Prof. Dr. SERAP DEMİRCİOĞLU

Yayın Ağı

Makaleler 274

1. Impact of Growth-promoting Therapies on Puberty, Growth, and Final Height in Classical 21-hydroxylase Deficiency.

Yavas Abali Z., Yildiz M., Abali S., Moniri A., Bas F., Onal H., et al.

The Journal of clinical endocrinology and metabolism , 2025 (SCI-Expanded, Scopus)

2. The Mystery of Elevated β-hCG in GnRH-Independent Precocious Puberty without a Detectable Tumor: A Six-Year Diagnostic Odyssey.

Helvacioglu D., Akberzade A., Abali S., Almus E., Atay Z., Guran T., et al.

Hormone research in paediatrics , ss.1-15, 2025 (SCI-Expanded, Scopus)

3. Mapping variants in thyroid hormone transporter MCT8 to disease severity by genomic, phenotypic, functional, structural and deep learning integration

Groeneweg S., van Geest F. S., Martín M., Dias M., Frazer J., Medina-Gomez C., et al.

Nature Communications , cilt.16, sa.1, 2025 (SCI-Expanded, Scopus)

4. Transition Care for Young Persons with Rare Bone Mineral Conditions: A Consensus Recommendation from the ECTS Rare Bone Disease Action Group

Grasemann C., Wernsmann J., Appelman-Dijkstra N. M., Morgan C., Sylvest T. T., Raimann A., et al.

Calcified Tissue International , cilt.116, sa.1, 2025 (SCI-Expanded, Scopus)

5. Clinical and Molecular Spectrum of Infantile Hypercalcemia Type I: Insights Into CYP24A1 Variants.

Eltan M., Alavanda C., Kurt İ., Yavas Abali Z., Abali S., Helvacioglu D., et al.

Clinical endocrinology , 2025 (SCI-Expanded, Scopus)

6. Isolated Hypoglyceamia in Children with Cystic Fibrosis: Role of Pancreatic Insufficiency and Glucagon Response.

Haliloglu B., Seven Menevse T., Gulec Yilmaz S., Akdeniz T., Gurpinar Tosun B., Demircioglu S., et al.

Journal of clinical research in pediatric endocrinology , 2025 (SCI-Expanded, Scopus, TRDizin)

7. Clinical and Molecular Genetic Characteristics of Patients with Hereditary Hypophosphatemia.

Eltan M., Alavanda C., Abali Z., Tosun B. G., Kurt I., Kirkgoz T., et al.

The Journal of clinical endocrinology and metabolism , cilt.110, sa.9, 2025 (SCI-Expanded, Scopus)

8. Genotype, Phenotype Characteristics and Long-Term Follow-Up of Patients with Vitamin D-Dependent Rickets Type IA: A Nationwide Multi-Centre Retrospective Cross-Sectional Study.

Cayir A., Demirbilek H., Türkyılmaz A., Turan S., Bereket A., Darendeliler F., et al.

Hormone research in paediatrics , ss.1-9, 2025 (SCI-Expanded, Scopus)

9. Expanding the Clinical Features of Schimke Immuno-Osseous Dysplasia: A New Patient with a Novel Variant and Novel Clinical Findings.

Alavanda C., Demir Ş., Güven S., Eltan M., Bilgiç Eltan S., Sefer A. P., et al.

Journal of clinical research in pediatric endocrinology , cilt.17, ss.126-135, 2025 (SCI-Expanded, Scopus, TRDizin)

10. Optimal Low-Dose Synacthen Stimulation Test Sampling Time for Diagnosis of Adrenal Insufficiency Using Monoclonal Antibody Immunoassay.

Tosun B. G., Turan S., Haklar G., Bereket A., Guran T.

Hormone research in paediatrics , ss.1-8, 2025 (SCI-Expanded, Scopus)

11. Relation of Serum IGF-1 and IGFBP-3 Levels with Acute Exacerbation in Cystic Fibrosis

Eser A. F., ERDEM ERALP E., GÖKDEMİR Y., ERGENEKON A. P., DEMİRCİOĞLU S., AY N. P., et al.

Journal of Pediatric Research , cilt.12, sa.1, ss.1-6, 2025 (ESCI)

12. 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 , cilt.38, sa.3, ss.201-206, 2025 (SCI-Expanded)

13. Evaluation of Growth Characteristics and Final Heights of Cases Diagnosed with Noonan Syndrome on GH Treatment.

Şıklar Z., Berberoğlu M., Kızılcan Çetin S., Yıldız M., Turan S., Darcan Ş., et al.

Journal of clinical research in pediatric endocrinology , cilt.17, ss.76-86, 2025 (SCI-Expanded, Scopus, TRDizin)

14. Real-life experience on efficacy and safety of setmelanotide treatment in prepubertal children

Kahveci A., Kurt I., Turan S., Guran T., Bereket A., Haliloglu B.

EUROPEAN JOURNAL OF ENDOCRINOLOGY , cilt.192, sa.2, 2025 (SCI-Expanded)

15. Presentation and outcome in carriers of pathogenic variants in SLC34A1 and SLC34A3 encoding sodium-phosphate transporter NPT 2a and 2c.

Brunkhorst M., Brunkhorst L., Martens H., Papizh S., Besouw M., Grasemann C., et al.

Kidney international , cilt.107, sa.1, ss.116-129, 2025 (SCI-Expanded, Scopus)

16. Pediatric osteoporosis: An update

Günay A., DEMİRCİOĞLU S.

Trends in Pediatrics , cilt.5, sa.4, ss.105-115, 2024 (Scopus)

17. Global burden of disease attributable to metabolic risk factors in adolescents and young adults aged 15-39, 1990-2021.

Zhou X., Chen Q., Targher G., Byrne C. D., Mantzoros C. S., Zhang H., et al.

Clinical nutrition (Edinburgh, Scotland) , cilt.43, sa.12, ss.391-404, 2024 (SCI-Expanded, Scopus)

18. A global survey on the use of the international classification of diseases codes for metabolic dysfunction-associated fatty liver disease

Zhang H., Targher G., Byrne C. D., Kim S. U., Wong V. W., Valenti L., et al.

Hepatology International , cilt.18, sa.4, ss.1178-1201, 2024 (SCI-Expanded, Scopus)

19. An international multidisciplinary consensus on pediatric metabolic dysfunction-associated fatty liver disease

Zhang L., El-Shabrawi M., Baur L. A., Byrne C. D., Targher G., Kehar M., et al.

Med , cilt.5, sa.7, ss.797, 2024 (ESCI, Scopus)

20. 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 , cilt.54, sa.7, ss.1156-1167, 2024 (SCI-Expanded)

21. 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 , cilt.183, sa.3, ss.1325-1332, 2024 (SCI-Expanded, Scopus)

22. 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 , cilt.97, sa.4, ss.404-415, 2024 (SCI-Expanded, Scopus)

23. 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 , cilt.96, sa.5, ss.527-537, 2023 (SCI-Expanded, Scopus)

24. Two new cases with novel pathogenic variants reflecting the clinical diversity of Schaaf-Yang syndrome

ALAVANDA C., Arslan Ateş E., Yavaş Abalı Z., GEÇKİNLİ B. B., DEMİRCİOĞLU S., ARMAN A.

Clinical Genetics , cilt.104, sa.1, ss.127-132, 2023 (SCI-Expanded, Scopus) Sürdürülebilir Kalkınma

25. 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 , cilt.15, sa.2, ss.154-159, 2023 (SCI-Expanded, Scopus, TRDizin)

26. 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 , cilt.36, sa.4, ss.401-408, 2023 (SCI-Expanded, Scopus)

27. Osteopetrosis: Gene-based nosology and significance dysosteosclerosis.

Turan S.

Bone , cilt.167, 2023 (SCI-Expanded, Scopus)

28. Liraglutide for Weight Management in Children and Adolescents With Prader-Willi Syndrome and Obesity

Diene G., Angulo M., Hale P. M., Jepsen C. H., Hofman P. L., Hokken-Koelega A., et al.

JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM , cilt.108, ss.4-12, 2022 (SCI-Expanded, Scopus)

29. 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 , cilt.95, sa.SUPPL 2, ss.46-47, 2022 (SCI-Expanded)

30. A Case of Short Stature Presenting with Multiple Exocytosis

Kaygusuz S. B., Gokoglu M., DEMİRCİOĞLU S.

