E., Demet Akbaş E., Kılınç Uğurlu A., Güran T., Çamurdan M. O., et al.
10. international meeting of pediatric endocrinology, Washington, United States Of America, 14 - 17 September 2017, (Summary Text)
2017
201797. CLINICAL AND LABORATORY CHARACTERISTICS OF HYPERPROLACTINEMIC CHILDREN AND ADOLESCENTS: NATIONAL SURVEY.
EREN E., ERGÜR A., İŞGÜVEN Ş. P., ÇELEBİ BİTKİN E., BERBEROĞLU M., ŞIKLAR Z., et al.
IMPE 2017, 14 - 17 September 2017, (Summary Text)
2017
201798. PHENOTYPIC, HORMONAL AND MOLECULAR GENETIC CHARACTERISTICS OF 5-ALPHA REDUCTASE TYPE 2 DEFICIENCY PATIENTS: A MULTICENTER STUDY FROM TURKEY.
Abacı A., Çatlı G., Kırbıyık Ö., Şahin N., Yavaş Abalı Z., Ünal E., et al.
IMPE 2017, Washington, United States Of America, 14 - 17 September 2017, (Summary Text)
2017
201799. Defining the dose, type and timing of glucocorticoid and mineralocorticoid replacement in 256 children and adults with CAH in the I-CAH registry
Daniel E., Sandrk M., Blankenstein O., Neumann U., Grinten H., Linde A., et al.
10th International Meeting Of Pediatric Endocrinology, Washington, United States Of America, 14 - 17 September 2017, (Summary Text)
2017
2017100. A Rare Endocrine Cause of Hypertension: Apparent Mineralocorticoid Access Syndrome
Küçük N., Canpolat N., Akın Y., Meriç İ., Esmi E., Özçelik G. Ş., et al.
50th Anniversary Meeting of the European Society For Paediatric Nephrology.SEC Glasgow., Glasgow, United Kingdom, 6 - 09 September 2017, vol.32, pp.1744, (Summary Text)
2017
2017101. Evaluation of Clinical, Genetical, and Steroid Profile Features of Cases with 3Beta-Hydroxysteroid Dehydrogenase Type 2 Deficiency
Güran T., Kara C., Atay Z., Akbarzade A., Yılmaz G., Çelebi Bitkin E., et al.
American Association of Clinical Chemistry Congress, Washington, United States Of America, 30 July - 03 August 2017, (Full Text)
2017
2017102. Characterisation of adults at risk of long-term, early onset hypogonadism In the International Disorders of Sex Development Registry
Lucasherald A., Kyriakou A., Bryce J., Rodie M., C A., Arlt W., et al.
6th International Symposium Disorders of Sex Development., Washington, United States Of America, 29 June - 01 July 2017, (Full Text)
2017
2017103. Steroid metabolomics for accurate and rapid diagnosis of inborn steroidogenic disorders
Baranowski E., Bunte K., Shackleton C. H. L., Taylor A. E., Hughes B. A., Biehl M., et al.
19th European Congress of Endocrinology., Washington, United States Of America, 20 - 23 May 2017, (Full Text)
2017
2017104. 5 alfa redüktaz tip2 eksikliği tanılı olguların fenotipik hormonal ve moleküler genetik özellikleri: çok merkezli ulusal veriler
Abacı A., Çatlı G., Kırbıyık Ö., Muratoğlu Şahin N., Abalı Z. Y., Ünal E., et al.
21. Ulusal Pediatrik Endokrin Diyabet Kongresi, Antalya, Turkey, 26 - 30 April 2017, (Summary Text)
2017
2017105. Aldosteron sentaz eksikliği: yeni bir mutasyon
Kılınç Uğurlu A., Döğer E., Kazancıoğlu A., Demet Akbaş E., Güran T., Bideci A., et al.
21. ulusal pediatrik endokrinoloji ve diyabet kongresi, Antalya, Turkey, 26 - 30 April 2017, (Summary Text)
2017
2017106. Ailevi glukokortikoid eksikliği tip 2: MRAp geninde yeni mutasyon p.K30del
Döğer E., Demet Akbaş E., Kılınç Uğurlu A., Güran T., Bideci A., Çamurdan M. O., et al.
21. ulusal pediatrik endokrinoloji ve diyabet kongresi, Antalya, Turkey, 26 - 30 April 2017, (Summary Text)
2017
2017107. Mutations in SGPL1, causing sphingosine-1-phosphate lyase deficiency, cause a novel form of primary adrenal insufficiency with steroid resistant nephrotic syndrome.
Prasad R., Hadjidemetriou I., Avinaash M. A., Meimaridou E., Van Veldhoven P., Buonocore F., et al.
ENDO 2017, Washington, United States Of America, 1 - 04 April 2017, (Full Text)
2012
2012108. Çocukluk çağındaki over kisti vakalarının incelenmesi: çok merkezli çalışma
Küçükemre Aydın B., Saka N., BAŞ F., POYRAZOĞLU Ş., BUNDAK R., YEŞİLTEPE MUTLU R. G., et al.
16. Ulusal Pediatrik Endokrinoloji Kongresi, Turkey, 8 - 10 November 2012, (Summary Text)
2016
2016109. LC MSMS cihazı ile steroid hormon analizi ve klinik sonuçları
Yaman A., Güran T., Şirikçi Ö., Haklar G.
Klinik Biyokimya Uzmanları Derneği Kongresi ve Lab Expo 2016, Antalya, Turkey, 27 September - 01 October 2016, (Full Text)
2016
2016110. Mutations in SGPL1 cause a novel form of primary adrenal insufficiency with steroid resistant nephrotic syndrome
Prasad R., Hadjidemetriou I., Avinaash M. A., Meimaridou E., Van Veldhoven P., Buonocore F., et al.
55.TH ESPE-Paris-France, 10-12 September, Paris, France, 10 - 12 September 2016, (Full Text)
2016
2016111. A Multicenter Study on Long Term Outcomes in 56 Males with 45 X 46 XY Mosaicism
Lindhardt Johansen M., Acerini C., Andrade J., Balsamo A., Cools M., Cools M., et al.
55.TH ESPE-Paris-France, 10-12 September, 10 - 12 September 2016, (Full Text)
2016
2016112. A New International Registry Highlights the Differences in Practice for Reaching a Diagnosis of CAH On Behalf of the I CAH I DSD Registry User Group
Kourime M., Bryce J., Jiang J., Karunasena N., GÜRAN T., Hannema S. E., et al.
