Prof.

TÜLAY GÜRAN


School of Medicine

Internal Medical Sciences

Department of Pediatrics

Education Information

2004 - 2009

2004 - 2009

Post Doctorate of Medicine

Marmara University, School of Medicine, Internal Medical Sciences, Turkey

1999 - 2004

1999 - 2004

Expertise In Medicine

Marmara University, School of Medicine, Internal Medical Sciences, Turkey

1992 - 1999

1992 - 1999

Undergraduate

İstanbul Üniversitesi, Cerrahpaşa Tıp Fakültesi, Cerrahpaşa Tıp Pr. (İngilizce), Turkey

Research Areas

Health Sciences

Academic Titles / Tasks

2017 - Continues

2017 - Continues

Professor

Marmara University, School Of Medicine, Internal Medical Sciences

Articles Published in Journals That Entered SCI, SSCI and AHCI Indexes

2021

2021

mTOR-Activating Mutations in <i>RRAGD</i> Are Causative for Kidney Tubulopathy and Cardiomyopathy.

Schlingmann K. P. , Jouret F., Shen K., Nigam A., Arjona F. J. , Dafinger C., et al.

Journal of the American Society of Nephrology : JASN, vol.32, no.11, pp.2885-2899, 2021 (Journal Indexed in SCI Expanded) identifier

2021

2021

Introduction.

Guran T. , Flück C. E.

Hormone research in paediatrics, 2021 (Journal Indexed in SCI Expanded) identifier

2021

2021

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 (Journal Indexed in SCI Expanded) identifier identifier identifier

2021

2021

Machine Learning Quest for Predictive Markers of Lifestyle Modification Outcomes in Pediatric Obesity Treatment

Gawlik A., Shmoish M., BEREKET A. , Wasniewska M., Antosz A., Kirkgoz T., et al.

HORMONE RESEARCH IN PAEDIATRICS, vol.94, no.SUPPL 1, pp.275, 2021 (Journal Indexed in SCI) Sustainable Development identifier

2021

2021

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 (Journal Indexed in SCI) identifier

2021

2021

Coexistence of Adrenal Insufficiency and Hypergonadotropic Hypogonadism: P450scc Deficiency

Sakar M., Erdeve S. S. , Güran T. , Aycan Z., Cetinkaya S.

HORMONE RESEARCH IN PAEDIATRICS, vol.94, no.SUPPL 1, pp.203, 2021 (Journal Indexed in SCI) identifier

2021

2021

Hyperinsulinemic hypoglycemia due to biallelic mutations in the DNAJC3 gene

Gürpınar Tosun B. , Seven Menevşe T. , Esen N., Demircioğlu S. , Yesilyurt A., Güran T. , et al.

HORMONE RESEARCH IN PAEDIATRICS, vol.94, no.SUPPL 1, pp.107, 2021 (Journal Indexed in SCI) identifier

2021

2021

46,XY DSD due to biallelic DHX37 gene mutations

Eltan M. , Helvacioglu D., Ates E. A. , Abali Z. Y. , Demircioğlu S. , Bereket A. , et al.

HORMONE RESEARCH IN PAEDIATRICS, vol.94, no.SUPPL 1, pp.393-394, 2021 (Journal Indexed in SCI) identifier

2021

2021

Biallelic PPP2R3C mutations are associated with partial and complete gonadal dysgenesis in 46,XY and 46,XX individuals

Çiçek D., Warr N., Yesil G., Eker H. K. , Bas F., Poyrazoglu S., et al.

HORMONE RESEARCH IN PAEDIATRICS, vol.94, no.SUPPL 1, pp.92, 2021 (Journal Indexed in SCI) identifier

2021

2021

Rahman Syndrome: Hypopituitarism might be responsible for changing height pattern

Kaygusuz S. B. , Demircioğlu S. , Esen N., Bereket A. , Yesilyurt A., Güran T.

HORMONE RESEARCH IN PAEDIATRICS, vol.94, no.SUPPL 1, pp.359, 2021 (Journal Indexed in SCI) identifier

2021

2021

Broad range of phenotypes in an international cohort of 75 DSD individuals with SF-1/NR5A1 variants

Kouri C., Sommer G., Ahmed F., Balsamo A., Baronio F., Bryce J., et al.

HORMONE RESEARCH IN PAEDIATRICS, vol.94, no.SUPPL 1, pp.87-89, 2021 (Journal Indexed in SCI) identifier

2021

2021

Gonadal Outcome in 17beta-HSD deficiency and 5alpha-reductase deficiency

Boogers L. S. , Bruggenwirth H. T. , van Bever Y., Hersmus R., Bryce J., Ahmed S. F. , et al.

HORMONE RESEARCH IN PAEDIATRICS, vol.94, no.SUPPL 1, pp.91-92, 2021 (Journal Indexed in SCI) identifier

2021

2021

A rare cause of hypercalcemia: Congenital Lactase Deficiency

Eltan M. , Alavanda C. , Abalı S., Abali Z. Y. , Kaygusuz S. B. , Gürpınar Tosun B. , et al.

HORMONE RESEARCH IN PAEDIATRICS, vol.94, no.SUPPL 1, pp.75, 2021 (Journal Indexed in SCI) identifier

2021

2021

Clinical and Hormonal Profiles Correlate With Molecular Characteristics in Patients With 11β-Hydroxylase Deficiency.

Yildiz M., Isik E., Abali Z. Y. , Keskin M., Ozbek M. N. , Bas F., et al.

The Journal of clinical endocrinology and metabolism, vol.106, no.9, 2021 (Journal Indexed in SCI Expanded) identifier identifier identifier

2021

2021

Cranial MRI Abnormalities and Long-term Follow-up of the Lesions in 770 Girls With Central Precocious Puberty.

Helvacıoğlu D., Demircioğlu Turan S. , Güran T. , Atay Z., Dağçınar A., Bezen D., et al.

The Journal of clinical endocrinology and metabolism, vol.106, no.7, 2021 (Journal Indexed in SCI Expanded) identifier identifier identifier

2021

2021

Gonadectomy in conditions affecting sex development: a registry-based cohort study.

Lucas-Herald A. K. , Bryce J., Kyriakou A., Ljubicic M. L. , Arlt W., Audi L., et al.

European journal of endocrinology, vol.184, no.6, pp.791-801, 2021 (Journal Indexed in SCI Expanded) Creative Commons License identifier identifier

2021

2021

MANAGEMENT OF RAPIDLY PROGRESSIVE PRECOCIOUS PUBERTY IN A PATIENT WITH MOSAIC TURNER SYNDROME

Ozcabi B., Kirmizibekmez H., Mutlu G. Y. , Dursun F., Guran T.

ACTA ENDOCRINOLOGICA-BUCHAREST, vol.17, no.1, pp.101-105, 2021 (Journal Indexed in SCI) identifier identifier identifier

2020

2020

Neonatal Screening for Congenital Adrenal Hyperplasia in Turkey: Outcomes of Extended Pilot Study in 241,083 Infants

Güran T. , Tezel B., Cakir M., Akıncı A., Orbak Z., Keskin M., et al.