HORMONE RESEARCH IN PAEDIATRICS , cilt.95, sa.SUPPL 2, ss.318, 2022 (SCI-Expanded)

31. 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 , cilt.95, sa.SUPPL 2, ss.364, 2022 (SCI-Expanded)

32. 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 , cilt.95, sa.SUPPL 2, ss.407, 2022 (SCI-Expanded) Sürdürülebilir Kalkınma

33. 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 , cilt.95, sa.SUPPL 2, ss.230, 2022 (SCI-Expanded)

34. 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 , cilt.95, sa.SUPPL 2, ss.213, 2022 (SCI-Expanded) Sürdürülebilir Kalkınma

35. 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 , cilt.95, sa.SUPPL 2, ss.377-378, 2022 (SCI-Expanded)

36. 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 , cilt.95, sa.SUPPL 2, ss.141-142, 2022 (SCI-Expanded)

37. 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 , cilt.95, sa.SUPPL 2, ss.231-232, 2022 (SCI-Expanded) Sürdürülebilir Kalkınma

38. 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 , cilt.95, sa.SUPPL 2, ss.199-200, 2022 (SCI-Expanded)

39. 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 , cilt.95, sa.SUPPL 2, ss.139, 2022 (SCI-Expanded)

40. 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 , cilt.95, sa.SUPPL 2, ss.566, 2022 (SCI-Expanded)

41. 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 , cilt.95, sa.SUPPL 2, ss.117-118, 2022 (SCI-Expanded)

42. Genotype, phenotype characteristics and long-term follow-up of patients with Vitamin D Dependent Rickets Type IA (VDDR1a): A nationwide multicentre retrospective cross-sectional study

Cayir A., DEMİRBİLEK H., TÜRKYILMAZ A., DEMİRCİOĞLU S., BEREKET A., Darendeliler F., et al.

HORMONE RESEARCH IN PAEDIATRICS , cilt.95, sa.SUPPL 2, ss.100, 2022 (SCI-Expanded)

43. 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 , cilt.6, sa.8, 2022 (ESCI)

44. 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 , cilt.92, sa.1, ss.265-274, 2022 (SCI-Expanded, Scopus)

45. 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 , cilt.16, sa.SUPPL 1, ss.61-62, 2022 (SCI-Expanded)

46. RASopatilerin Moleküler Genetik Özellikleri

Yavaş Abalı Z., Demircioğlu S.

Türkiye Klinikleri Pediatri Dergisi , cilt.1, sa.1, ss.14-24, 2022 (Hakemsiz Dergi)

47. 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 , cilt.110, sa.4, ss.441-450, 2022 (SCI-Expanded, Scopus)

48. 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 , cilt.157, 2022 (SCI-Expanded) Sürdürülebilir Kalkınma

49. 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 , cilt.107, 2022 (SCI-Expanded, Scopus)

50. 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 , cilt.186, sa.5, 2022 (SCI-Expanded, Scopus)

51. Lack of GNAS re-methylation during oogenesis may be a cause of sporadic pseudohypoparathyroidism type Ib (PHP1B).

Milioto A., Reyes M., Hanna P., Kiuchi Z., Turan S., Zeve D., et al.

The Journal of clinical endocrinology and metabolism , cilt.107, 2022 (SCI-Expanded, Scopus)

52. 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 , cilt.14, ss.10-16, 2022 (SCI-Expanded, Scopus, TRDizin)

53. Long-term efficacy of T3 analogue Triac in children and adults with MCT8 deficiency: a real-life retrospective cohort study.

Van Geest F. S., Groeneweg S., Van Den Akker E. L. T., Bacos I., Barca D., Van Den Berg S. A. A., et al.

The Journal of clinical endocrinology and metabolism , cilt.107, 2022 (SCI-Expanded, Scopus)

54. 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 , cilt.186, ss.65-72, 2022 (SCI-Expanded, Scopus)

55. 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 , cilt.107, 2022 (SCI-Expanded)

56. 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 , sa.4, 2021 (SCI-Expanded)

57. 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 , cilt.106, sa.10, 2021 (SCI-Expanded)

58. 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 , cilt.94, sa.SUPPL 1, ss.107, 2021 (SCI-Expanded)

59. Acetazolamide treatment in a patient with pseudohypoparathyroidism with venous calcification

Seven Menevşe T., Gürpınar Tosun B., Abali Z. Y., Helvacioglu D., Kaygusuz S. B., Eltan M., et al.

HORMONE RESEARCH IN PAEDIATRICS , cilt.94, sa.SUPPL 1, ss.75, 2021 (SCI-Expanded)

60. 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 , cilt.94, sa.SUPPL 1, ss.75, 2021 (SCI-Expanded)

61. Genotypic Sex and Severity of the Disease Determine the Time of Clinical Presentation in Steroid 17 alpha-Hydroxylase/17,20-Lyase Deficiency

Kurnaz E., Baykan E. K., Turkyilmaz A., Yarali O., Abali Z. Y., Demircioğlu S., et al.

HORMONE RESEARCH IN PAEDIATRICS , cilt.94, sa.SUPPL 1, ss.191, 2021 (SCI-Expanded)

62. 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 , cilt.94, sa.SUPPL 1, ss.364, 2021 (SCI-Expanded)

63. Clinical and hormonal evolution of aldosterone synthase deficiency: Is complete remission possible?

Gürpınar Tosun B., Demirkol Y. K., Seven Menevşe T., Kaygusuz S. B., Ozbek M. N., Altıncık S. A., et al.

HORMONE RESEARCH IN PAEDIATRICS , cilt.94, sa.SUPPL 1, ss.184-185, 2021 (SCI-Expanded)

64. Correlation of 11-oxygenated C19 androgens with the clinical and biochemical characteristics in premature adrenarche

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

HORMONE RESEARCH IN PAEDIATRICS , cilt.94, sa.SUPPL 1, ss.120-121, 2021 (SCI-Expanded)

65. Endocrine disrupting chemicals and bone.

Turan S.

Best practice & research. Clinical endocrinology & metabolism , cilt.35, 2021 (SCI-Expanded, Scopus)

66. Severe Hypophosphatemic Rickets due to Tumor-Induced Osteomalasia

HALİLOĞLU B., Pehlivan E., Yilmaz D., Cift H. T., Tasdelen N., Sav A., et al.

HORMONE RESEARCH IN PAEDIATRICS , cilt.94, sa.SUPPL 1, ss.209, 2021 (SCI-Expanded)

67. 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 , cilt.94, sa.SUPPL 1, ss.359, 2021 (SCI-Expanded)

68. 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 , cilt.94, sa.SUPPL 1, ss.275, 2021 (SCI-Expanded) Sürdürülebilir Kalkınma

69. Adrenocortical hormone profiles do not predict the molecular etiology in non-CAH primary adrenal insufficiency

Seven Menevşe T., Demirkol Y. K., Gürpınar Tosun B., Bayramoglu E., Yildiz M., Acar S., et al.

HORMONE RESEARCH IN PAEDIATRICS , cilt.94, sa.SUPPL 1, ss.64-65, 2021 (SCI-Expanded)

70. 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 , cilt.94, sa.SUPPL 1, ss.393-394, 2021 (SCI-Expanded)

71. 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 , cilt.94, sa.SUPPL 1, ss.92, 2021 (SCI-Expanded)

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

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

JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM , cilt.106, sa.9, 2021 (SCI-Expanded, Scopus)

73. 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 , cilt.106, sa.7, 2021 (SCI-Expanded, Scopus)

74. Does Genotype–Phenotype Correlation Exist in Vitamin D-Dependent Rickets Type IA: Report of 13 New Cases and Review of the Literature

Kaygusuz S. B., Alavanda C., Kırkgöz T., Eltan M., Yavas Abali Z., Helvacioglu D., et al.

Calcified Tissue International , cilt.108, sa.5, ss.576-586, 2021 (SCI-Expanded, Scopus)

75. Is quail egg a potential endocrine disrupter?

Sürekli Karakuş Ö., Arabacı Tamer S., Levent H. N., Kaygusuz S. B., Demircioğlu S., Akakın D., et al.

NEUROENDOCRINOLOGY , cilt.111, ss.32, 2021 (SCI-Expanded)

76. Use of Insulin Degludec/Insulin Aspart in the Management of Diabetes Mellitus: Expert Panel Recommendations on Appropriate Practice Patterns

Demir T., Demircioğlu S., Ünlühizarcı K., Topaloglu O., Tukek T., Yavuz D.