55.TH ESPE-Paris-France, 10-12 September, 10 - 12 September 2016, (Full Text)
2016
2016113. A Novel Animal Model to Study 21 Hydroxylase Deficiency in vivo
Zaucker A., Griffin A., Storbeck K., Güran T.
HORMONE RESEARCH IN PAEDIATRICS, 55.TH ESPE-Paris-France, 10-12 September, Paris, France, 10 - 12 September 2016, (Full Text)
2016
2016114. b hCG from an Occult Source Causing Peripheral Precocious Puberty Identification of the Tumour 6 Years After Presentation
Ekberzade A., Abalı S., Atay Z., Bas S., Gurbanov Z., Turan S., et al.
55.TH ESPE-Paris-France, 10-12 September, Paris, France, 10 - 12 September 2016, (Full Text)
2016
2016115. Precocious Puberty in Patients with Primary Adrenal Insufficiency due to Melanocortın Receptor 2 Mutation
Bas F., Abali Z. Y., Güran T., Genens M., Poyrazoglu S., Bundak R., et al.
55.TH ESPE-Paris-France, 10-12 September, Paris, France, 10 - 12 September 2016, (Full Text)
2016
2016116. Mutations in SGPL1 the Gene Encoding Sphingosine 1 Phosphate Lyase Cause a Novel Form of Primary Adrenal Insufficiency with Steroid Resistant Nephrotic Syndrome
Prasad R., Hadjidemetriou I., Avinaash M. A., et a., Braslavsky D., GÜRAN T., et al.
HORMONE RESEARCH IN PAEDIATRICS, 55.TH ESPE-Paris-France, 10-12 September, 10 September 2016, (Full Text)
2016
2016117. Thiamine Responsive Megaloblastic Anemia Due to SLCA19A2 Gene Mutation Another Cause of Neonatal Diabetes with Succcesfull Switch from Insulin to Thiamine
BAŞ S., Akbarzade A., ATAY Z., Gurbanov Z., GÜRAN T., TURAN S., et al.
55th Annual Meeting of the ESPE, 10 - 12 September 2016, vol.86, pp.244, (Summary Text)
2016
2016118. Etiologic Distribution and Characteristics of Patients with Short Stature in a Pediatric Endocrinology Clinic
Ozcan S., ABALI S., ATAY Z., Haliloğlu B., BAŞ S., Öztürk G., et al.
55th Annual Meeting of the ESPE, 10 - 12 September 2016, vol.86, pp.457-458, (Summary Text)
2016
2016119. beta hCG from an Occult Source Causing Peripheral Precocious Puberty Identification of the Tumour 6 Years After Presentation
Ekberzade A., ABALI S., BAŞ S., ATAY Z., Gurbanov Z., TURAN S., et al.
55th Annual Meeting of the ESPE, 10 - 12 September 2016, vol.86, pp.428, (Summary Text)
2016
2016120. Reconsideration of Mid Parental Height Calculation
BEREKET A., Bugur I. S., GÜRAN T., ATAY Z., Ekberzade A., Gurbanov Z., et al.
55th Annual Meeting of the ESPE, 10 - 12 September 2016, vol.86, pp.451, (Summary Text)
2016
2016121. Frequency of Recessive Osteogenesis Imperfecta in a Turkish Cohort and Genetic Causes
ABALI S., ARMAN A., ATAY Z., BEREKET A., BAŞ S., Haliloğlu B., et al.
55th Annual Meeting of the ESPE, Paris, 10 - 12 September 2016, vol.86, pp.175-176, (Summary Text)
2016
2016122. Steroid metabolomics for diagnosis of inborn steroidogenic disorders bridging the gap between biochemist and clinician through computational approaches
Baranowski E. S., Bunte K., Shackleton C. H., Taylor A. E., Hughes B. A., Biehl M., et al.
SfE British Endocrine Society, Edinburgh, United Kingdom, 7 - 09 September 2016, (Full Text)
2016
2016123. Premature Puberche Hyperinsülinemia Hypothyroxenemia and Hyperintensities in Basal Ganglia All Caused by a Single Congenital Defect
BAŞ S., GÜRAN T., ATAY Z., Haliloğlu B., ABALI S., TURAN S., et al.
Current Trends in Pediatric Endocrinology- A, 13 - 14 May 2016, (Full Text)
2016
2016124. Adrenal crisis and sick day episodes among CAH patients preliminary report based on International CAH I CAH registry
Karunasena N., Daniel E., Bryce J., Jiang J., S Faisal A., Güran T., et al.
18th European Congress of Endocrinology meeting, Munich, 28-31 May 2016, Munich, Germany, 28 - 31 May 2016, (Full Text)
2016
2016125. Premature Pubarche Hyperinsulinemia Hypothyroxinemia and Hyperintensities in Basal Ganglia All Caused by a Single Congenital Defect
Bas S., Güran T., Atay Z., Halıloglu B., Abalı S., Turan S., et al.
Current Trends in Pediatric Endocrinology- A PES perspective, İstanbul, Turkey, 13 - 14 May 2016, (Full Text)
2015
2015126. Zebra baliginda zCyp21a2 geninin karakterizasyonu
Güran T., Zaucker A., Taylor A., Doultsinos D., Griffin A., Mueller F., et al.
XIX. Ulusal Pediatrik Endokrinoloji, İstanbul, Turkey, 22 - 25 October 2015, (Full Text)
2015
2015127. Periferal Puberte Prekokslu 129 Çocukta Etiyolojik Dağılım Ve Klinik Özellikler
Atay Z., Yeşilkaya E., Savaş Ş., Turan S., Akın L., Eren E., et al.
19. Ulusal Pediatrik Endokrinoloji ve Diyabet Kongresi, Antalya, Turkey, 22 - 24 October 2015, (Full Text)
2015
2015128. 5 Reduktaz tip 2 eksikligine yol acan yeni mutasyonlarin molekuler karakterizasyonu
Güran T., Shafqat N., Taylor A., Bujalska I., Ivison H., Wiebke A.
XIX. Ulusal Pediatrik Endokrinoloji ve Diyabet Kongresi, İstanbul, Turkey, 22 - 25 October 2015, (Full Text)
2015
2015129. Boy Kısalığı Olan Hastalarda Özellikler ve Etiyolojik Dağılım Bir Çocuk Endokrinoloji Kliniği Verileri
Özcan S., Abalı S., Atay Z., Haliloğlu B., Baş S., Öztürk G., et al.