JOURNAL OF CLINICAL RESEARCH IN PEDIATRIC ENDOCRINOLOGY, vol.12, no.3, pp.287-294, 2020 (Journal Indexed in SCI) Sustainable Development identifier identifier identifier

2020

2020

Sphingosine-1-phosphate lyase (SGPL1) deficiency is associated with mitochondrial dysfunction

Maharaj A., Williams J., Bradshaw T., GÜRAN T. , Braslavsky D., Casas J., et al.

JOURNAL OF STEROID BIOCHEMISTRY AND MOLECULAR BIOLOGY, vol.202, 2020 (Journal Indexed in SCI) Sustainable Development identifier identifier identifier

2020

2020

Clinical Significance of Hypophosphatasemia in Children

Bayramli R., Cevlik T., Güran T. , Atay Z., Bas S., Haklar G. , et al.

CALCIFIED TISSUE INTERNATIONAL, vol.106, no.6, pp.608-615, 2020 (Journal Indexed in SCI) Sustainable Development identifier identifier identifier

2020

2020

Nationwide Turkish Cohort Study of Hypophosphatemic Rickets

Şıklar Z., Demircioğlu S. , Bereket A. , Bas F., Güran T. , Akberzade A., et al.

JOURNAL OF CLINICAL RESEARCH IN PEDIATRIC ENDOCRINOLOGY, vol.12, no.2, pp.150-159, 2020 (Journal Indexed in SCI) identifier identifier identifier

2020

2020

Revisiting Classical 3 beta-hydroxysteroid Dehydrogenase 2 Deficiency: Lessons from 31 Pediatric Cases

Güran T. , Kara C., Yildiz M., Bitkin E. C. , Haklar G. , Lin J., et al.

JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, vol.105, no.4, 2020 (Journal Indexed in SCI) identifier identifier identifier

2020

2020

Rare cause of severe hypertension in an adolescent boy presenting with short stature: Questions

Yavas A., Yesil G., Kirkgoz T., Cicek N., Alpay H. , Turan S. , et al.

PEDIATRIC NEPHROLOGY, vol.35, no.3, pp.403-404, 2020 (Journal Indexed in SCI) identifier identifier

2020

2020

Rare cause of severe hypertension in an adolescent boy presenting with short stature: Answers

Yavas A., Yesil G., Kirkgoz T., Cicek N., Alpay H. , Turan S. , et al.

PEDIATRIC NEPHROLOGY, vol.35, no.3, pp.405-407, 2020 (Journal Indexed in SCI) identifier identifier

2020

2020

A rare cause of chronic hyponatremia in an infant: Questions

Mutlu G. Y. , Tasdemir M., Kizilkan N. U. , Güran T. , Hatun S., Kayserili H., et al.

PEDIATRIC NEPHROLOGY, vol.35, no.2, pp.241-245, 2020 (Journal Indexed in SCI) identifier identifier

2020

2020

A rare cause of chronic hyponatremia in an infant: Answers

Mutlu G. Y. , Taşdemir M., Kızılkan N. U. , GÜRAN T. , Hatun Ş., Kayserili H., et al.

Pediatric Nephrology, vol.35, no.2, pp.243-245, 2020 (Journal Indexed in SCI Expanded) identifier identifier

2020

2020

A broad range of symptoms in allgrove syndrome: single center experience in Southeast Anatolia

Polat R., Ustyol A., Tuncez E., Guran T.

JOURNAL OF ENDOCRINOLOGICAL INVESTIGATION, vol.43, no.2, pp.185-196, 2020 (Journal Indexed in SCI) identifier identifier identifier

2020

2020

Restoration of Height after 11 Years of Letrozole Treatment in 11 beta-Hydroxylase Deficiency

Atay Z., Turan S. , Buǧdaycl O. , GÜRAN T. , BEREKET A.

HORMONE RESEARCH IN PAEDIATRICS, vol.92, no.3, pp.203-208, 2020 (Journal Indexed in SCI) identifier identifier identifier

2020

2020

Plasma Renin Measurements are Unrelated to Mineralocorticoid Replacement Dose in Patients With Primary Adrenal Insufficiency

Pofi R., Prete A., Thornton-Jones V., Bryce J., Ali S. R. , Ahmed S. F. , et al.

JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, vol.105, no.1, pp.314-326, 2020 (Journal Indexed in SCI) identifier identifier identifier

2020

2020

A rare cause of hypertension in childhood: Answers

Kucuk N., Yavas Abalı Z., ABALI S., Canpolat N., YEŞİL G., Turan S. , et al.

Pediatric Nephrology, vol.35, no.1, pp.79-82, 2020 (Journal Indexed in SCI) identifier identifier identifier

2020

2020

A rare cause of hypertension in childhood: Questions

Kucuk N., Yavas A., Abali S., Canpolat N., Yesil G., Turan S. , et al.

PEDIATRIC NEPHROLOGY, vol.35, no.1, pp.77-78, 2020 (Journal Indexed in SCI) identifier identifier identifier

2019

2019

Clinical but Not Histological Outcomes in Males With 45,X/46,XY Mosaicism Vary Depending on Reason for Diagnosis

Ljubicic M. L. , Jorgensen A., Acerini C., Andrade J., Balsamo A., Bertelloni S., et al.

JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, vol.104, no.10, pp.4366-4381, 2019 (Journal Indexed in SCI) Creative Commons License identifier identifier identifier

2019

2019

Evaluation of brain MRI lesions in 381 girls with central precocious puberty

Helvacioglu D., GÜRAN T. , KIRKGÖZ T. , Atay Z., Abali Z. Y. , ELTAN M. , et al.

HORMONE RESEARCH IN PAEDIATRICS, vol.91, pp.329-330, 2019 (Journal Indexed in SCI) identifier

2019

2019

Simplifying the interpretation of steroid metabolome data by a machine-learning approach

Kırkgöz T. , Kilic S., Abali Z. Y. , Yaman A., Kaygusuz S. B. , Eltan M. , et al.

HORMONE RESEARCH IN PAEDIATRICS, vol.91, pp.128, 2019 (Journal Indexed in SCI) identifier

2019

2019

A rare cause of 46, XX ovotesticular DSD: Tetragametic gonadal chimerism

Ucar A., GÜRAN T. , Eren F., Dokucu A. I. , Sahin S., Tanik C.

HORMONE RESEARCH IN PAEDIATRICS, vol.91, pp.480, 2019 (Journal Indexed in SCI) identifier

2019

2019

A 46, XX patient with 21-OHD diagnosed during the etiologic workup of male infertility

Bugrul F., Yildirak E., Güran T.

HORMONE RESEARCH IN PAEDIATRICS, vol.91, pp.502, 2019 (Journal Indexed in SCI) identifier

2019

2019

Contemporary surgical approach in CAH 46XX-Results from the I-DSD/I-CAH Registries

Hebenstreit D., Ahmed F., Springer A., Krall C., Krone N., Birkebaek N., et al.