FRONTIERS IN ENDOCRINOLOGY , cilt.12, 2021 (SCI-Expanded, Scopus) Sürdürülebilir Kalkınma

77. Cinacalcet as a First-Line Treatment in Neonatal Severe Hyperparathyroidism Secondary to Calcium Sensing Receptor (CaSR) Mutation

Gulcan-Kersin S., Kirkgoz T., Eltan M., Rzayev T., Ata P., Bilgen H. S., et al.

HORMONE RESEARCH IN PAEDIATRICS , cilt.93, sa.5, ss.313-321, 2020 (SCI-Expanded)

78. Persistent Mullerian Duct Syndrome: A Rare But Important Etiology of Inguinal Hernia and Cryptorchidism

Bugrul F., Abali Z., Kırkgöz T., Karadeniz Cerit K., Canmemiş A., Demircioğlu S., et al.

SEXUAL DEVELOPMENT , cilt.13, ss.264-270, 2020 (SCI-Expanded, Scopus)

79. Recommendations for Diagnosis and Treatment of Pseudohypoparathyroidism and Related Disorders: An Updated Practical Tool for Physicians and Patients

Mantovani G., Bastepe M., Monk D., De Sanctis L., Thiele S., Ahmed S. F., et al.

HORMONE RESEARCH IN PAEDIATRICS , cilt.93, sa.3, ss.182-196, 2020 (SCI-Expanded, Scopus) Sürdürülebilir Kalkınma

80. Disease characteristics of MCT8 deficiency: an international, retrospective, multicentre cohort study

Groeneweg S., Van Geest F. S., Abacı A., Alcantud A., Ambegaonkar G. P., Armour C. M., et al.

LANCET DIABETES & ENDOCRINOLOGY , cilt.8, sa.7, ss.594-605, 2020 (SCI-Expanded, Scopus)

81. Management of Systemic Hypersensitivity Reactions to Gonadotropin-Releasing Hormone Analogues during Treatment of Central Precocious Puberty

Kirkgoz T., Karakoc-Aydiner E., Bugrul F., Yavas Abali Z., Helvacioglu D., Kiykim A., et al.

HORMONE RESEARCH IN PAEDIATRICS , cilt.93, sa.1, ss.66-72, 2020 (SCI-Expanded, Scopus)

82. A Rare Cause of Hypophosphatemia: Raine Syndrome Changing Clinical Features with Age

Eltan M., Alavanda C., Yavas Abali Z., Ergenekon P., Yalindag Ozturk N., Sakar M., et al.

CALCIFIED TISSUE INTERNATIONAL , cilt.107, ss.96-103, 2020 (SCI-Expanded, Scopus)

83. 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 , cilt.12, sa.2, ss.150-159, 2020 (SCI-Expanded, Scopus, TRDizin)

84. Clinical Significance of Hypophosphatasemia in Children

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

CALCIFIED TISSUE INTERNATIONAL , cilt.106, sa.6, ss.608-615, 2020 (SCI-Expanded, Scopus) Sürdürülebilir Kalkınma

85. Once-Weekly Somapacitan vs Daily GH in Children With GH Deficiency: Results From a Randomized Phase 2 Trial

Sävendahl L., Battelino T., Brod M., Rasmussen M. H., Horikawa R., Juul R. V., et al.

JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM , cilt.105, sa.4, 2020 (SCI-Expanded, Scopus)

86. Hereditary vitamin D-resistant rickets: a report of four cases with two novel variants in the VDR gene and successful use of intermittent intravenous calcium via a peripheral route

Abali S., Tamura M., DEMİRCİOĞLU S., Atay Z., Isguven P., GÜRAN T., et al.

JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM , cilt.33, sa.4, ss.557-562, 2020 (SCI-Expanded)

87. 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 , cilt.105, sa.4, 2020 (SCI-Expanded, Scopus)

88. Fibroblast Growth Factor-23 and Matrix Extracellular Phosphoglycoprotein Levels in Healthy Children and, Pregnant and Puerperal Women

Ozsen A., Furman A., Güran T., Bereket A., Demircioğlu S.

HORMONE RESEARCH IN PAEDIATRICS , cilt.92, sa.5, ss.302-310, 2020 (SCI-Expanded) Sürdürülebilir Kalkınma

89. Low DHEAS Concentration in a Girl Presenting with Short Stature and Premature Pubarche: A Novel PAPSS2 Gene Mutation

Eltan M., Yavas Abali Z., Arslan Ates E., Kırkgöz T., Kaygusuz S. B., Türkyllmaz A., et al.

Hormone Research in Paediatrics , cilt.92, sa.4, ss.262-268, 2020 (SCI-Expanded, Scopus)

90. Rapid progression of type 2 diabetes and related complications in children and young people-A literature review

Barrett T., Jalaludin M. Y., DEMİRCİOĞLU S., Hafez M., Shehadeh N.

PEDIATRIC DIABETES , cilt.21, sa.2, 2020 (SCI-Expanded, Scopus) Sürdürülebilir Kalkınma

91. 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 , cilt.35, sa.3, ss.403-404, 2020 (SCI-Expanded, Scopus)

92. 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 , cilt.35, sa.3, ss.405-407, 2020 (SCI-Expanded, Scopus)

93. 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 , cilt.92, sa.3, ss.203-208, 2020 (SCI-Expanded)

94. Recommendations for improving clinical trial design to facilitate the study of youth-onset type 2 diabetes

Jalaludin M. Y., Barrientos-Pérez M., Hafez M., Lynch J., Shehadeh N., Turan S., et al.

Clinical Trials , cilt.17, sa.1, ss.87-98, 2020 (SCI-Expanded) Sürdürülebilir Kalkınma

95. GUIDELINES ON THE DIAGNOSIS AND MANAGEMENT OF X-LINKED HYPOPHOSPHATEMIA

Demircioğlu S.

JOURNAL OF ISTANBUL FACULTY OF MEDICINE-ISTANBUL TIP FAKULTESI DERGISI , cilt.83, 2020 (ESCI)

96. PREFACE

Darendeliler F., DEMİRCİOĞLU S.

JOURNAL OF ISTANBUL FACULTY OF MEDICINE-ISTANBUL TIP FAKULTESI DERGISI , cilt.83, 2020 (ESCI)

97. A rare cause of hypertension in childhood: Questions

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

PEDIATRIC NEPHROLOGY , cilt.35, sa.1, ss.77-78, 2020 (SCI-Expanded, Scopus)

98. Genotypic Sex and Severity of the Disease Determine the Time of Clinical Presentation in Steroid 17α-Hydroxylase/17,20-Lyase Deficiency.

Kurnaz E., Kartal Baykan E., Türkyılmaz A., Yaralı O., Yavaş Abalı Z., Turan S., et al.

Hormone research in paediatrics , cilt.93, sa.9-10, ss.558-566, 2020 (SCI-Expanded, Scopus)

99. 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 , cilt.35, sa.1, ss.79-82, 2020 (SCI-Expanded, Scopus)

100. Adrenocortical carcinoma in atypical Beckwith-Wiedemann syndrome due to loss of methylation at imprinting control region 2

Eltan M., Arslan A., Cerit K., Menevse T., Kaygusuz S., Eker N., et al.

PEDIATRIC BLOOD & CANCER , cilt.67, sa.1, 2020 (SCI-Expanded, Scopus)

101. Letter to the Editor: Dysosteosclerosis related to the unique mutation in SLC29A3

Turan S.

Bone , cilt.128, 2019 (SCI-Expanded)

102. Characteristics of Turkish children with Type 2 diabetes at onset: a multicentre, cross-sectional study.

Hatun S., Yesiltepe Mutlu G., Cinaz P., Turan S., Ekberzade A., Bereket A., et al.

Diabetic medicine : a journal of the British Diabetic Association , cilt.36, sa.10, ss.1243-1250, 2019 (SCI-Expanded) Sürdürülebilir Kalkınma

103. A Real-Life Experience with A New Insulin Co-Formulation Degludec/Aspart For One Year In Poorly Controlled Children And Adolescents With Type 1 Diabetes

Kırkgöz T., Eltan M., Kaygusuz S. B., Abali Z. Y., Güran T., Bereket A., et al.

HORMONE RESEARCH IN PAEDIATRICS , cilt.91, ss.534-535, 2019 (SCI-Expanded) Sürdürülebilir Kalkınma

104. 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 , cilt.91, ss.329-330, 2019 (SCI-Expanded)

105. 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 , cilt.91, ss.589, 2019 (SCI-Expanded)

106. Characteristics of puberty, pubertal height gain and final height in children with classical 21 hydroxylase deficiency

Abali Z. Y., Yildiz M., Bas F., Onal H., Abalı S., Cilsaat G., et al.