19. Ulusal Pediatrik Endokrinoloji ve Diyabet Kongresi, Antalya, Turkey, 22 - 24 October 2015, (Summary Text)
2015
2015130. Otozomal Resesif Osteogenezis İmperfekta Populasyonumuzdaki Sıklığı Ve Genetik Nedenleri
ABALI S., ARMAN A., ATAY Z., BAŞ S., GÜRAN T., GÖRMEZ Z., et al.
19. PEDİATRİK ENDOKRİNOLOJİ VE DİYABET KONGRESİ, Turkey, 22 - 24 October 2015, (Full Text)
2015
2015131. 5 Reduktaz tip 3 eksikliginin insan steroid metabolizmasina etkisi
Güran T., Bas F., Gokcay G., Hughes B. A., Kayserili Karabey H., Shackleton C. H., et al.
XIX. Ulusal Pediatrik Endokrinoloji ve Diyabet Kongresi, İstanbul, Turkey, 22 - 25 October 2015, (Full Text)
2015
2015132. Merkezi Yenidogan Tarama Programi ile Tani Almis Konjenital Hipotiroidili Vakalarimizin İzlemi
Baş S., Abalı S., Atay Z., Gurbanov Z., Haliloglu B., Güran T., et al.
19. Ulusal Pediatrik Endokrinoloji ve Diyabet Kongresi, Antalya, Turkey, 22 - 24 October 2015, (Summary Text)
2015
2015133. Nonklasik Konjenital Adrenal Hiperplazi Hastalarının Genotip Ve Fenotip Özellikleri
Abalı S., Akcan N., Toksoy G., Atay Z., Uyguner Z. O., Baş F., et al.
19. PEDİATRİK ENDOKRİNOLOJİ VE DİYABET KONGRESİ, Antalya, Turkey, 22 - 24 October 2015, (Full Text)
2015
2015134. Idrar steroid profili
Güran T.
XIX. ULUSAL PEDIATRIK ENDOKRINOLOJI KONGRESI, İstanbul, Turkey, 20 - 22 October 2015, (Full Text)
2015
2015135. 5 Reduktaz tip 2 eksikligi tanisinda GC MS ile steroid olcumlerinde diagnostik oranlarin normatif datasinin olusturulmasi
Güran T., Taylor A., Hughes B. A., Oneill D., Cedric S., Arlt W.
XIX. Ulusal Pediatrik Endokrinoloji ve Diyabet Kongresi, İstanbul, Turkey, 20 - 22 October 2015, (Full Text)
2015
2015136. Factors Effecting Response to Growth HormoneTreatment in Children with Turner Syndrome
Baş S., Abalı S., Atay Z., Haliloğlu B., Gurbanov Z., Güran T., et al.
54th Annual Meeting of the European Society for Paediatric Endocrinology (ESPE), Barcelona, Spain, 1 - 03 October 2015, (Summary Text)
2015
2015137. Hereditary Vitamin D Resistant Rickets Report of Four Cases with Successful Use of Intermittent Intravenous Calcium Via Peripheral Route
Abalı S., Tamura M., Atay Z., İşgüven Ş. P., Güran T., Haliloğlu T., et al.
54th Annual Meeting of the European Society for Paediatric Endocrinology (ESPE), Barcelona, Spain, 1 - 03 October 2015, (Summary Text)
2015
2015138. Aetiological Spectrum and Clinical Characteristics of 129 Children with Gonadotropin Independent Precocious Puberty A Nationwide Cohort Study
Atay Z., Yeşilkaya E., Erdeve Ş., Akın L., Eren E., Döger E., et al.
54th Annual Meeting of the European Society for Paediatric Endocrinology (ESPE), Barcelona, Spain, 1 - 03 October 2015, (Summary Text)
2015
2015139. Primary Adrenal Insufficiency in Children without Congenital Adrenal Hyperplasia Molecular and Clinical Characterisation of a Nationwide Cohort
Güran T., Buonocore F., Saka N., Özbek M. N., Aycan Z., Bereket A., et al.
54th Annual Meeting of the European Society for Paediatric Endocrinology (ESPE), Barcelona, Spain, 1 - 03 October 2015, (Full Text)
2015
2015140. Evaluating First Year Response and Final Height toGrowth Hormone Treatment in Growth HormoneDeficiency Based on Peak GH Levels on Testing
Abalı S., Baş S., Akbarzade A., Atay Z., Haliloğlu B., Güran T., et al.
54th Annual Meeting of the European Society for Paediatric Endocrinology (ESPE), Barcelona, Spain, 1 - 03 October 2015, (Summary Text)
2015
2015141. A novel mutation cdel209 in the proopiomelanocortin gene in a child with early onset obesity
CETINKAYA S., GÜRAN T., ERDAL K., Keskin M., Sagsak E., Savas Erdeve S., et al.
54th ESPE (European Society of Pediatric Endocrinology) meeting, Barselona, Spain, 29 September - 04 October 2015, vol.84, pp.1-622, (Full Text)
2015
2015142. Identification and functional characterization of ESR2 a new disease gene for 46 XY disorders of sex development DSD
Baetens D., Güran T., De Cauwer L., Looijenga L., De Bosscher K., Cools M., et al.
5th I-DSD Symposium, Ghent, Belgium, 11 - 13 June 2015, vol.84, (Full Text)
2015
2015143. Pubertal Development in Individuals with Partial Androgen Insensitivity Syndrome PAIS Assigned Female Sex of Rearing
Guaragnafilho G., Junior G. G., Darendeliler F., Balsamo A., Holterhus P., Güran T., et al.
5th I-DSD Symposium, Ghent, Belgium, 11 - 13 June 2015, vol.84, (Full Text)
2015
2015144. PROOPİOMELANOKORTİN POMC GENİNDE YENİ MUTASYONLU ERKEN BAŞLANGIÇLI BİR OBEZİTE OLGUSU
Cetınkaya S., Aycan Z., Güran T., Kurnaz E., Keskin M., Sağsak E., et al.
Ulusal Cocuk Endokrinoloji Dernegi 7. Olgu sunumlari toplantisi, İzmir, Turkey, 18 - 20 May 2015, (Full Text)
2015
2015145. ANTLEY BİXLER SENDROMLU BİR OLGUMUZ
Turan S., Bas S., Akay Tayfun G., Abalı S., Atay Z., Qurbanov Z., et al.