HORMONE RESEARCH IN PAEDIATRICS, vol.91, pp.96-97, 2019 (Journal Indexed in SCI) identifier

2019

2019

A Case Of Syndromic Hypopituitarism

Kaygusuz S. B. , Ates E. A. , Kırkgöz T. , Eltan M. , Abali Z. Y. , Helvacioglu D., et al.

HORMONE RESEARCH IN PAEDIATRICS, vol.91, pp.589, 2019 (Journal Indexed in SCI) identifier

2019

2019

Rare Causes of Osteogenesis Imperfecta are Common in Consanguineous Pedigrees

Kaygusuz S. B. , Arman A. , Abalı S., Ata P. , Kırkgöz T. , Eltan M. , et al.

HORMONE RESEARCH IN PAEDIATRICS, vol.91, pp.214, 2019 (Journal Indexed in SCI) identifier

2019

2019

A rare cause of SRY (-) 46, XX DSD: Aromatase deficiency

Bugrul F., Güran T.

HORMONE RESEARCH IN PAEDIATRICS, vol.91, pp.597-598, 2019 (Journal Indexed in SCI) identifier

2019

2019

A rare cause of hypophosphatemia: Raine Syndrome

Eltan M. , Ata P. , Kırkgöz T. , Alavanda C. , Kaygusuz S. B. , Menevse T. S. , et al.

HORMONE RESEARCH IN PAEDIATRICS, vol.91, pp.384, 2019 (Journal Indexed in SCI) identifier

2019

2019

Exome Sequencing of a Primary Ovarian Insufficiency Cohort Reveals Common Molecular Etiologies for a Spectrum of Disease

Jolly A., Bayram Y., Turan S. , Aycan Z., Tos T., Abali Z. Y. , et al.

Journal of Clinical Endocrinology and Metabolism, vol.104, no.8, pp.3049-3067, 2019 (Journal Indexed in SCI) identifier identifier identifier

2019

2019

Evaluation of growth and puberty in a child with a novel TBX19 gene mutation and review of the literature

Abali Z. Y. , Yeşil G., Kırkgöz T. , Kaygusuz S. B. , Eltan M. , Turan S. , et al.

HORMONES-INTERNATIONAL JOURNAL OF ENDOCRINOLOGY AND METABOLISM, vol.18, no.2, pp.229-236, 2019 (Journal Indexed in SCI) identifier identifier identifier

2019

2019

Clinical and Laboratory Characteristics of Hyperprolactinemia in Children and Adolescents: National Survey

Eren E., Törel Ergür A., Pınar İşgüven Ş., Çelebi Bitkin E., Berberoğlu M., Şiklar Z., et al.

Journal of clinical research in pediatric endocrinology, vol.11, no.2, pp.149-156, 2019 (Journal Indexed in SCI Expanded) Sustainable Development identifier identifier identifier

2019

2019

PPP2R3C gene variants cause syndromic 46,XY gonadal dysgenesis and impaired spermatogenesis in humans

Güran T. , Yesil G., Turan S. , Atay Z., Bozkurtlar E. , Aghayev A., et al.

EUROPEAN JOURNAL OF ENDOCRINOLOGY, vol.180, no.5, pp.291-309, 2019 (Journal Indexed in SCI) identifier identifier identifier

2019

2019

Neonatal Screening for Congenital Adrenal Hyperplasia in Turkey: A Pilot Study with 38,935 Infants

Güran T. , Tezel B., Gürbüz F., Eklioğlu B. S. , Hatipoğlu N., Kara C., et al.

JOURNAL OF CLINICAL RESEARCH IN PEDIATRIC ENDOCRINOLOGY, vol.11, no.1, pp.13-23, 2019 (Journal Indexed in SCI) identifier identifier identifier

2018

2018

Incidence of Type 1 Diabetes in Children Aged Below 18 Years during 2013-2015 in Northwest Turkey

Poyrazoglu S., Bundak R., Abali Z. Y. , Onal H., Sarikaya S., Akgun A., et al.

JOURNAL OF CLINICAL RESEARCH IN PEDIATRIC ENDOCRINOLOGY, vol.10, no.4, pp.336-342, 2018 (Journal Indexed in SCI) Sustainable Development identifier identifier identifier

2018

2018

A RARE CAUSE OF CHRONIC HYPONATREMIA IN AN INFANT: ALDOSTERONE SYNTHASE TYPE-2 DEFICIENCY

Mutlu G. Y. , Tasdemir M., Kizilkan N. U. , Yucel E., GÜRAN T. , Hatun S., et al.

PEDIATRIC NEPHROLOGY, vol.33, no.10, pp.1971, 2018 (Journal Indexed in SCI) identifier

2018

2018

Primary adrenal insufficiency in children: Diagnosis and management

Kirkgoz T. , Fellow C., Güran T.

BEST PRACTICE & RESEARCH CLINICAL ENDOCRINOLOGY & METABOLISM, vol.32, no.4, pp.397-424, 2018 (Journal Indexed in SCI) Sustainable Development identifier identifier identifier

2018

2018

The Distribution of Different Types of Diabetes in Childhood: A Single Center Experience

Haliloğlu B. , ABALI S., Buğrul F., Çelik E., Baş S., Atay Z., et al.

Journal of clinical research in pediatric endocrinology, vol.10, no.2, pp.125-130, 2018 (Journal Indexed in SCI Expanded) Sustainable Development identifier identifier identifier

2018

2018

Mutations in the mitochondrial ribosomal protein MRPS22 lead to primary ovarian insufficiency

Chen A., Tiosano D., Guran T. , Baris H. N. , Bayram Y., Mory A., et al.

Human Molecular Genetics, vol.27, no.11, pp.1913-1926, 2018 (Journal Indexed in SCI) identifier identifier identifier

2018

2018

A Patient with Proopiomelanocortin Deficiency: An Increasingly Important Diagnosis to Make

Cetinkaya S., GÜRAN T. , Kurnaz E., Keskin M., Sagsak E., Erdeve S. S. , et al.

JOURNAL OF CLINICAL RESEARCH IN PEDIATRIC ENDOCRINOLOGY, vol.10, no.1, pp.68-73, 2018 (Journal Indexed in SCI) Sustainable Development identifier

2018

2018

Nationwide Hypophosphatemic Rickets Study

ŞIKLAR Z., Turan S. , BEREKET A. , ABACI A., Bas F., DEMİR K., et al.

HORMONE RESEARCH IN PAEDIATRICS, vol.90, pp.109-110, 2018 (Journal Indexed in SCI) identifier

2018

2018

Delayed Diagnosis of a Patient with Antley-Bixler Syndrome

Kırkgöz T. , Bas S., Abali Z. Y. , Turan S. , Bereket A. , Güran T.

HORMONE RESEARCH IN PAEDIATRICS, vol.90, pp.166-167, 2018 (Journal Indexed in SCI) identifier

2018

2018

Isolated Congenital Central Hypothyroidism due to a Novel Mutation in TSH Beta Subunit Gene

Kırkgöz T. , Özhan B., Cetin O., Kaygusuz S. B. , Turan S. , Bereket A. , et al.