HORMONE RESEARCH IN PAEDIATRICS , cilt.91, ss.205-206, 2019 (SCI-Expanded)

107. Age of obesity onset could be the first indicator of future metabolic complications - preliminary data of prospective multicenter study

Gawlik A., Wasniewska M., BEREKET A., Antosz A., Aversa T., Corica D., et al.

HORMONE RESEARCH IN PAEDIATRICS , cilt.91, ss.153-154, 2019 (SCI-Expanded) Sürdürülebilir Kalkınma

108. Cushing Syndrome due to an adrenacortical carcinoma in a baby with atypical Beckwith-Wiedemann Syndrome

Eltan M., Cerit K., Kaygusuz S. B., Ates E., Eker N., Bagci P., et al.

HORMONE RESEARCH IN PAEDIATRICS , cilt.91, ss.371, 2019 (SCI-Expanded)

109. 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 , cilt.91, ss.128, 2019 (SCI-Expanded)

110. How to Approach Systemic Hypersensitivity reactions to Gonadotropin Releasing Hormone Analogues during treatment of Central Precocious Puberty

KIRKGÖZ T., Karakoc E., Kiykim A., Bugrul F., Helvacioglu D., Eltan S. B., et al.

HORMONE RESEARCH IN PAEDIATRICS , cilt.91, ss.185, 2019 (SCI-Expanded)

111. Genotype and Phenotype Characterization of Turkish Patients with Vitamin D Dependent Rickets Type IA

Kaygusuz S. B., Ata P., Kırkgöz T., Abali Z. Y., Eltan M., Tosun B. G., et al.

HORMONE RESEARCH IN PAEDIATRICS , cilt.91, ss.215, 2019 (SCI-Expanded)

112. Hypergonadotropic hypogonadism in 46, XX adolescents without gonadotoxic therapy: Clinical features and molecular etiologies

Abali Z. Y., Jolly A., GÜRAN T., Bayram Y., ABALI S., Bas S., et al.

HORMONE RESEARCH IN PAEDIATRICS , cilt.91, ss.265, 2019 (SCI-Expanded)

113. 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 , cilt.91, ss.384, 2019 (SCI-Expanded)

114. Evaluation of molecular characteristics and steroid metabolomics in a large cohort of children with 3 beta-hydroxysteroid dehydrogenase 2 deficiency

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

HORMONE RESEARCH IN PAEDIATRICS , cilt.91, ss.207, 2019 (SCI-Expanded)

115. 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 , cilt.91, ss.214, 2019 (SCI-Expanded)

116. Liraglutide in children and adolescents with type 2 diabetes

Tamborlane W. V., Barrientos-Pérez M., Fainberg U., Frimer-Larsen H., Hafez M., Hale P. M., et al.

New England Journal of Medicine , cilt.381, sa.7, ss.637-646, 2019 (SCI-Expanded, Scopus) Sürdürülebilir Kalkınma

117. 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., et al.

The Journal of clinical endocrinology and metabolism , cilt.104, sa.8, ss.3049-3067, 2019 (SCI-Expanded, Scopus)

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

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

HORMONES-INTERNATIONAL JOURNAL OF ENDOCRINOLOGY AND METABOLISM , cilt.18, sa.2, ss.229-236, 2019 (SCI-Expanded, Scopus)

119. Ptosis as a unique hallmark for autosomal recessive WNT1-associated osteogenesis imperfecta

Nampoothiri S., Guillemyn B., Elcioglu N., Jagadeesh S., Yesodharan D., Suresh B., et al.

AMERICAN JOURNAL OF MEDICAL GENETICS PART A , cilt.179, sa.6, ss.908-914, 2019 (SCI-Expanded, Scopus)

120. 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 , cilt.11, sa.2, ss.149-156, 2019 (SCI-Expanded, Scopus, TRDizin) Sürdürülebilir Kalkınma

121. 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 , cilt.180, sa.5, ss.291-309, 2019 (SCI-Expanded, Scopus)

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

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

JOURNAL OF CLINICAL RESEARCH IN PEDIATRIC ENDOCRINOLOGY , cilt.10, sa.4, ss.336-342, 2018 (SCI-Expanded, Scopus, TRDizin) Sürdürülebilir Kalkınma

123. THE CO-EXISTENCE OF TWO RARE DISEASES: A CASE REPORT

Saki M., KIRKGÖZ T., GÖKCE İ., Cicek N., ATA P., Turan S., et al.

PEDIATRIC NEPHROLOGY , cilt.33, sa.10, ss.1881, 2018 (SCI-Expanded, Scopus)

124. Diagnosis and management of pseudohypoparathyroidism and related disorders: First international Consensus Statement

Mantovani G., Bastepe M., Monk D., De Sanctis L., Thiele S., Usardi A., et al.

Nature Reviews Endocrinology , cilt.14, sa.8, ss.476-500, 2018 (SCI-Expanded, Scopus)

125. Biallelic and monoallelic ESR2 variants associated with 46,XY disorders of sex development

Baetens D., Güran T., Mendonca B. B., Gomes N. L., De Cauwer L., Peelman F., et al.

GENETICS IN MEDICINE , cilt.20, sa.7, ss.717-727, 2018 (SCI-Expanded, Scopus)

126. 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 , cilt.27, sa.11, ss.1913-1926, 2018 (SCI-Expanded, Scopus)

127. 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 , cilt.10, sa.2, ss.125-130, 2018 (SCI-Expanded, Scopus, TRDizin) Sürdürülebilir Kalkınma

128. Acquired modification of sphingosine-1-phosphate lyase activity is not related to adrenal insufficiency

Sünter G., Enver E. O., Akbarzade A., Turan S., Vatansever P., Günal D., et al.

BMC NEUROLOGY , cilt.18, 2018 (SCI-Expanded)

129. Recurrent Hypoglycemia in a Preschooler Girl with Overgrowth: Isolated ACTH-Deficiency with a Novel TPIT Mutation

Abali Z. Y., Yesil G., Kırkgöz T., Kaygusuz S. B., Turan S., Bereket A., et al.

HORMONE RESEARCH IN PAEDIATRICS , cilt.90, ss.132, 2018 (SCI-Expanded)

130. 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 , cilt.90, ss.166-167, 2018 (SCI-Expanded)

131. An 18 Month Old Boy with Hypoglycemic Convulsion and Obesity Due to POMC Deficiency

Kaygusuz S. B., Yesil G., Kırkgöz T., Turan S., Bereket A., Güran T.

HORMONE RESEARCH IN PAEDIATRICS , cilt.90, ss.514, 2018 (SCI-Expanded) Sürdürülebilir Kalkınma

132. Nationwide Hypophosphatemic Rickets Study

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

HORMONE RESEARCH IN PAEDIATRICS , cilt.90, ss.109-110, 2018 (SCI-Expanded)

133. Persistent Mullerian duct syndrome: Rare But Important Aetiology of an Inguinal Hernia and Cryptorchidism in Boys

Bereket A., Bugrul F., Kırkgöz T., Karadeniz Cerit K., Canmemiş A., Turan S., et al.

HORMONE RESEARCH IN PAEDIATRICS , cilt.90, ss.568, 2018 (SCI-Expanded)

134. Diagnosis and Management of Pseudohypoparathyroidism and Related Disorders: First International Consensus Statement

Mantovani G., Bastepe M., Monk D., de Sanctis L., Thiele S., Usardi A., et al.

HORMONE RESEARCH IN PAEDIATRICS , cilt.90, ss.108-109, 2018 (SCI-Expanded)

135. An Unusual Cause of Short Stature

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

HORMONE RESEARCH IN PAEDIATRICS , cilt.90, ss.184-185, 2018 (SCI-Expanded)

136. 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 , cilt.90, ss.597, 2018 (SCI-Expanded)

137. Current Nomenclature of Pseudohypoparathyroidism: Inactivating Parathyroid Hormone/Parathyroid Hormone-Related Protein Signaling Disorder

Turan S.

JOURNAL OF CLINICAL RESEARCH IN PEDIATRIC ENDOCRINOLOGY , cilt.9, ss.58-68, 2017 (SCI-Expanded, Scopus, TRDizin)

138. 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 , cilt.18, sa.7, ss.607-613, 2017 (SCI-Expanded)

139. 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 , cilt.30, sa.4, ss.449-455, 2017 (SCI-Expanded, Scopus)

140. Heterotrimeric G proteins in the control of parathyroid hormone actions

Bastepe M., Turan S., He Q.