Cocuk Endokrinoloji Dernegi 7.Olgu Sunumlari Toplantisi, İzmir, Turkey, 18 - 20 May 2015, (Full Text)
2015
2015146. Urinary steroid Profiling
Güran T.
Disorders of Sex Development (DSD)- the roles of genes and the environment’PhD course, Soro, Denmark, 26 April - 27 October 2015, (Full Text)
2014
2014147. CHRONIC MUCOCUTANEOUS CANDIDIASIS, AUTOIMMUNE THYROIDITIS AND CEREBRAL MYCOTIC ANEURISM; STAT1 MUTATION
Kiykim A., Aydiner E., Ozen A. O., Baris S., Guran T., Hsu P. A., et al.
100th J Project Meeting, Antalya, Turkey, 12 - 14 March 2014, vol.34, pp.745, (Summary Text)
2014
2014148. Hipoglisemi: Kistik Fibrozise bağlı diyabet tanısında CGMS (sürekli glukoz izleme sistemi) ile OGTT nin karşılaştırılması
Haliloğlu B., Gökdemir Y., Atay Z., Abalı S., Güran T., Karakoç F., et al.
TTD 17. yıllık kongresi, Antalya, Turkey, 2 - 06 April 2014, (Full Text)
2011
2011149. Yenidoğanda hipogliseminin nadir bir nedeni: SUR 1 gen mutasyonuna bağlı hiperinsülinizm
MEMİŞOĞLU A., GÜRAN T., İNAN E., DEMİREL B., KARATEKİN G.
19. Ulusal Neonatoloji Kongresi, Turkey, 17 - 20 April 2011, (Summary Text)
2007
2007150. Identification of novel dentin matrix protein-1 (DMP1) mutations in two unrelated kindreds with autosomal recessive hypophosphatemia
Turan S., Bastepe M., Bereket A., Akcay T., Guran T., Makitie O., et al.
29th Annual Meeting of the American-Society-for-Bone-and-Mineral-Research, Hawaii, United States Of America, 16 - 19 September 2007, vol.22, (Summary Text)
2006
2006151. Sağlıklı bebeklerde serum alkalen fosfataz değerleri
Topçu B., Turan S., Gökce İ., Akçay T., Güran T., Bereket A.
11. Ulusal Pediatrik Endokrinoloji ve Diyabet Kongresi, Konya, Turkey, 14 - 17 September 2006, pp.118, (Summary Text)
Books
2022
20221. DSD and Gender Incongruence
Güran T.
in: ESPE Yearbook of Paediatric Endocrinology 2022 , Ken Ong,Christa Flück, Editor, Blackwell, Oxford , Bristol, pp.61-72, 2022
2022
20222. Congenital adrenal hyperplasia and hypertension
Güran T.
in: Endocrine Hypertension From Basic Science to Clinical Practice, Joseph M. Pappachan,Cornelius J. Fernandez, Editor, Elsevier Science, Oxford/Amsterdam , Oxford, pp.114-122, 2022
2021
20213. Prenatal diagnosis and treatment in Congenital adrenal hyperplasia
Yavas Abali Z., Güran T.
in: Fertility and reproductive outcomes indifferent forms of congenital adrenal hyperplasia, M.Eda Ertorer, Editor, Springer, London/Berlin , Basel, pp.127-141, 2021
2021
20214. Çocuklarda Adrenal Hastalıkların Uzaktan Yönetimi
Güran T.
in: Çocuk Endokrinolojisinde Teletıp - 2021, Prof. Dr. İlknur ARSLANOĞLU, Editor, Türkiye Klinikleri Yayınevi, Ankara, pp.30-36, 2021
2021
20215. Adrenal yetmezlik
Yavas Abali Z., Güran T.
in: Cocuk Endokrinolojisi ve Diyabet, Feyza Darendeliler,Zehra Aycan,Cengiz Kara,Samim Ozen,Erdal Eren, Editor, Istanbul Tip kitabevi, İstanbul, pp.965-990, 2021
2021
20216. Yenidoganda konjenital adrenal hiperplazi taramalari
Güran T.
in: Cocuk Endokrinolojisi ve Diyabet, Feyza Darendeliler,Zehra Aycan,Cengiz Kara,Samim Ozen,Erdal Eren, Editor, Istanbul Tip kitabevi, İstanbul, pp.112-118, 2021
2021
20217. Hormon analizlerinde temel laboratuar teknikleri ve cocuk endokrinoloji pratiginde kullanimi
Güran T., Yaman A., Bereket A.
in: Cocuk Endokrinolojisi ve Diyabet, Feyza Darendeliler,Zehra Aycan,Cengiz Kara,Samim Ozen,Erdal Eren, Editor, Istanbul Tip kitabevi, İstanbul, pp.96-112, 2021
2019
20198. Cocuklarda Cushing Sendromu
Güran T.
in: Butuncul Tip (Birinci Basamakta ve Aile Hekimliginde Guncel Tani-Tedavi), Doc Dr Aydin Cifci,Prof Dr Adem Ozkara,Dr Ogr Uyesi Serkan Tursun,Uzm Dr Bulut Demirel,Prof Dr Murat Kekilli, Editor, Nobel Tip Kitapevleri Ltd Sti, Ankara, pp.2118-2119, 2019
2019
20199. Cocuklarda adrenal bez hastaliklari
Güran T.
in: Butuncul Tip (Birinci Basamakta ve Aile Hekimliginde Guncel Tani-Tedavi), Doc Dr Aydin Cifci,Prof Dr Adem Ozkara,Dr Ogr Uyesi Serkan Tursun,Uzm Dr Bulut Demirel,Prof Dr Murat Kekilli., Editor, Nobel Tip Kitapevleri Ltd Sti, Ankara, pp.2106-2114, 2019
2019
201910. Cocuklarda endokrin hipertansiyon
Güran T.
in: Butuncul Tip (Birinci Basamakta ve Aile Hekimliginde Guncel Tani-Tedavi), Doc Dr Aydin Cifci,Prof Dr Adem Ozkara,Dr Ogr Uyesi Serkan Tursun,Uzm Dr Bulut Demirel,Prof Dr Murat Kekilli, Editor, Nobel Tip Kitapevleri Ltd Sti, Ankara, pp.2115-2117, 2019
2018
201811. Cinsiyet gelisim bozukluklari
Güran T.