HORMONE RESEARCH IN PAEDIATRICS, vol.90, pp.597, 2018 (Journal Indexed in SCI) identifier

2018

2018

An Unusual Cause of Short Stature

Kaygusuz S. B. , Atay Z., Kırkgöz T. , Güran T. , Bereket A. , Turan S.

HORMONE RESEARCH IN PAEDIATRICS, vol.90, pp.184-185, 2018 (Journal Indexed in SCI) identifier

2018

2018

Neonatal Screening for Congenital Adrenal Hyperplasia in Turkey: A Pilot Study with 38,935 Infants

Guran T. , Tezel B., Gurbuz F., Eklioglu B. S. , Hatipoğlu N., Kara C., et al.

HORMONE RESEARCH IN PAEDIATRICS, vol.90, pp.141-142, 2018 (Journal Indexed in SCI) identifier

2017

2017

Latest Insights on the Etiology and Management of Primary Adrenal Insufficiency in Children

GÜRAN T.

JOURNAL OF CLINICAL RESEARCH IN PEDIATRIC ENDOCRINOLOGY, vol.9, pp.9-22, 2017 (Journal Indexed in SCI) identifier identifier identifier

2017

2017

Genetic Disruption of 21-Hydroxylase in Zebrafish Causes Interrenal Hyperplasia

Eachus H., Zaucker A., Oakes J. A. , Griffin A., Weger M., Guran T. , et al.

ENDOCRINOLOGY, vol.158, no.12, pp.4165-4173, 2017 (Journal Indexed in SCI) Creative Commons License identifier identifier identifier

2017

2017

Hypoglycemia is common in children with cystic fibrosis and seen predominantly in females.

Haliloglu B. , Gökdemir Y. , Atay Z., Abali S., Güran T. , Karakoc F., et al.

Pediatric diabetes, vol.18, no.7, pp.607-613, 2017 (Journal Indexed in SCI Expanded) identifier identifier identifier

2017

2017

A RARE ENDOCRINE CAUSE OF HYPERTENSION: APPARENT MINERALOCORTICOID ACCESS SYNDROME

Kucuk N., Abali S., Canpolat N., Akin Y., Meric I., Esmi E., et al.

PEDIATRIC NEPHROLOGY, vol.32, no.9, pp.1744-1745, 2017 (Journal Indexed in SCI) identifier

2017

2017

Evaluation and Treatment Results of Ovarian Cysts in Childhood and Adolescence: A Multicenter, Retrospective Study of 100 Patients.

Aydin B. K. , Saka N., Bas F., Yilmaz Y., Haliloglu B. , GÜRAN T. , et al.

Journal of pediatric and adolescent gynecology, vol.30, no.4, pp.449-455, 2017 (Journal Indexed in SCI Expanded) identifier identifier identifier

2017

2017

Clinical, biochemical and genetic features with nonclassical 21-hydroxylase deficiency and final height

Savas-Erdeve S., Cetinkaya S., Abali Z. Y. , Poyrazoglu S., Bas F., BERBEROĞLU M., et al.

JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM, vol.30, no.7, pp.759-766, 2017 (Journal Indexed in SCI) identifier identifier identifier

2017

2017

Birth Weight in Different Etiologies of Disorders of Sex Development

Poyrazoglu S., Darendeliler F., Ahmed S. F. , Hughes I., Bryce J., Jiang J., et al.

JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, vol.102, no.3, pp.1044-1050, 2017 (Journal Indexed in SCI) identifier identifier identifier

2017

2017

17OH-PREGNENOLONE SEEMS A MAJOR DRIVE OF ANDROGEN EXCESS IN PATIENTS WITH 11 beta-HYDROXYLASE DEFICIENCY

Yildiz M., Turan S. , Akcay T., Atay Z., Onal H., Baris T., et al.

HORMONE RESEARCH IN PAEDIATRICS, vol.88, pp.54, 2017 (Journal Indexed in SCI) identifier

2017

2017

CYP11A1 MUTATIONS RESULT VARIOUS CLINICAL PHENOTYPES

Guven A., Buonocore F., Achermann J., GÜRAN T.

HORMONE RESEARCH IN PAEDIATRICS, vol.88, pp.73-74, 2017 (Journal Indexed in SCI) identifier

2017

2017

FAMILIAL GLUCOCORTICOID DEFICIENCY TYPE 2: A NEW MUTATION IN THE MRAP GENE P. K30DEL

BİDECİ A., DÖĞER E., Akbas E. D. , Ugurlu A. K. , GÜRAN T. , Camurdan O., et al.

HORMONE RESEARCH IN PAEDIATRICS, vol.88, pp.72, 2017 (Journal Indexed in SCI) identifier

2017

2017

17-HYDROXYLASE DEFICIENCY: RARE CAUSE OF DELAYED PUBERTY

Guven A., GÜRAN T. , Krone N.

HORMONE RESEARCH IN PAEDIATRICS, vol.88, pp.255-256, 2017 (Journal Indexed in SCI) identifier

2017

2017

ALDOSTERONE SYNTHASE DEFICIENCY : A NEW MUTATION

DÖĞER E., Ugurlu A. K. , Kazancioglu A., Akbas E. D. , GÜRAN T. , BİDECİ A., et al.

HORMONE RESEARCH IN PAEDIATRICS, vol.88, pp.73, 2017 (Journal Indexed in SCI) identifier

2016

2016

The Long-Term Outcome of Boys With Partial Androgen Insensitivity Syndrome and a Mutation in the Androgen Receptor Gene

Lucas-Herald A., Bertelloni S., Juul A., Bryce J., Jiang J., Rodie M., et al.

JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, vol.101, no.11, pp.3959-3967, 2016 (Journal Indexed in SCI) identifier identifier identifier

2016

2016

Premature pubarche, hyperinsulinemia, hypothyroxinemia and hyperintensities in basal ganglia: All caused by a single congenital defect

Baş S., GÜRAN T. , Atay Z., Haliloğlu B., Abalı S., Turan S. , et al.

JCRPE Journal of Clinical Research in Pediatric Endocrinology, vol.8, pp.14, 2016 (Journal Indexed in SCI Expanded) identifier

2016

2016

The Etiology and Clinical Features of Non-CAH Gonadotropin-Independent Precocious Puberty: A Multicenter Study

Atay Z., Yesilkaya E., Erdeve S. S. , Turan S. , AKIN L., EREN E., et al.

JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, vol.101, no.5, pp.1980-1988, 2016 (Journal Indexed in SCI) identifier identifier identifier

2016

2016

Reconsideration of Mid-Parental Height Calculation

BEREKET A. , Bugur I. S. , GÜRAN T. , Atay Z., Ekberzade A., Gurbanov Z., et al.

HORMONE RESEARCH IN PAEDIATRICS, vol.86, pp.451, 2016 (Journal Indexed in SCI) identifier

2016

2016

Etiologic Distribution and Characteristics of Patients with Short Stature in a Pediatric Endocrinology Clinic

Ozcan S., Abali S., Atay Z., Haliloglu B., Bas S., Ozturk G., et al.