JOURNAL OF MOLECULAR ENDOCRINOLOGY , cilt.58, sa.4, 2017 (SCI-Expanded, Scopus) Sürdürülebilir Kalkınma

141. Pycnodysostosis at otorhinolaryngology

Baglam T., BİNNETOĞLU A., Topuz M. F., Ikizoglu N. B., Ersu R., Turan S., et al.

INTERNATIONAL JOURNAL OF PEDIATRIC OTORHINOLARYNGOLOGY , cilt.95, ss.91-96, 2017 (SCI-Expanded, Scopus)

142. Persistent hyperglycemia in a neonate: Is it a complication of therapeutic hypothermia?

Ozdemir H., MEMİŞOĞLU A., Alp-Unkar Z., Arcagok B., Bilgen H. S., Turan S., et al.

TURKISH JOURNAL OF PEDIATRICS , cilt.59, sa.2, ss.193-196, 2017 (SCI-Expanded)

143. CLINICAL CHARACTERISTICS OF TURKISH CHILDREN AND ADOLESCENTS WITH TYPE 2 DIABETES

Hatun S., Mutlu G. Y., CİNAZ P., Erbas M. Y., Akcay T., Onal H., et al.

HORMONE RESEARCH IN PAEDIATRICS , cilt.88, ss.282, 2017 (SCI-Expanded) Sürdürülebilir Kalkınma

144. 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 , cilt.88, ss.54, 2017 (SCI-Expanded)

145. SIMULTANEOUS PROFILING OF 17 STEROID HORMONES USING LIQUID CHROMATOGRAPHY TANDEM MASS SPECTROMETRY IN NEWBORN AND EARLY INFANCY

Enver E. O., Vatansever P., Guran O., Bilgin L., Boran P., Turan S., et al.

HORMONE RESEARCH IN PAEDIATRICS , cilt.88, ss.51, 2017 (SCI-Expanded)

146. The diagnostic value of soluble urokinase plasminogen activator receptor (suPAR) compared to C-reactive protein (CRP) and procalcitonin (PCT) in children with systemic inflammatory response syndrome (SIRS)

Sirinoglu M., Soysal A., Karaaslan A., KEPENEKLİ KADAYİFCİ E., Yalindag-Ozturk N., Cinel I., et al.

JOURNAL OF INFECTION AND CHEMOTHERAPY , cilt.23, sa.1, ss.17-22, 2017 (SCI-Expanded, Scopus)

147. CLINICAL AND LABORATORY CHARACTERISTICS OF HYPERPROLACTINEMIC CHILDREN AND ADOLESCENTS: NATIONAL SURVEY

EREN E., Ergur A. T., İŞGÜVEN Ş. P., Bitkin E. C., BERBEROĞLU M., ŞIKLAR Z., et al.

HORMONE RESEARCH IN PAEDIATRICS , cilt.88, ss.313-314, 2017 (SCI-Expanded) Sürdürülebilir Kalkınma

148. From pseudohypoparathyroidism to inactivating PTH/PTHrP signalling disorder (iPPSD), a novel classification proposed by the EuroPHP network

Thiele S., Mantovani G., Barlier A., Boldrin V., Bordogna P., De Sanctis L., et al.

EUROPEAN JOURNAL OF ENDOCRINOLOGY , cilt.175, sa.6, 2016 (SCI-Expanded)

149. 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 , cilt.11, sa.5, ss.383-8, 2016 (SCI-Expanded, Scopus) Sürdürülebilir Kalkınma

150. GCK gene mutations are a common cause of childhood-onset MODY (maturity-onset diabetes of the young) in Turkey.

Haliloglu B., Hysenaj G., Atay Z., GÜRAN T., Abali S., Turan S., et al.

Clinical endocrinology , cilt.85, sa.3, ss.393-9, 2016 (SCI-Expanded) Sürdürülebilir Kalkınma

151. The Growth Characteristics of Patients with Noonan Syndrome: Results of Three Years of Growth Hormone Treatment: A Nationwide Multicenter Study

ŞIKLAR Z., Genens M., Poyrazoglu S., Bas F., Darendeliler F., Bundak R., et al.

JOURNAL OF CLINICAL RESEARCH IN PEDIATRIC ENDOCRINOLOGY , cilt.8, sa.3, ss.305-312, 2016 (SCI-Expanded, Scopus, TRDizin)

152. 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 , cilt.8, ss.14, 2016 (SCI-Expanded)

153. Cathepsin K osteoporosis trials, pycnodysostosis and mouse deficiency models: Commonalities and differences

Broemme D., Panwar P., Turan S.

EXPERT OPINION ON DRUG DISCOVERY , cilt.11, sa.5, ss.457-472, 2016 (SCI-Expanded, Scopus)

154. 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 , cilt.101, sa.5, ss.1980-1988, 2016 (SCI-Expanded, Scopus)

155. The diagnostic value of soluble urokinase plasminogen activator receptor compared with C-reactive protein and procalcitonin in children with febrile neutropenia

Sirinoglu M., Soysal A., Karaaslan A., KEPENEKLİ KADAYİFCİ E., Cinel I., KOÇ A., et al.

Pediatric Hematology and Oncology , cilt.33, sa.3, ss.200-208, 2016 (SCI-Expanded)

156. Anthropometric findings from birth to adulthood and their relation with karyotpye distribution in Turkish girls with Turner syndrome

Sari E., BEREKET A., Yesilkaya E., Bas F., Bundak R., Aydin B. K., et al.

AMERICAN JOURNAL OF MEDICAL GENETICS PART A , cilt.170, sa.4, ss.942-948, 2016 (SCI-Expanded)

157. Thiamine Responsive Megaloblastic Anemia Due to SLCA19A2 Gene Mutation: Another Cause of Neonatal Diabetes with Succcesfull Switch from Insulin to Thiamine

Bas S., Akbarzade A., Atay Z., Gurbanov Z., GÜRAN T., Turan S., et al.

HORMONE RESEARCH IN PAEDIATRICS , cilt.86, ss.244, 2016 (SCI-Expanded) Sürdürülebilir Kalkınma

158. From Pseudohypoparathyroidism to Inactivating PTH/PTHrP Signaling Disorder (iPPSD), a Novel Classification Proposed by the European EuroPHP-Network

Thiele S., Mantovani G., Barlier A., Bordogna P., Elli F. M., Freson K., et al.

HORMONE RESEARCH IN PAEDIATRICS , cilt.86, ss.31, 2016 (SCI-Expanded)

159. Nonsense Mutation in SPARC Gene Causing Autosomal Recessive Ostegenesis Imperfecta

Abali S., Arman A., Atay Z., Bas S., Cam S., Gormez Z., et al.

HORMONE RESEARCH IN PAEDIATRICS , cilt.86, ss.167, 2016 (SCI-Expanded)

160. 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 , cilt.86, ss.451, 2016 (SCI-Expanded)

161. 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 , cilt.86, ss.457-458, 2016 (SCI-Expanded)

162. beta-hCG from an Occult Source Causing Peripheral Precocious Puberty: Identification of the Tumour 6 Years After Presentation

Ekberzade A., Abali S., Atay Z., Bas S., Gurbanov Z., Turan S., et al.

HORMONE RESEARCH IN PAEDIATRICS , cilt.86, ss.428, 2016 (SCI-Expanded)

163. 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 , cilt.86, ss.175-176, 2016 (SCI-Expanded)

164. 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 , cilt.101, sa.1, ss.283-291, 2016 (SCI-Expanded, Scopus)

165. The Effect of Subclinical Hypothyroidism (SH) and Treatment of SH with L-T4 on Basal Metabolic Rate in Obese Children: A Prospective Study

Muzafferova N., Bas S., Atay Z., Bereket A., Turan S.

HORMONE RESEARCH IN PAEDIATRICS , cilt.86, ss.303, 2016 (SCI-Expanded)

166. H syndrome: a multifaceted histiocytic disorder with hyperpigmentation and hypertrichosis.

Tekin B., Atay Z., Ergun T., Can M., TÜNEY D., Babay S., et al.

Acta dermato-venereologica , cilt.95, sa.8, ss.1021-3, 2015 (SCI-Expanded)

167. Growth curves for Turkish Girls with Turner Syndrome: Results of the Turkish Turner Syndrome Study Group

Darendeliler F., Yesilkaya E., BEREKET A., Bas F., Bundak R., Sari E., et al.