in: Yogun Bakim Hemsireligi: Esaslar ve Uygulamalar , Prof Dr Eren Ozek- Prof Dr Hulya Selva Bilgen, Editor, Gunes Tip Kitabevleri, İstanbul, pp.393-403, 2018
2017
201712. Adrenal hastaliklar
Güran T.
in: Yurdakok Pediatri, Murat Yurdakok, Editor, Gunes Tip Kitapevleri, İstanbul, pp.4142-4154, 2017
2017
201713. ENDOKRİN SİSTEM HASTALIKLARI
Özcabı B., Dursun F., Güran T.
in: DİŞ HEKİMLİĞİ BAKIŞ AÇISIYLA SİSTEMİK HASTALIKLAR, ESRA BİHTER GÜRLER, Editor, QUINTESSENCE YAYINCILIK TANITIM PAZ. VE DIŞ.TİC.LTD.ŞTI, İstanbul, pp.19-37, 2017
2016
201614. The hypothalamo-pituitary-adrenal axis and its regulation
Baronowski L., Güran T., Krone N.
in: Neuroendocrine Disorders in Children , Mehul T Dattani,Peter C. Hindmarsh,Lucinda Carr and Iain C.A.F. Robinson., Editor, Mac Keith Press, London, pp.206-218, 2016
2014
201415. Yenidogan KAH taramalari, prenatal tani ve tedavi
Güran T., Ozsu E.
in: Cocuk Endokrinolojisinde Uzlasi, NA, Editor, Nobel Yayincilik., İstanbul, pp.103-106, 2014
2014
201416. Cinsiyet Gelisim Bozuklugu
Güran T.
in: Cocuk Endokrinolojisinde Uzlasi, NA, Editor, Nobel Yayincilik, İstanbul, pp.75-98, 2014
2013
201317. HORMON ÖLÇÜMÜNDE TEMEL LABORATUVAR TEKNİKLER VE ÇOCUK ENDOKRİNOLOJİ PRATİĞİNDE KULLANIMI
Bereket A., Güran T.
in: Çocuk Endokrinoloji, Peyami Cinaz,Feyza Darendeliler,Ayşehan Akıncı,Ayhan Abacı,Bumin Dündar,Teoman Akçay, Editor, Nobel Tıp Kitapevi, İstanbul, pp.7-18, 2013
2012
201218. Disorders of sexual development and genitourinary abnormalities
Bereket A., Güran T.
in: Moleküler Üroloji, Turkeri L,Ozer A,Narter F, Editor, Pelin Ofset Tipo Matbaacılık, Ankara, pp.623-653, 2012
2012
201219. Neuroendocrine control of reproductive system and related gene defects
Güran T., Bereket A.
in: Moleküler Üroloji, Turkeri L,Ozer A,Narter F, Editor, Pelin Ofset Tipo Matbaacılık, Ankara, pp.611-623, 2012
2010
201020. Pituitary hormones and hypopituitarism
Güran T., Bereket A.
in: Temel Pediatri (Türkiye Milli Pediatri Derneği), Hasanoglu E,Dusunsel R,Bideci A, Editor, Gunes Tip Kitabevleri, Ankara, pp.1119-1125, 2010
Funded Projects
2020 - 2021
2020 - 2021
An Observational, Prospective Natural History Study of Early-Onset Extreme Obesity Due to Bi-Allelic Loss-of-Function Mutations in the POMC, PCSK1 or LEPR Genes.
Project Supported by Private Organizations in Other Countries
Güran T. (Executive)
2017 - 2021
2017 - 2021A Phase 3 Randomized, Double-Blind, Placebo-Controlled, Parallel Group Study to Evaluate the Safety and Efficacy of Denosumab in Pediatric Subjects With Glucocorticoid-induced Osteoporosis
Project Supported by Private Organizations in Other Countries
Güran T., Turan S.(Executive)
Contractual Researches
2022 - 2023
2022 - 2023A Randomized, Double-Blind, Active-Controlled, Phase 3 Study of Chronocort Compared with Immediate-Release Hydrocortisone Replacement Therapy in Participants Aged 16 Years and Over with Congenital Adrenal Hyperplasia.
Diurnal
Güran T.
2022 - 2023
2022 - 2023Büyüme hormonu eksikliği olan ve daha önce büyüme hormonu tedavisi almamış prepubertal çocuklarda, haftada bir uygulanan NNC0195-0092 tedavisi ile, günlük uygulanan büyüme hormonu tedavisinin (Norditropin® FlexPro®) etkililik ve güvenlilik karşılaştırmasının araştırıldığı, randomize, çok uluslu, aktif kontrollü, (açık etiketli), doz bulma, (çift kör), paralel gruplu bir çalışma
NovoNordisk
Güran T., Demircioğlu S.
2018 - 2021
2018 - 2021A Phase 3 Randomized, Double-blind, Placebo-controlled, Parallel-group Study to Evaluate the Safety and Efficacy of Denosumab in Pediatric Subjects with Glucocorticoid-induced Osteoporosis (GiOP)
Amgen
Demircioğlu S. (Executive), Güran T., Buğdaycı O.