HORMONE RESEARCH IN PAEDIATRICS, vol.86, pp.457-458, 2016 (Journal Indexed in SCI) identifier

2016

2016

Frequency of Recessive Osteogenesis Imperfecta in a Turkish Cohort and Genetic Causes

Abali S., Arman A. , Atay Z., Bereket A. , Bas S., Haliloglu B., et al.

HORMONE RESEARCH IN PAEDIATRICS, vol.86, pp.175-176, 2016 (Journal Indexed in SCI) identifier

2016

2016

A Novel Animal Model to Study 21-Hydroxylase Deficiency in vivo

Zaucker A., Griffin A., Storbeck K., Guran T. , Thakur N., Weger M., et al.

HORMONE RESEARCH IN PAEDIATRICS, vol.86, pp.70-71, 2016 (Journal Indexed in SCI) identifier

2016

2016

Rare Causes of Primary Adrenal Insufficiency: Genetic and Clinical Characterization of a Large Nationwide Cohort

Guran T. , Buonocore F., Saka N., Ozbek M. N. , Aycan Z., Bereket A. , et al.

JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, vol.101, no.1, pp.283-291, 2016 (Journal Indexed in SCI) identifier identifier identifier

2015

2015

Effect of Maternal Factors and Fetomaternal Glucose Homeostasis on Birth Weight and Postnatal Growth

Askan O. O. , Bozaykut A., Sezer R. G. , GÜRAN T. , BEREKET A.

JOURNAL OF CLINICAL RESEARCH IN PEDIATRIC ENDOCRINOLOGY, vol.7, no.3, pp.168-174, 2015 (Journal Indexed in SCI) identifier identifier identifier

2015

2015

Mutations in LONP1, a Mitochondrial Matrix Protease, Cause CODAS Syndrome

Dikoglu E., Alfaiz A., Gorna M., Bertola D., Chae J. H. , Cho T., et al.

AMERICAN JOURNAL OF MEDICAL GENETICS PART A, vol.167, no.7, pp.1501-1509, 2015 (Journal Indexed in SCI) identifier identifier identifier

2015

2015

Homozygous Loss-of-function Mutations in SOHLH1 in Patients With Nonsyndromic Hypergonadotropic Hypogonadism

Bayram Y., Gulsuner S., GÜRAN T. , ABACI A., Yesil G., Gulsuner H. U. , et al.

JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, vol.100, no.5, 2015 (Journal Indexed in SCI) identifier identifier identifier

2014

2014

Stuve-Wiedemann Syndrome: Is it Underrecognized?

Yesil G., Lebre A. S. , Dos Santos S., Guran O., Ozahi I. I. , Daire V. C. , et al.

AMERICAN JOURNAL OF MEDICAL GENETICS PART A, vol.164, no.9, pp.2200-2205, 2014 (Journal Indexed in SCI) Sustainable Development identifier identifier identifier

2014

2014

Novel Associations in Disorders of Sex Development: Findings From the I-DSD Registry

Cox K., Bryce J., Jiang J., Rodie M., Sinnott R., Alkhawari M., et al.

JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, vol.99, no.2, 2014 (Journal Indexed in SCI) identifier identifier identifier

2013

2013

Infantile loss of teeth: odontohypophosphatasia or childhood hypophosphatasia.

Haliloglu B. , Güran T. , Atay Z., Abali S., Mornet E., Bereket A. , et al.

European journal of pediatrics, vol.172, no.6, pp.851-3, 2013 (Journal Indexed in SCI Expanded) identifier identifier identifier

2013

2013

Five novel mutations in the SCNN1A gene causing autosomal recessive pseudohypoaldosteronism type 1

Welzel M., AKIN L., Buescher A., GÜRAN T. , Hauffa B. P. , Hoegler W., et al.

EUROPEAN JOURNAL OF ENDOCRINOLOGY, vol.168, no.5, pp.707-715, 2013 (Journal Indexed in SCI) Sustainable Development identifier

2012

2012

Mutations in IRX5 impair craniofacial development and germ cell migration via SDF1

Bonnard C., Strobl A. C. , Shboul M., Lee H., Merriman B., Nelson S. F. , et al.

NATURE GENETICS, vol.44, no.6, pp.709-714, 2012 (Journal Indexed in SCI) identifier

2012

2012

A Rare Cause of a Relatively Common Neonatal Emergency

Guran T. , Karasu G. T. , Degirmenci S., Say A., Guran O., Paketci A. T. , et al.

PEDIATRIC HEMATOLOGY AND ONCOLOGY, vol.29, no.4, pp.365-367, 2012 (Journal Indexed in SCI) identifier identifier identifier

2012

2012

Pitfalls in the diagnosis of thyroid dysgenesis by thyroid ultrasonography and scintigraphy

Karakoc-Aydiner E. , Turan S. , Akpinar I., Dede F. , Isguven P., Adal E., et al.

EUROPEAN JOURNAL OF ENDOCRINOLOGY, vol.166, no.1, pp.43-48, 2012 (Journal Indexed in SCI) identifier identifier identifier

2012

2012

A Giant Ovarian Cyst in a Neonate with Classical 21-Hydroxylase Deficiency with Very High Testosterone Levels Demonstrating a High-Dose Hook Effect

GÜRAN T. , Yesil G., Guran O., Cesur S., Bosnali O., Celayir A., et al.

JOURNAL OF CLINICAL RESEARCH IN PEDIATRIC ENDOCRINOLOGY, vol.4, no.3, pp.151-153, 2012 (Journal Indexed in SCI) identifier

2011

2011

International epidemic of childhood obesity and television viewing

Guran T. , Bereket A.

MINERVA PEDIATRICA, vol.63, no.6, pp.483-490, 2011 (Journal Indexed in SCI) Sustainable Development identifier identifier

2011

2011

EFFECT OF BREASTFEEDING ON SERUM ZINC LEVELS AND GROWTH IN HEALTHY INFANTS

Sezer R. G. , Celikel F., Aydemir G., Malbora B., Bayoglu D. S. , Guran T. , et al.

ACTA PAEDIATRICA, vol.100, pp.42-43, 2011 (Journal Indexed in SCI) identifier

2011

2011

Mutations in CYP24A1 and Idiopathic Infantile Hypercalcemia

Schlingmann K. P. , Kaufmann M., Weber S., Irwin A., Goos C., John U., et al.

NEW ENGLAND JOURNAL OF MEDICINE, vol.365, no.5, pp.410-421, 2011 (Journal Indexed in SCI) identifier identifier identifier

2011

2011

Critical Points in the Management of Pseudohypoaldosteronism Type 1

Guran T. , Degirmenci S., Bulut I. K. , Say A., Riepe F. G. , Guran O.

JOURNAL OF CLINICAL RESEARCH IN PEDIATRIC ENDOCRINOLOGY, vol.3, no.2, pp.98-100, 2011 (Journal Indexed in SCI) Creative Commons License Sustainable Development identifier identifier identifier

2011

2011

Cognitive and psychosocial development in children with familial hypomagnesaemia

GÜRAN T. , ARMAN A. , Akcay T., Kayan E., Atay Z., Turan S. , et al.