JOURNAL OF CLINICAL RESEARCH IN PEDIATRIC ENDOCRINOLOGY , cilt.7, sa.3, ss.183-191, 2015 (SCI-Expanded)

168. Effects of leukemia inhibitory receptor gene mutations on human hypothalamo-pituitary-adrenal function.

Guran T., Guran O., Paketci C., Kipoglu O., Firat I., Turan S., et al.

Pituitary , cilt.18, sa.4, ss.456-60, 2015 (SCI-Expanded) Sürdürülebilir Kalkınma

169. Higher insulin detemir doses are required for the similar glycemic control: comparison of insulin detemir and glargine in children with type 1 diabetes mellitus.

Abali S., Turan S., Atay Z., GÜRAN T., Haliloglu B., BEREKET A.

Pediatric diabetes , cilt.16, sa.5, ss.361-6, 2015 (SCI-Expanded) Sürdürülebilir Kalkınma

170. GNAS Spectrum of Disorders

Turan S., Bastepe M.

CURRENT OSTEOPOROSIS REPORTS , cilt.13, sa.3, ss.146-158, 2015 (SCI-Expanded, Scopus) Sürdürülebilir Kalkınma

171. Normative Data of Thyroid Volume-Ultrasonographic Evaluation of 422 Subjects Aged 0-55 Years

Aydiner O., AYDINER E., Akpinar I., Turan S., BEREKET A.

JOURNAL OF CLINICAL RESEARCH IN PEDIATRIC ENDOCRINOLOGY , cilt.7, sa.2, ss.98-101, 2015 (SCI-Expanded, Scopus, TRDizin)

172. 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 , cilt.100, sa.5, 2015 (SCI-Expanded, Scopus)

173. European guidance for the molecular diagnosis of pseudohypoparathyroidism not caused by point genetic variants at GNAS: An EQA study

Garin I., Mantovani G., Aguirre U., Barlier A., Brix B., Elli F. M., et al.

European Journal of Human Genetics , cilt.23, sa.4, ss.438-444, 2015 (SCI-Expanded, Scopus)

174. Turner Syndrome and Associated Problems in Turkish Children: A Multicenter Study

Yesilkaya E., BEREKET A., Darendeliler F., Bas F., Poyrazoglu S., Aydin B. K., et al.

JOURNAL OF CLINICAL RESEARCH IN PEDIATRIC ENDOCRINOLOGY , cilt.7, sa.1, ss.27-36, 2015 (SCI-Expanded)

175. Current Practice in Diagnosis and Treatment of Growth Hormone Deficiency in Childhood: A Survey from Turkey

Poyrazoglu S., Akcay T., ARSLANOĞLU İ., ATABEK M. E., Atay Z., BERBEROĞLU M., et al.

JOURNAL OF CLINICAL RESEARCH IN PEDIATRIC ENDOCRINOLOGY , cilt.7, sa.1, ss.37-44, 2015 (SCI-Expanded) Sürdürülebilir Kalkınma

176. Evidence of hormone resistance in a pseudo-pseudohypoparathyroidism patient with a novel paternal mutation in GNAS.

Turan S., Thiele S., Tafaj O., Brix B., Atay Z., Abali S., et al.

Bone , cilt.71, ss.53-7, 2015 (SCI-Expanded)

177. Premature pubarche, hyperinsulinemia and hypothyroxinemia: novel manifestations of congenital portosystemic shunts (Abernethy malformation) in children.

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

Hormone research in paediatrics , cilt.83, sa.4, ss.282-7, 2015 (SCI-Expanded, Scopus)

178. CLINICAL AND CEPHALOMETRIC ANALYSIS OF THREE CASES WITH PYCNODYSOSTOSIS: CASE REPORTS

Capan E., Turan S., Kilicoglu H.

JOURNAL OF ISTANBUL UNIVERSITY FACULTY OF DENTISTRY , cilt.49, sa.1, ss.51-55, 2015 (ESCI)

179. Prevalence of acne in primary school children and the relationship of acne with pubertal maturation

Erdogan H. K., Altunay I. K., Turan S.

TURKDERM-ARCHIVES OF THE TURKISH DERMATOLOGY AND VENEROLOGY , cilt.48, sa.4, ss.182-186, 2014 (SCI-Expanded)

180. The Frequency and the Effects of 21-Hydroxylase Gene Defects in Congenital Adrenal Hyperplasia Patients

Kirac D., GÜNEY A. İ., Akcay T., GÜRAN T., ULUCAN K., Turan S., et al.

ANNALS OF HUMAN GENETICS , cilt.78, sa.6, ss.399-409, 2014 (SCI-Expanded)

181. Does common channel length affect surgical choice in female congenital adrenal hyperplasia patients?

Tugtepe H., Thomas D. T., Turan S., Cizmecioglu F., Hatun S., BEREKET A., et al.

JOURNAL OF PEDIATRIC UROLOGY , cilt.10, sa.5, ss.948-954, 2014 (SCI-Expanded)

182. Sleep disordered breathing in children with endocrinological problems

Gokdemir Y., Aksu H. E., Erdem E., Lkizoglu N. B., Karakoc F., Karadag B. T., et al.

EUROPEAN RESPIRATORY JOURNAL , cilt.44, 2014 (SCI-Expanded)

183. Hypoglycemia: An unrecognized problem m cystic fibrosis (CF) patients unmasked by continues glucose monitorisation (CGM)

Haliloglu B., Gokdemir Y., Atay Z., Abali S., Guran T., Karakoc F., et al.

EUROPEAN RESPIRATORY JOURNAL , cilt.44, 2014 (SCI-Expanded)

184. Sleep disordered breathing in pycnodysostosis patients

Lkizoglu N. B., Gokdemir Y., Turan S., Atay Z., Haliloglu B., Karakoc F., et al.

EUROPEAN RESPIRATORY JOURNAL , cilt.44, 2014 (SCI-Expanded)

185. Current research on pycnodysostosis.

Turan S.

Intractable & rare diseases research , cilt.3, sa.3, ss.91-3, 2014 (SCI-Expanded)

186. AR and SRD5A2 gene mutations in a series of 51 Turkish 46,XY DSD children with a clinical diagnosis of androgen insensitivity

Akcay T., Fernandez-Cancio M., Turan S., Gueran T., Audi L., Bereket A.

ANDROLOGY , cilt.2, sa.4, ss.572-578, 2014 (SCI-Expanded, Scopus)

187. Novel homozygous inactivating mutation of the calcium-sensing receptor gene (CASR) in neonatal severe hyperparathyroidism-lack of effect of cinacalcet.

Atay Z., BEREKET A., Haliloglu B., Abali S., Ozdogan T., Altuncu E., et al.

Bone , cilt.64, ss.102-7, 2014 (SCI-Expanded, Scopus) Sürdürülebilir Kalkınma

188. The frequency and the effects of 21 Hydroxylase gene defects in congenital adrenal hyperplasial patients

KIRAÇ D., GÜNEY A. İ., Akçay T., Güran t., ULUCAN K., TURAN S., et al.

Annals Of Human Genetics , 2014 (SCI-Expanded, Scopus)

189. Cathepsin K analysis in a pycnodysostosis cohort: demographic, genotypic and phenotypic features

Arman A., Bereket A., Çoker A., Şimşek Kiper P. Ö., Güran T., Özkan B., et al.

ORPHANET JOURNAL OF RARE DISEASES , cilt.9, 2014 (SCI-Expanded)

190. Postnatal Establishment of Allelic Gas Silencing as a Plausible Explanation for Delayed Onset of Parathyroid Hormone Resistance Owing to Heterozygous Gas Disruption

Turan S., Fernandez-Rebollo E., Aydin C., Zoto T., Reyes M., Bounoutas G., et al.

JOURNAL OF BONE AND MINERAL RESEARCH , cilt.29, sa.3, ss.749-760, 2014 (SCI-Expanded, Scopus)

191. Identification of PENDRIN (SLC26A4) Mutations in Patients With Congenital Hypothyroidism and "Apparent" Thyroid Dysgenesis

Kuehnen P., Turan S., Froehler S., Gueran T., Abali S., Biebermann H., et al.

JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM , cilt.99, sa.1, 2014 (SCI-Expanded, Scopus)

192. Evaluation of bone metabolism in patients receiving home ventilation

Gökdemir Y., Erdem Eralp E., Şen V., Karakoc F., Ersu R., Turan S., et al.