Activities in Scientific Journals
2021 - Continues
2021 - ContinuesHORMONE RESEARCH IN PAEDIATRICS
Assistant Editor/Section Editor
2021 - Continues
2021 - ContinuesHormone Research In Paediatrics
Special Issue Editor
2022 - 2022
2022 - 2022FRONTIERS IN GENETICS
Assistant Editor/Section Editor
2022 - 2022
2022 - 2022FRONTIERS IN GENETICS
Assistant Editor/Section Editor
Memberships and Roles in Scientific Organizations
2022 - Continues
2022 - ContinuesEuropean Society of Pediatric Endocrinology-Winter school Steering Committee
Board Member
2021 - Continues
2021 - Continues
Turk Cocuk Endokrinolojisi ve Diyabet Dernegi Adrenal Calisma Grubu
Vice President
2020 - Continues
2020 - Continues
Turk Cocuk Endokrinoloji ve Diyabet Dernegi
Secretary General
2020 - Continues
2020 - ContinuesI-DSD Steering Committee
Member
2019 - Continues
2019 - ContinuesEuropean society of pediatric endocrinology DSD working group
Chairman of the Scientific Committee
2018 - Continues
2018 - ContinuesEuropean Society of Pediatric Endocrinology Science Committee Expert Panel
Member of Science Committee
Peer Reviews in Scientific Publications
December 2022
December 2022IMPE-2023
Conference Paper (Full Text)
December 2022
December 2022endo-2023
Conference Paper (Full Text)
December 2022
December 2022PLOS ONE
Journal Indexed in SCI-E
November 2022
November 2022Endocrine Connections
Journal Indexed in SCI-E
November 2022
November 2022JOURNAL OF STEROID BIOCHEMISTRY AND MOLECULAR BIOLOGY
Journal Indexed in SCI-E
October 2022
October 2022PLOS ONE
Journal Indexed in SCI-E
October 2022
October 2022INTERNATIONAL JOURNAL OF ENDOCRINOLOGY
Journal Indexed in SCI-E
September 2022
September 2022FRONTIERS IN GENETICS
Journal Indexed in SCI-E
September 2022
September 2022JCRPE JOURNAL OF CLINICAL RESEARCH IN PEDIATRIC ENDOCRINOLOGY
Journal Indexed in SCI-E
September 2022
September 2022JOURNAL OF ENDOCRINOLOGICAL INVESTIGATION
Journal Indexed in SCI-E
September 2022
September 2022CLINICAL ENDOCRINOLOGY
Journal Indexed in SCI-E
September 2022
September 2022european society of Pediatric Endocrinology meeting-2022
Conference Paper (Full Text)
August 2022
August 2022HORMONE RESEARCH IN PAEDIATRICS
Journal Indexed in SCI-E
June 2022
June 2022HORMONE RESEARCH IN PAEDIATRICS
Journal Indexed in SCI-E
May 2022
May 2022FRONTIERS IN GENETICS
Journal Indexed in SCI-E
May 2022
May 2022JOURNAL OF CLINICAL ENDOCRINOLOGY AND METABOLISM
Journal Indexed in SCI-E
May 2022
May 2022JCRPE JOURNAL OF CLINICAL RESEARCH IN PEDIATRIC ENDOCRINOLOGY
Journal Indexed in SCI-E
April 2022
April 2022JOURNAL OF CLINICAL ENDOCRINOLOGY AND METABOLISM
Journal Indexed in SCI-E
April 2022
April 2022PLOS ONE
Journal Indexed in SCI-E
April 2022
April 2022upek-2022
Conference Paper (Full Text)
April 2022
April 2022EXPERIMENTAL AND CLINICAL ENDOCRINOLOGY AND DIABETES
Journal Indexed in SCI-E
February 2022
February 2022REVIEWS IN ENDOCRINE AND METABOLIC DISORDERS
Journal Indexed in SCI-E
February 2022
February 2022JOURNAL OF PEDIATRIC ENDOCRINOLOGY AND METABOLISM
Journal Indexed in SCI-E
January 2022
January 2022FRONTIERS IN ENDOCRINOLOGY
Journal Indexed in SCI-E
January 2022
January 2022JOURNAL OF STEROID BIOCHEMISTRY AND MOLECULAR BIOLOGY
Journal Indexed in SCI-E
October 2021
October 2021JOURNAL OF PEDIATRICS
Journal Indexed in SCI-E
September 2021
September 2021JOURNAL OF CLINICAL RESEARCH IN PEDIATRIC ENDOCRINOLOGY
Journal Indexed in SCI-E
July 2021
July 2021EUROPEAN JOURNAL OF ENDOCRINOLOGY
Journal Indexed in SCI-E
March 2021
March 2021JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM
Journal Indexed in SCI-E
February 2021
February 2021JOURNAL OF CLINICAL RESEARCH IN PEDIATRIC ENDOCRINOLOGY
Journal Indexed in SCI-E
Scientific Project Refereeing
May 2021
May 2021Other International Funding Programs
European Society of Pediatric Endocrinology Researchh Felowship, United Kingdom
May 2021
May 2021Other International Funding Programs
European Society of Pediatric Endocrinology Refearch fellowship, United Kingdom
Scientific Consultations
2022 - Continues
2022 - ContinuesProject Consultancy
büyüsün.org (https://buyusun.org/uzman-gorusleri/hasta-buyume-hormonu-tedavisi-almayi-reddederse-ne-yapmali/)
Marmara University, School of Medicine, Internal Medical Sciences, Turkey
2017 - Continues
2017 - ContinuesScientific Consultancy
Saglik bakanligi
Marmara University, School of Medicine, Internal Medical Sciences, Turkey
2022 - 2022
2022 - 2022Project Consultancy
marmara student congress
Marmara University, School of Medicine, Internal Medical Sciences, Turkey
Roles in Event Organizations
Ekim 2022
Ekim 2022XXVI. Ulusal Pediatrik Endokrinoloji ve Diyabet Kongresi
Scientific Congress
Demircioğlu S., GÜRAN T.
Turkey
Eylül 2022
Eylül 2022VIII. PEDİATRİK ENDOKRİNOLOJİYE GİRİŞ KURSU
Scientific Congress
Güran T.
Antalya, Turkey
Nisan 2022
Nisan 2022Steroids, Mass Spectrometry and Endocrinology – Past, Present and Future
Scientific Congress
Güran T.
Birmingham, England
Şubat 2022
Şubat 2022VII. PEDIATRIK ENDOKRINOLOJI ILERI KURSU
Scientific Congress
Güran T.