MAGNESIUM RESEARCH, vol.24, no.1, pp.7-12, 2011 (Journal Indexed in SCI) identifier identifier identifier

2011

2011

Serum Alkaline Phosphatase Levels in Healthy Children and Evaluation of Alkaline Phosphatase z-scores in Different Types of Rickets

Turan S. , Topcu B., Gökce İ. , Güran T. , Atay Z., Omar A., et al.

JOURNAL OF CLINICAL RESEARCH IN PEDIATRIC ENDOCRINOLOGY, vol.3, pp.7-11, 2011 (Journal Indexed in SCI) identifier identifier identifier

2010

2010

Content analysis of food advertising in Turkish television

GÜRAN T. , Turan S. , Akcay T., Degirmenci F., Avci O., Asan A., et al.

JOURNAL OF PAEDIATRICS AND CHILD HEALTH, vol.46, pp.427-430, 2010 (Journal Indexed in SCI) identifier identifier identifier

2009

2009

IRS2 variants and syndromes of severe insulin resistance

Bottomley W. E. , Soos M. A. , Adams C., Guran T. , Howlett T. A. , Mackie A., et al.

DIABETOLOGIA, vol.52, no.6, pp.1208-1211, 2009 (Journal Indexed in SCI) identifier identifier identifier

2009

2009

Cushing's Syndrome Due to a Non-Adrenal Ectopic Adrenocorticotropin-Secreting Ewing's Sarcoma in a Child

GÜRAN T. , Turan S. , Ozkan B., Berrak S. G. , Canpolat C., Dagli T., et al.

JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM, vol.22, no.4, pp.363-368, 2009 (Journal Indexed in SCI) identifier

2009

2009

Alopecia: Association with resistance to thyroid hormones

Güran T. , Bircan R., Turan S. , Bereket A.

Journal of Pediatric Endocrinology and Metabolism, vol.22, no.11, pp.1075-1081, 2009 (Journal Indexed in SCI) identifier identifier identifier

2009

2009

Hypogonadotropic hypogonadism due to a novel missense mutation in the first extracellular loop of the neurokinin B receptor

Guran T. , Tolhurst G., Bereket A. , Rocha N., Porter K., Turan S. , et al.

Journal of Clinical Endocrinology and Metabolism, vol.94, no.10, pp.3633-3639, 2009 (Journal Indexed in SCI) identifier identifier identifier

2009

2009

Cushing's syndrome due to a non-adrenal ectopic adrenocorticotropin- secreting ewing's sarcoma in a child

Güran T. , Turan S., Ozkan B., Berrak S. G. , Canpolat C., Dagli T., et al.

Journal of Pediatric Endocrinology and Metabolism, vol.22, no.4, pp.363-368, 2009 (Journal Indexed in SCI) identifier identifier identifier

2008

2008

Withdrawal of inhaled steroids in children with non-cystic fibrosis bronchiectasis

Guran T. , Ersu R., Karadag B. , Karakoc F., Demirel G. Y. , Hekim N., et al.

JOURNAL OF CLINICAL PHARMACY AND THERAPEUTICS, vol.33, no.6, pp.603-611, 2008 (Journal Indexed in SCI) identifier identifier identifier

2008

2008

Evaluation of diagnosis and treatment results in children with Graves' disease with emphasis on the pubertal status of patients.

Poyrazoǧlu Ş., Saka N., Bas F., Isguven P., Dogu A., Turan S. , et al.

Journal of pediatric endocrinology & metabolism : JPEM, vol.21, no.8, pp.745-51, 2008 (Journal Indexed in SCI Expanded) identifier identifier identifier

2008

2008

Significance of acanthosis nigricans in childhood obesity

Güran T. , Turan S. , Akcay T., Bereket A.

JOURNAL OF PAEDIATRICS AND CHILD HEALTH, vol.44, no.6, pp.338-341, 2008 (Journal Indexed in SCI) Sustainable Development identifier

2008

2008

Alendronate treatment in children with osteogenesis imperfecta

Akcay T., Turan S. , GÜRAN T. , Bereket A.

Indian Pediatrics, vol.45, no.2, pp.105-109, 2008 (Journal Indexed in SCI Expanded) identifier identifier identifier

2008

2008

Constitutional growth delay pattern of growth in velo-cardio-facial syndrome: longitudinal follow up and final height of two cases.

Turan S. , Ozdemir N., Güran T. , Akalin F., Akçay T., Ayabakan C., et al.

Journal of clinical research in pediatric endocrinology, vol.1, no.1, pp.43-8, 2008 (Journal Indexed in SCI Expanded) identifier identifier

2008

2008

Bone mineral density in children with non-cystic fibrosis bronchiectasis

Güran T. , Turan S. , Karadag B. , Ersu R., Karakoc F., Bereket A. , et al.

RESPIRATION, vol.75, no.4, pp.432-436, 2008 (Journal Indexed in SCI) identifier identifier identifier

2008

2008

Genetic testing of Turkish patients with pseudohypoparathyroidism type Ib

Turan S. , Bereket A. , Akin L., Adal E., Akcay T., Güran T. , et al.

HORMONE RESEARCH, vol.70, pp.50, 2008 (Journal Indexed in SCI) identifier

2006

2006

Severe diabetic ketoacidosis: hyperventilation or relative hypoventilation

Turan S. , Guran T. , Topcu B., Akcay T., Bereket A.

PEDIATRIC CRITICAL CARE MEDICINE, vol.7, no.3, pp.291, 2006 (Journal Indexed in SCI) Sustainable Development identifier identifier identifier

2006

2006

Pycnodysostosis: A rare cause of short stature

Akcay T., Guran T. , Turan S. , Bereket A.

HORMONE RESEARCH, vol.65, pp.76, 2006 (Journal Indexed in SCI) identifier

2006

2006

Evaluation of patients with Graves' disease

Poyrazoglu S., Saka N., Bas F., Isguven P., Dogu A., Turan S. , et al.

HORMONE RESEARCH, vol.65, pp.41, 2006 (Journal Indexed in SCI) identifier

2006

2006

Factors associated with obesity in children with hypothalamo-pituitary tumors

Turan S. , Bereket A. , Guran T. , Akcay T., Gunoz H., Saka N., et al.

HORMONE RESEARCH, vol.65, pp.83, 2006 (Journal Indexed in SCI) Sustainable Development identifier

2006

2006

Compliance with treatment and follow-up in a pediatric obesity clinic

Turan S. , Guran T. , Akcay T., Ay P. , Tekin A., Alkan E., et al.

HORMONE RESEARCH, vol.65, pp.86, 2006 (Journal Indexed in SCI) Sustainable Development identifier

2004

2004

Increased QT dispersion in breath-holding spells

Akalin F. , Turan S. , Guran T. , Ayabakan C., Yilmaz Y.