EUROPEAN RESPIRATORY JOURNAL , cilt.42, 2013 (SCI-Expanded)

193. 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 , cilt.172, sa.6, ss.851-3, 2013 (SCI-Expanded)

194. A novel homozygous TMEM70 mutation results in congenital cataract and neonatal mitochondrial encephalo-cardiomyopathy.

Atay Z., BEREKET A., Turan S., Haliloglu B., MEMİŞOĞLU A., Khayat M., et al.

Gene , cilt.515, sa.1, ss.197-9, 2013 (SCI-Expanded)

195. The GNAS Complex Locus and Human Diseases Associated with Loss-of-Function Mutations or Epimutations within This Imprinted Gene

Turan S., Bastepe M.

HORMONE RESEARCH IN PAEDIATRICS , cilt.80, sa.4, ss.229-241, 2013 (SCI-Expanded, Scopus) Sürdürülebilir Kalkınma

196. Maternal Thyroid Dysfunction and Neonatal Thyroid Problems

Ozdemir H., Akman I., Coskun S., Demirel U., Turan S., BEREKET A., et al.

INTERNATIONAL JOURNAL OF ENDOCRINOLOGY , cilt.2013, 2013 (SCI-Expanded) Sürdürülebilir Kalkınma

197. De Novo STX16 Deletions: An Infrequent Cause of Pseudohypoparathyroidism Type Ib that Should Be Excluded in Sporadic Cases

Turan S., Ignatius J., Moilanen J. S., Kuismin O., Stewart H., Mann N. P., et al.

JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM , cilt.97, sa.12, 2012 (SCI-Expanded)

198. An atypical case of familial glucocorticoid deficiency without pigmentation caused by coexistent homozygous mutations in MC2R (T152K) and MC1R (R160W).

Turan S., Hughes C., Atay Z., GÜRAN T., Haliloglu B., Clark A. J. L., et al.

The Journal of clinical endocrinology and metabolism , cilt.97, sa.5, 2012 (SCI-Expanded)

199. Loss of XL alpha s (extra-large alpha s) imprinting results in early postnatal hypoglycemia and lethality in a mouse model of pseudohypoparathyroidism Ib

Fernandez-Rebollo E., Maeda A., Reyes M., Turan S., Froehlich L. F., Plagge A., et al.

PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA , cilt.109, sa.17, ss.6638-6643, 2012 (SCI-Expanded, Scopus) Sürdürülebilir Kalkınma

200. Clinical and molecular characterization of Turkish patients with familial hypomagnesaemia: novel mutations in TRPM6 and CLDN16 genes

GÜRAN T., Akcay T., BEREKET A., Atay Z., Turan S., Haisch L., et al.

NEPHROLOGY DIALYSIS TRANSPLANTATION , cilt.27, sa.2, ss.667-673, 2012 (SCI-Expanded, Scopus)

201. The prevalence and risk factors of premature thelarche and pubarche in 4-to 8-year-old girls

Atay Z., Turan S., GÜRAN T., FURMAN A., BEREKET A.

ACTA PAEDIATRICA , cilt.101, sa.2, 2012 (SCI-Expanded)

202. 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 , cilt.166, sa.1, ss.43-48, 2012 (SCI-Expanded, Scopus)

203. The Exon 3-Deleted/Full-Length Growth Hormone Receptor Polymorphism and Response to Growth Hormone Therapy in Growth Hormone Deficiency and Turner Syndrome: A Multicenter Study

Bas F., Darendeliler F., Aycan Z., Cetinkaya E., BERBEROĞLU M., ŞIKLAR Z., et al.

HORMONE RESEARCH IN PAEDIATRICS , cilt.77, sa.2, ss.85-93, 2012 (SCI-Expanded)

204. Extra-long G alpha s Variant XL alpha s Protein Escapes Activation-induced Subcellular Redistribution and Is Able to Provide Sustained Signaling

Liu Z., Turan S., Wehbi V. L., Vilardaga J., Bastepe M.

JOURNAL OF BIOLOGICAL CHEMISTRY , cilt.286, sa.44, ss.38558-38569, 2011 (SCI-Expanded, Scopus) Sürdürülebilir Kalkınma

205. Prevalence of type 1 diabetes mellitus in 6-18-yr-old school children living in Istanbul, Turkey

Akesen E., Turan S., Güran T., Atay Z., Save D., Bereket A.

PEDIATRIC DIABETES , cilt.12, sa.6, ss.567-571, 2011 (SCI-Expanded) Sürdürülebilir Kalkınma

206. Exclusion of the GNAS locus in PHP-Ib patients with broad GNAS methylation changes: Evidence for an autosomal recessive form of PHP-Ib?

Fernández-Rebollo E., Pérez De Nanclares G., Lecumberri B., Turan S., Anda E., Pérez-Nanclares G., et al.

Journal of Bone and Mineral Research , cilt.26, sa.8, ss.1854-1863, 2011 (SCI-Expanded)

207. Puberty and Influencing Factors in Schoolgirls Living in Istanbul: End of the Secular Trend?

Atay Z., Turan S., GÜRAN T., FURMAN A., BEREKET A.

PEDIATRICS , cilt.128, sa.1, 2011 (SCI-Expanded)

208. 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 , cilt.3, ss.7-11, 2011 (SCI-Expanded, Scopus)

209. 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 , cilt.24, sa.1, ss.7-12, 2011 (SCI-Expanded)

210. Radiologic and hormonal evaluation of pituitary abnormalities in patients with Bardet-Biedl syndrome

Guran T., Ekinci G., Atay Z., Turan S., Akcay T., Bereket A.

CLINICAL DYSMORPHOLOGY , cilt.20, sa.1, ss.26-31, 2011 (SCI-Expanded, Scopus)

211. Recessive versus imprinted disorder: consanguinity can impede establishing the diagnosis of autosomal dominant pseudohypoparathyroidism type Ib

Turan S., Akin L., Akcay T., Adal E., Sarikaya S., Bastepe M., et al.

EUROPEAN JOURNAL OF ENDOCRINOLOGY , cilt.163, sa.3, ss.489-493, 2010 (SCI-Expanded)

212. A mutation in thyroid hormone receptor beta causing "resistance to thyroid hormone" in a neonate

Cömert S., Akin Y., Vitrinel A., Telatar B., Aǧikuru T., Gözü H., et al.

MINERVA PEDIATRICA , cilt.62, sa.4, ss.419-422, 2010 (SCI-Expanded)

213. Deletion of the Noncoding GNAS Antisense Transcript Causes Pseudohypoparathyroidism Type Ib and Biparental Defects of GNAS Methylation in cis

Chillambhi S., Turan S., Hwang D., Chen H., Jueppner H., Bastepe M.

JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM , cilt.95, sa.8, ss.3993-4002, 2010 (SCI-Expanded) Sürdürülebilir Kalkınma

214. 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 , cilt.46, ss.427-430, 2010 (SCI-Expanded)

215. Circulating insulin-like growth factor binding protein-4 (IGFBP-4) is not regulated by parathyroid hormone and vitamin D in vivo: Evidence from children with rickets

BEREKET A., Cesur Y., Özkan B., Adal E., Turan S., Onan S. H., et al.

JCRPE Journal of Clinical Research in Pediatric Endocrinology , cilt.2, sa.1, ss.17-20, 2010 (SCI-Expanded)

216. Identification of a novel dentin matrix protein-1 (DMP-1) mutation and dental anomalies in a kindred with autosomal recessive hypophosphatemia

Turan S., Aydin C., Bereket A., Akcay T., Gueran T., Yaralioglu B. A., et al.

BONE , cilt.46, sa.2, ss.402-409, 2010 (SCI-Expanded, Scopus)

217. T4 plus T3 Treatment in Children with Hypothyroidism and Inappropriately Elevated Thyroid-Stimulating Hormone despite Euthyroidism on T4 Treatment

Akcay T., Turan S., GÜRAN T., Unluguzel G., HAKLAR G., BEREKET A.

HORMONE RESEARCH IN PAEDIATRICS , cilt.73, sa.2, ss.108-114, 2010 (SCI-Expanded, Scopus)

218. Long-term clinical outcome and carrier phenotype in autosomal recessive hypophosphatemia caused by a novel DMP1 mutation

Mäkitie O., Pereira R. C., Kaitila I., Turan S., Bastepe M., Laine T., et al.

Journal of Bone and Mineral Research , cilt.25, sa.10, ss.2165-2174, 2010 (SCI-Expanded, Scopus)

219. 9 Years follow-up of a patient with pituitary form of resistance to thyroid hormones (PRTH): Comparison of two treatment periods of D-thyroxine and triiodothyroacetic acid (TRIAC)

GÜRAN T., Turan S., Bircan R., BEREKET A.