İstanbul, Turkey
Awards
September 2021
September 2021
People`s choice poster award
European Society Of Pediatric Endocrinology
November 2020
November 2020Kısa Sözel Bildiri Üçüncülük Ödülü- Biallelik PPP2R3C mutasyonları 46, XX ve 46, XY gonadal disgeneziye yol açar
Xxıv. Ulusal Pediatrik Endokrinoloji Ve Diyabet Çevrim İçi Kongresi
November 2020
November 2020Sözlu Bildiri Birincilik Ödülü Steroid 11β-hidroksilaz eksikliği olan 100 çocuk hastanın klinik bulgularının genetik ve adrenokortikal hormon profili ile ilişkisinin değerlendirilmesi
Xxıv. Ulusal Pediatrik Endokrinoloji Ve Diyabet Çevrim İçi Kongresi
November 2020
November 2020Poster Bildiri Birincilik Ödülü-Parsiyel Pankreatik Agenezi ve Sendromik Hipopituarizm
Xxıv. Ulusal Pediatrik Endokrinoloji Ve Diyabet Çevrim İçi Kongresi
October 2013
October 2013Best second oral presentation
Ulusal Pediatrik Endokrinoloji Kongresi Bilimsel Kurul
Congress and Symposium Activities
29 November 2022 - 29 November 2022
29 November 2022 - 29 November 2022NovoCME Continuous Medical Education International Academy online
Moderator
İstanbul-Turkey
08 November 2022 - 08 November 2022
08 November 2022 - 08 November 2022ÇEDD Uzaktan Eğitim Seminerleri
Moderator
İstanbul-Turkey
26 September 2022 - 30 September 2022
26 September 2022 - 30 September 2022
XXVI.ULUSAL PEDİATRİK ENDOKRİNOLOJİ VE DİYABET KONGRESİ
Invited Speaker
Antalya-Turkey
26 September 2022 - 30 September 2022
26 September 2022 - 30 September 2022
XXVI. Ulusal Pediatrik Endokrinoloji ve Diyabet Kongresi
Moderator
Antalya-Turkey
22 September 2022 - 24 September 2022
22 September 2022 - 24 September 20222. Cerrahpaşa Pediatri Günleri
Session Moderator
İstanbul-Turkey
15 September 2022 - 16 September 2022
15 September 2022 - 16 September 2022The European Society for Paediatric Endocrinology (ESPE) meeting 2022
Session Moderator
Rome-Italy
15 September 2022 - 17 September 2022
15 September 2022 - 17 September 2022European Society for Paediatric Endocrinology 2022 meeting
Moderator
Rome-Italy
15 September 2022 - 17 September 2022
15 September 2022 - 17 September 2022The European Society for Paediatric Endocrinology
Session Moderator
Rome-Italy
24 May 2022 - 24 May 2022
24 May 2022 - 24 May 2022NovoCME Continuous Medical Education International Academy online
Moderator
İstanbul-Turkey
13 May 2022 - 15 May 2022
13 May 2022 - 15 May 2022ÇOCUK ENDOKRİNOLOJİSİ OLGU SUNUMLARI -11
Session Moderator
İstanbul-Turkey
13 March 2022 - 16 March 2022
13 March 2022 - 16 March 202218. uLUDAG PEDIATRI kIS kONGRESI
Session Moderator
Bursa-Turkey
18 February 2022 - 20 February 2022
18 February 2022 - 20 February 20229. Marmara Pediatri Kongresi
Session Moderator
İstanbul-Turkey
09 November 2021 - 09 November 2021
09 November 2021 - 09 November 2021NovoCME Continuous Medical Education International Academy online
Moderator
İstanbul-Turkey
06 October 2021 - 10 October 2021
06 October 2021 - 10 October 2021
XXV. Ulusal Pediatrik Endokrinoloji ve Diyabet Kongresi
Session Moderator
Antalya-Turkey
22 September 2021 - 26 September 2021
22 September 2021 - 26 September 2021European Society for Paediatric Endocrinology 2021 meeting
Moderator
Liverpool-United Kingdom
08 July 2021 - 09 July 2021
08 July 2021 - 09 July 20218th I-DSD Symposium 2021
Session Moderator
Glasgow-United Kingdom
09 April 2021 - 10 April 2021
09 April 2021 - 10 April 202110.Olgu Sunumları Sempozyumu
Session Moderator
İzmir-Turkey
Invited Talks
October 2022
October 2022Ulusal yenidogan KAH taramasi
Conference
66. Türkiye Milli Pediatri Kongresi-Turkey
October 2022
October 2022Endokrin Hastalıkların Genetiği Seminerleri- 46,XY Primer Gonadal Yetmezlikte yeni bir gen: INHA
Seminar
ÇOCUK ENDOKRİNOLOJİSİ VE DİYABET DERNEĞİ-Turkey
September 2022
September 2022Cinsiyet Gelişim Bozukluğu Olgularında Endokrin Testlerin Yorumlanması - Tülay Güran (https://www.cocukendokrindiyabet.org/eogrenmeliste)
Seminar
ÇOCUK ENDOKRİNOLOJİSİ VE DİYABET DERNEĞİ-Turkey
September 2022
September 2022yearbook
Conference
The European Society for Paediatric Endocrinology-Italy
July 2022
July 2022Interpretation of endocrine tests
Conference
9th I-DSD Symposium 2022-Switzerland
July 2022
July 2022ESPE DSD working group
Conference
9th I-DSD Symposium 2022-Turkey
May 2022
May 2022Ulusal KAH taramasi
Conference
57. Türk Pediatri Kongresi - Kongre Uzmanı-Turkey
April 2022
April 2022Steroids, Mass Spectrometry and Endocrinology – Past, Present and Future
Conference
University of Birmingham-England
March 2022
March 2022Ulusal yenidogan KAH taramasi
Conference
Bursa Uludağ Üniversitesi-Turkey
February 2022
February 2022KAH Olgu Calismasi
Seminar
VII. Pediatrik Endokrinoloji İleri Kursu (PEİK)-Turkey
January 2022
January 2022Yenidoğan KAH Taraması Toplantısı: Sorunlar - Çözüm Önerileri - Tülay Güran(https://www.cocukendokrindiyabet.org/eogrenmeliste)
Seminar
ÇOCUK ENDOKRİNOLOJİSİ VE DİYABET DERNEĞİ-Turkey
November 2021
November 2021Türkiye`de Konjenital Adrenal Hiperplazi Yenidoğan Taraması: Verilerin Değerlendirilmesi
Conference
65. Türkiye Milli Pediatri Kongresi-Turkey
October 2021
October 2021Optimizing Medical Therapy in Different Forms of Congenital Adrenal Hyperplasia
Seminar
KONIKA XVIII Medan 2021-Indonesia
October 2021
October 202146,XX cinsiyet gelisim bozukluklarina yaklasim
Seminar
XXV. Ulusal Pediatrik Endokrinoloji ve Diyabet Kongresi-Turkey