ACTA PAEDIATRICA, vol.93, no.6, pp.770-774, 2004 (Journal Indexed in SCI) identifier identifier identifier

2003

2003

Oral bisphosphonate therapy for vitamin D intoxication of the infant.

Bereket A. , Erdogan T.

Pediatrics, vol.111, no.4 Pt 1, pp.899-901, 2003 (Journal Indexed in SCI Expanded) identifier identifier identifier

Articles Published in Other Journals

2019

2019

Frequency of Ambiguous Genitalia in 14,177 Newborns in Turkey

Aydin B. K. , Saka N., Baş F., Bas E. K. , Çoban E. A. , Yildirim S., et al.

Journal of the Endocrine Society, vol.3, no.6, pp.1185-1195, 2019 (Journal Indexed in ESCI) identifier identifier identifier

2016

2016

Risk factors for mortality caused by hypothalamic obesity in children with hypothalamic tumours.

Haliloglu B. , Atay Z., Guran T. , Abali S., Bas S., Turan S. , et al.

Pediatric obesity, vol.11, no.5, pp.383-8, 2016 (Refereed Journals of Other Institutions) Sustainable Development identifier identifier identifier

Refereed Congress / Symposium Publications in Proceedings

2021

2021

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

2021

2021

Optimizing medical therapy in congenital adrenal hyperplasia

Güran T.

Indonesian Congress of Pediatrics (KONIKA 2021), 15 October - 19 December 2021, pp.1-3

2021

2021

Common and rare adrenal causes of DSD

Güran T.

DSD SIG Programme , 08 October 2021, pp.1-2

2021

2021

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

2021

2021

46,XX cinsiyet gelisim bozukluklarina yaklasim

Güran T.

XXV. Ulusal Pediatrik Endokrinoloji ve Diyabet Kongresi, Antalya, Turkey, 6 - 10 October 2021, pp.2-3

2021

2021

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

2021

2021

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

2021

2021

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

2021

2021

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

2021

2021

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

2021

2021

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

2021

2021

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

2021

2021

KONJENİTAL ADRENAL HİPERPLAZİNİN YÖNETİMİ

Güran T.

VI. Pediatrik Endokrinoloji İleri Kursu, İstanbul, Turkey, 11 - 13 June 2021, pp.1-3

2021

2021

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

2021

2021

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

2021

2021

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

2021

2021

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

2021

2021

Cocuklarda gecikmis puberte

Güran T.

Endokrinoloji Talim, Baku, Azerbaijan, 3 - 04 April 2021, pp.1-2

2021

2021

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

2021

2021

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

2021

2021

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

2021

2021

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

2021

2021

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

2021

2021

Steroidogenezde Arka Yolak Hastalıklarının Klinik Yansımaları

Güran T.

4. Ege Endokrin Hastalıklar ve Genetik Sempozyumu, İzmir, Turkey, 12 - 13 March 2021, pp.1-2

2021

2021

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

2021

2021

Konjenital Adrenal Hiperplazi Tanısında Zorluklar

Güran T.

Endokrin Hastalıkların Genetiği Seminerleri, İzmir, Turkey, 29 January 2021, pp.1-2

2020

2020

46, XX Cinsiyet gelişim bozukluklarına yaklaşım

Güran T.

VI. PEDİATRİK ENDOKRİNOLOJİYE GİRİŞ KURSU, İstanbul, Turkey, 21 - 22 November 2020, pp.1-2

2020

2020

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

2020

2020

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

2020

2020

Adrenal Yetmezlik ve Yönetimi

Güran T.

Çocuk Endokrinolojisinde Güncellemeler, İstanbul, Turkey, 18 - 19 September 2020, pp.1-2

2020

2020

ESPE DSD WG UPDATE

GÜRAN T.

I-DSD/CAH User Group Meeting, 9 September 2020 (webinar), England, 09 September 2020

2020

2020

Endokrin Söyleşiler-Yeni Gen Keşfinde Yolculuk

Güran T.

24. Ulusal Pediatrik Endokrinoloji ve Diyabet Kongresi, İstanbul, Turkey, 15 - 19 April 2020, pp.1-2

2019

2019

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

2019

2019

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

2019

2019

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 identifier identifier identifier

2019

2019

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

2019

2019

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

2019

2019

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

2018

2018

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

2018

2018

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

2018

2018

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

2018

2018

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

2018

2018

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

2018

2018

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

2018

2018

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

2017

2017

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

2017

2017

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

2017

2017

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

2017

2017

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

2017

2017

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

2017

2017

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

2017

2017

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

2017

2017

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

2017

2017

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

2017

2017

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

2017

2017

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

2017

2017

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, England, 6 - 09 September 2017, vol.32, pp.1744

2017

2017

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

2017

2017

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

2017

2017

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

2017

2017

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

2017

2017

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

2016

2016

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

2016

2016

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

2016

2016

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

2016

2016

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

2016

2016

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

2016

2016

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

2015

2015

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

2015

2015

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

2015

2015

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

2015

2015

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 Sustainable Development

2015

2015

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

2015

2015

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

2015

2015

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

2015

2015

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

2015

2015

Idrar steroid profili

Güran T.

XIX. ULUSAL PEDIATRIK ENDOKRINOLOJI KONGRESI, İstanbul, Turkey, 20 - 22 October 2015

2015

2015

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

2015

2015

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

2015

2015

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

2015

2015

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

2015

2015

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

2015

2015

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 Sustainable Development

2015

2015

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 Sustainable Development

2015

2015

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

2015

2015

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

2007

2007

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 identifier

2006

2006

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

Books & Book Chapters

2021

2021

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

2021

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 Sustainable Development

2021

2021

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 Sustainable Development

2021

2021

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 Sustainable Development

2019

2019

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

2019

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

2019

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

2018

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

2017

Adrenal hastaliklar

Güran T.

in: Yurdakok Pediatri, Murat Yurdakok, Editor, Gunes Tip Kitapevleri, İstanbul, pp.4142-4154, 2017

2017

2017

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

2016

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

2014

Cinsiyet Gelisim Bozuklugu

Güran T.

in: Cocuk Endokrinolojisinde Uzlasi, NA, Editor, Nobel Yayincilik, İstanbul, pp.75-98, 2014

2014

2014

Yenidogan KAH taramalari, prenatal tani ve tedavi

Güran T. , Ozsu E.

in: Cocuk Endokrinolojisinde Uzlasi, NA, Editor, Nobel Yayincilik., İstanbul, pp.103-106, 2014

2013

2013

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

2012

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

2012

2012

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

2010

2010

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

Activities in Scientific Journals

2021 - Continues

2021 - Continues

Hormone Research In Paediatrics

Special Issue Editor

Memberships / Tasks in Scientific Organizations

2021 - Continues

2021 - Continues

Turk Cocuk Endokrinolojisi ve Diyabet Dernegi Adrenal Calisma GrubuSustainable Development

Vice President

2020 - Continues

2020 - Continues

I-DSD Steering Committee

Member

2020 - Continues

2020 - Continues

Turk Cocuk Endokrinoloji ve Diyabet DernegiSustainable Development

Secretary General

2019 - Continues

2019 - Continues

European society of pediatric endocrinology DSD working group

Chairman

2018 - Continues

2018 - Continues

European Society of Pediatric Endocrinology Science Committee Expert Panel

Member

Scientific Refereeing

October 2021

October 2021

JOURNAL OF PEDIATRICS

Journal Indexed in SCI-E

September 2021

September 2021

JOURNAL OF CLINICAL RESEARCH IN PEDIATRIC ENDOCRINOLOGY

Journal Indexed in SCI-E

July 2021

July 2021

EUROPEAN JOURNAL OF ENDOCRINOLOGY

Journal Indexed in SCI-E

March 2021

March 2021

JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM

Journal Indexed in SCI-E

February 2021

February 2021

JOURNAL OF CLINICAL RESEARCH IN PEDIATRIC ENDOCRINOLOGY

Journal Indexed in SCI-E

Awards

October 2021

October 2021

Yilin en iyi yayin odulu

Turk Cocuk Endokrinoloji Ve Diyabet Dernegi

October 2021

October 2021

Sozel sunum ucunculuk odulu

Turk Cocuk Endokrinoloji Ve Diyabet Dernegi

September 2021

September 2021

People`s choice poster awardSustainable Development

European Society Of Pediatric Endocrinology

February 2021

February 2021

Dr Tolga Koroglu ozel odulu

8. Marmara Pediatri Kongresi

November 2020

November 2020

Kısa 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 2020

Sözlu 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 2020

Poster Bildiri Birincilik Ödülü-Parsiyel Pankreatik Agenezi ve Sendromik Hipopituarizm

Xxıv. Ulusal Pediatrik Endokrinoloji Ve Diyabet Çevrim İçi Kongresi

October 2013

October 2013

Best second oral presentation

Ulusal Pediatrik Endokrinoloji Kongresi Bilimsel Kurul



Edit Congress and Symposium Activities

2021

2021

NovoCME Continuous Medical Education International Academy online

Moderator

İstanbul-Turkey

2021

2021

XXV. Ulusal Pediatrik Endokrinoloji ve Diyabet KongresiSustainable Development

Session Moderator

Antalya-Turkey

2021

2021

European Society for Paediatric Endocrinology 2021 meeting

Moderator

Liverpool-England

2021

2021

8th I-DSD Symposium 2021

Session Moderator

Glasgow-England

2021

2021

10.Olgu Sunumları Sempozyumu

Session Moderator

İzmir-Turkey

Invited Talks

November 2021

November 2021

Türkiye`de Konjenital Adrenal Hiperplazi Yenidoğan Taraması: Verilerin Değerlendirilmesi

Conference

65. Türkiye Milli Pediatri Kongresi-Turkey

October 2021

October 2021

Steroidogenezde Aberan Androjen Üretimi ve Klinik Yansımaları

Seminar

XXV. Ulusal Pediatrik Endokrinoloji ve Diyabet Kongresi-Turkey

October 2021

October 2021

Common and rare adrenal causes of DSD

Seminar

BSPED DSD SIG Programme -England

October 2021

October 2021

46,XX cinsiyet gelisim bozukluklarina yaklasim

Seminar

XXV. Ulusal Pediatrik Endokrinoloji ve Diyabet Kongresi-Turkey

October 2021

October 2021

Optimizing Medical Therapy in Different Forms of Congenital Adrenal Hyperplasia

Seminar

KONIKA XVIII Medan 2021-Indonesia

June 2021

June 2021

KONJENİTAL ADRENAL HİPERPLAZİNİN YÖNETİMİ

Seminar

VI. Pediatrik Endokrinoloji İleri Kursu-Turkey

May 2021

May 2021

Optimizing 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 2021

Cocuklarda gecikmis ergenlik

Seminar

Endokrinoloji Talim-Turkey

March 2021

March 2021

Steroidogenezde Arka Yolak Hastalıklarının Klinik Yansımaları

Seminar

4. Ege Endokrin Hastalıklar ve Genetik Sempozyumu-Turkey

January 2021

January 2021

Konjenital Adrenal Hiperplazi Tanısında Zorluklar

Seminar

Endokrin Hastalıkların Genetiği Seminerleri-Turkey

November 2020

November 2020

46, XX Cinsiyet gelişim bozukluklarına yaklaşım

Seminar

VI. PEDİATRİK ENDOKRİNOLOJİYE GİRİŞ KURSU -Turkey

October 2020

October 2020

Geç tanı alan Turner sendromu olgusunda büyüme hormonu tedavisi ve puberte induksiyonu

Seminar

NordiPEVA Büyüyen Tecrübe Toplantısı-Turkey

September 2020

September 2020

Adrenal Yetmezlik ve Yönetimi

Seminar

Çocuk Endokrinolojisinde Güncellemeler-Turkey

April 2020

April 2020

Endokrin Söyleşiler-Yeni Gen Keşfinde Yolculuk

Seminar

24. Ulusal Pediatrik Endokrinoloji ve Diyabet Kongresi-Turkey

Scholarships

2021 - 2021

2021 - 2021

Registration Grant

Other International Organizations

2021 - 2021

2021 - 2021

Registration grant

Other International Organizations

2021 - 2021

2021 - 2021

Registration grant

Other International Organizations

Citations

Total Citations (WOS): 2131

h-index (WOS): 24

Jury Memberships

November-2021

November 2021

Expertise In Medicine

Expertise In Medicine - Marmara Üniversitesi

August-2021

August 2021

Appointment Academic Staff

Appointment Academic Staff - Koç Üniversitesi

July-2021

July 2021

Expertise In Medicine

Expertise In Medicine - Marmara Üniversitesi

May-2021

May 2021

Associate Professor Exam

Associate Professor Exam - Sağlık Bilimleri Üniversitesi

April-2021

April 2021

Expertise In Medicine

Expertise In Medicine - Marmara Üniversitesi

March-2021

March 2021

Appointment Academic Staff

Appointment Academic Staff - Sağlık Bilimleri Üniversitesi

February-2021

February 2021

Appointment Academic Staff

Appointment Academic Staff - Sağlık Bilimleri Üniversitesi

February-2021

February 2021

Appointment Academic Staff

Appointment Academic Staff - Sağlık Bilimleri Üniversitesi

March-2020

March 2020

Associate Professor Exam

Associate Professor Exam - Marmara Üniversitesi

March-2020

March 2020

Appointment Academic Staff

Appointment Academic Staff - İstanbul Aydın Üniversitesi

December-2019

December 2019

Appointment Academic Staff

Appointment Academic Staff - Altınbaş Üniversitesi

March-2019

March 2019

Associate Professor Exam

Associate Professor Exam - Marmara Üniversitesi

November-2018

November 2018

Appointment Academic Staff

Appointment Academic Staff - Koç Üniversitesi

December-2017

December 2017

Associate Professor Exam

Associate Professor Exam - Marmara Üniversitesi

October-2017

October 2017

Associate Professor Exam

Associate Professor Exam - Pamukkale Üniversitesi