October 2021
October 2021Common and rare adrenal causes of DSD
Seminar
BSPED DSD SIG Programme -United Kingdom
October 2021
October 2021Steroidogenezde Aberan Androjen Üretimi ve Klinik Yansımaları
Seminar
XXV. Ulusal Pediatrik Endokrinoloji ve Diyabet Kongresi-Turkey
June 2021
June 2021KONJENİTAL ADRENAL HİPERPLAZİNİN YÖNETİMİ
Seminar
VI. Pediatrik Endokrinoloji İleri Kursu-Turkey
May 2021
May 2021Optimizing Medical Therapy in Different Forms of Congenital Adrenal Hyperplasia
Seminar
Indian Society for Pediatric and Adolescent Endocrinology (ISPAE)Academics and Clinical Education Series (ISPAE - ACES)-India
April 2021
April 2021Cocuklarda gecikmis ergenlik
Seminar
Endokrinoloji Talim-Turkey
March 2021
March 2021Steroidogenezde Arka Yolak Hastalıklarının Klinik Yansımaları
Seminar
4. Ege Endokrin Hastalıklar ve Genetik Sempozyumu-Turkey
January 2021
January 2021Konjenital Adrenal Hiperplazi Tanısında Zorluklar
Seminar
Endokrin Hastalıkların Genetiği Seminerleri-Turkey
November 2020
November 202046, XX Cinsiyet gelişim bozukluklarına yaklaşım
Seminar
VI. PEDİATRİK ENDOKRİNOLOJİYE GİRİŞ KURSU -Turkey
October 2020
October 2020Geç tanı alan Turner sendromu olgusunda büyüme hormonu tedavisi ve puberte induksiyonu
Seminar
NordiPEVA Büyüyen Tecrübe Toplantısı-Turkey
September 2020
September 2020Adrenal Yetmezlik ve Yönetimi
Seminar
Çocuk Endokrinolojisinde Güncellemeler-Turkey
April 2020
April 2020Endokrin Söyleşiler-Yeni Gen Keşfinde Yolculuk
Seminar
24. Ulusal Pediatrik Endokrinoloji ve Diyabet Kongresi-Turkey
Scholarships
2022 - 2023
2022 - 2023Desteklenen Araştırma Ödülleri (Yurtiçi)
Other Government Agencies
2022 - 2022
2022 - 2022BAPKO TTU-2022-10603
University
2022 - 2022
2022 - 2022Desteklenen Araştırma Ödülleri (Yurtiçi)
Other Government Agencies
2021 - 2021
2021 - 2021Registration Grant
Other International Organizations
2021 - 2021
2021 - 2021Registration grant
Other International Organizations
2021 - 2021
2021 - 2021Registration grant
Other International Organizations
Citations
Total Citations (WOS): 2710
h-index (WOS): 26
Jury Memberships
December-2022
December 2022Appointment to Academic Staff-Assistant Professorship
UZM. DR. ASLI DERYA KARDELEN AL -DOKTOR ÖĞRETİM ÜYESİ KADROSUNA ATAMA - Marmara Üniversitesi
November-2022
November 2022Doctoral Examination
Ceren Alavanda-uzmanlik sinavi - Marmara Üniversitesi
October-2022
October 2022Expertise In Medicine
Ceren Alavanda-tez sinavi - Marmara Üniversitesi
September-2022
September 2022Doctoral Examination
Hazal Gecamer-uzmanlik sinavi - Marmara Üniversitesi
September-2022
September 2022Appointment to Academic Staff-Assistant Professorship
Fatma Dursun-Docentlik Kadrosuna Atanma - Sağlık Bilimleri Üniversitesi
August-2022
August 2022Expertise In Medicine
Hazal Gecamer-tez sinavi - Marmara Üniversitesi
July-2022
July 2022Associate Professor Exam
Doçentlik Sınav Jürisi, Üniversitelerarası Kurul-Melike Demiral - Marmara University
May-2022
May 2022Award
marmara student congress - Marmara Üniversitesi
May-2022
May 2022Appointment to Academic Staff-Professorship
Gonul Catli-Profesor Kadrosuna Atanma - Altınbaş Üniversitesi
May-2022
May 2022Award
european society of pediatric endocrinology research unit board member - Marmara University
April-2022
April 2022Expertise In Medicine
Busra Gurpinar Tosun- Uzmanlik sinavi - Marmara Üniversitesi
March-2022
March 2022Associate Professor Exam
Doçentlik Sınav Jürisi, Üniversitelerarası Kurul-Selin Elmaogullari - Marmara University
November-2021
November 2021Expertise In Medicine
Dr Tuba Seven Menevse Yan dal uzmanlik - Marmara Üniversitesi
August-2021
August 2021Appointment to Academic Staff-Professorship
Doc Dr R. Gul Yesiltepe Mutlu nun profesorluk kadrosuna atanmasi - Koç Üniversitesi
July-2021
July 2021Expertise In Medicine
Dr Sare Betul Kaygusuz yandal uzmanlik - Marmara Üniversitesi
May-2021
May 2021Associate Professor Exam
Dr Erdal Kurnaz in docentlik jurisi - Sağlık Bilimleri Üniversitesi
April-2021
April 2021Expertise In Medicine
Dr Mehmet EltanYandal uzmanlik - Marmara Üniversitesi
March-2021
March 2021Appointment to Academic Staff-Assistant Professorship
Doc Dr Heves Kirmizi pekmezin akademik kadroya atanmasi - Sağlık Bilimleri Üniversitesi
February-2021
February 2021Appointment to Academic Staff-Professorship
Doc Dr Atilla Cayir in profesorluk kadrosuna atanmasi - Sağlık Bilimleri Üniversitesi
February-2021
February 2021Appointment to Academic Staff-Professorship
Doc Dr Rabia Gonul Yamanel profesorluk kadrosuna atanmasi - Sağlık Bilimleri Üniversitesi
March-2020
March 2020Appointment to Academic Staff-Assistant Professorship
Doc Dr Bulent Hacihamdioglu nun akademik akdroya atanmasi - İstanbul Aydın Üniversitesi
March-2020
March 2020Associate Professor Exam
Dr Hale Unver Tuhan docentlik basvurusu - Marmara Üniversitesi
December-2019
December 2019Appointment to Academic Staff-Professorship
Prof Dr Cengiz KARA nin akademik kadroya atanmasi - Altınbaş Üniversitesi
March-2019
March 2019Associate Professor Exam
Dr Ozlem Korkmaz docentlik basvurusu - Marmara Üniversitesi
November-2018
November 2018Appointment to Academic Staff-Professorship
Doc Dr Zeynep Seda Uyan in profesorluk kadrosuna atanmasi - Koç Üniversitesi
December-2017
December 2017Associate Professor Exam
Dr Belma Haliloglu nun docentlik basvurusu - Marmara Üniversitesi
October-2017
October 2017