Journal of Pediatric Endocrinology and Metabolism , cilt.22, sa.10, ss.971-978, 2009 (SCI-Expanded, Scopus)

220. 9 Years Follow-up of a Patient with Pituitary Form of Resistance to Thyroid Hormones (PRTH): Comparison of Two Treatment Periods of D-Thyroxine and Triiodothyroacetic Acid (TRIAC)

GÜRAN T., Turan S., BİRCAN R., BEREKET A.

JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM , cilt.22, sa.10, ss.971-978, 2009 (SCI-Expanded)

221. The role of leptin, soluble leptin receptor, resistin, and insulin secretory dynamics in the pathogenesis of hypothalamic obesity in children

GÜRAN T., Turan S., BEREKET A., Akcay T., Unluguzel G., Bas F., et al.

EUROPEAN JOURNAL OF PEDIATRICS , cilt.168, sa.9, ss.1043-1048, 2009 (SCI-Expanded) Sürdürülebilir Kalkınma

222. Electrocardiographic findings and QT dispersion in children with chest pain Çocuklarda idiyopatik göǧüs aǧrisinda EKG bulgulari ve QT dispersiyonu

AKALIN F., Turan S.

Turk Pediatri Arsivi , cilt.44, sa.2, ss.53-56, 2009 (Scopus)

223. Electrocardiographic findings and QT dispersion in children with chest pain

AKALIN F., Turan S.

TURK PEDIATRI ARSIVI-TURKISH ARCHIVES OF PEDIATRICS , cilt.44, sa.2, ss.53-56, 2009 (SCI-Expanded)

224. 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 , cilt.22, sa.4, ss.363-368, 2009 (SCI-Expanded)

225. Puberty in a case with novel 17-hydroxylase mutation and the putative role of estrogen in development of pubic hair

Truan S., Bereket A., Güran T., Akcay T., Papari-Zareei M., Auchus R. J.

EUROPEAN JOURNAL OF ENDOCRINOLOGY , cilt.160, sa.2, ss.325-330, 2009 (SCI-Expanded, Scopus)

226. 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 , cilt.72, ss.402, 2009 (SCI-Expanded)

227. 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 , cilt.22, sa.4, ss.363-368, 2009 (SCI-Expanded)

228. Final height in girls with idiopathic precocious puberty treated with leuprolide: dose-titration approach

Balanli E., GÜRAN T., Turan S., Atay Z., BEREKET A.

HORMONE RESEARCH , cilt.72, ss.123, 2009 (SCI-Expanded)

229. 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 , cilt.94, sa.10, ss.3633-3639, 2009 (SCI-Expanded, Scopus)

230. Alopecia: Association with resistance to thyroid hormones

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

Journal of Pediatric Endocrinology and Metabolism , cilt.22, sa.11, ss.1075-1081, 2009 (SCI-Expanded)

231. Adult height in Turkish patients with Turner syndrome without growth hormone treatment

BEREKET A., Turan S., Elcioglu N., Hacihanefioglu S., Memioglu N., Bas F., et al.

TURKISH JOURNAL OF PEDIATRICS , cilt.50, sa.5, ss.415-417, 2008 (SCI-Expanded)

232. Adult height in Turkish patients with Turner syndrome without growth hormone treatment.

Bereket A., Turan S., Elçioǧlu N., Hacihanefioǧlu S., Memioǧlu N., Baş F., et al.

The Turkish journal of pediatrics , cilt.50, sa.5, ss.415-7, 2008 (SCI-Expanded)

233. 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 , cilt.21, sa.8, ss.745-51, 2008 (SCI-Expanded)

234. Significance of acanthosis nigricans in childhood obesity

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

JOURNAL OF PAEDIATRICS AND CHILD HEALTH , cilt.44, sa.6, ss.338-341, 2008 (SCI-Expanded) Sürdürülebilir Kalkınma

235. Comparison of capillary blood ketone measurement by electrochemical method and urinary ketone in treatment of diabetic ketosis and ketoacidosis in children

Turan S., Omar A., Bereket A.

ACTA DIABETOLOGICA , cilt.45, sa.2, ss.83-85, 2008 (SCI-Expanded) Sürdürülebilir Kalkınma

236. Alendronate treatment in children with osteogenesis imperfecta

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

Indian Pediatrics , cilt.45, sa.2, ss.105-109, 2008 (SCI-Expanded, Scopus)

237. Identification of a novel dentin matrix protein-1 (DMP-1) mutation in a kindred with autosomal recessive hypophosphatemia and dental anomalies

Turan S., Bereket A., Aydin C., Akcay T., Gueran T., Yaralioglu B. A., et al.

HORMONE RESEARCH , cilt.70, ss.184-185, 2008 (SCI-Expanded)

238. 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 , cilt.1, sa.1, ss.43-8, 2008 (SCI-Expanded)

239. Alopecia areata: A new association with resistance to thyroid hormones in a family with novel TRb mutation

GÜRAN T., Bircan R., Akcay T., Turan S., BEREKET A.

HORMONE RESEARCH , cilt.70, ss.57, 2008 (SCI-Expanded)

240. 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 , cilt.75, sa.4, ss.432-436, 2008 (SCI-Expanded, Scopus)

241. Long-term follow-up of a patient with pituitary resistance to thyroid hormones: Comparison of D-thyroxine and triiodothyroacetic acid treatments

GÜRAN T., Bircan R., Turan S., Akcay T., BEREKET A.

HORMONE RESEARCH , cilt.70, ss.59-60, 2008 (SCI-Expanded)

242. Hypophosphatemic rickets: New and important roles for bone mineralization and phosphate homeostasis of Dentin matrix protein-1

Turan S., Bereket A., Guran T., Akcay T., Aydin C., Bastepe M., et al.

HORMONE RESEARCH , cilt.70, ss.14, 2008 (SCI-Expanded)

243. Polymorphisms in the vitamin D receptor gene in children with idiopathic hypercalcemia

Guney I., Turan S., Sevinc D., GÜRAN T., Akcay T., Karakoc E., et al.

HORMONE RESEARCH , cilt.70, ss.49, 2008 (SCI-Expanded)

244. Screening of Parents and Siblings of Patients with Thyroid Dysgenesis by Thyroid Function Tests and Ultrasound

Karakoc E., Turan S., Akpinar I., Isguven P., Adal E., Haklar G., et al.

HORMONE RESEARCH , cilt.70, sa.6, ss.329-339, 2008 (SCI-Expanded)

245. Familial thyroid dysgenesis: Which genes could be involved?

Castenet M., Carre A., BEREKET A., Guney I., AYDINER E., Turan S., et al.

HORMONE RESEARCH , cilt.70, ss.163, 2008 (SCI-Expanded)

246. 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 , cilt.70, ss.50, 2008 (SCI-Expanded)

247. A pilot for searching androgen receptor mutations in Turkish male pseudohermaphrodites with clinical diagnosis of androgen insensitivity syndrome

Akcay T., GÜRAN T., Turan S., Sevinc D., ULUCAN K., Guney I., et al.

HORMONE RESEARCH , cilt.70, ss.249, 2008 (SCI-Expanded)

248. Renal agenezisi olan bir Beckwith-Wiedemann Olgusu

Gökce İ., Göçmen İ., Bıyıklı N., Turan S., Alpay H.

TURKISH NEPHROLOGY, DIALYSIS AND TRANSPLANTATION JOURNAL , cilt.16, ss.196-197, 2007 (ESCI)

249. The effect of the mode of delivery on neonatal thyroid function.

Turan S., Bereket A., Angaji M., Koroglu O. A., Bilgen H. S., Onver T., et al.

The journal of maternal-fetal & neonatal medicine : the official journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians , cilt.20, sa.6, ss.473-6, 2007 (SCI-Expanded)

250. The effect of economic status on height, insulin-like growth factor (IGF)-I and IGF binding protein-3 concentrations in healthy Turkish children.

Turan S., Bereket A., Furman A., Omar A., Berber M., Ozen A., et al.

European journal of clinical nutrition , cilt.61, sa.6, ss.752-8, 2007 (SCI-Expanded)

251. Detection of Y chromosomal material in patients with a 45,X karyotype by PCR method

Semerci C. N., Satiroglu-Tufan N. L., Turan S., Bereket A., Tuysuz B., Yilmaz E., et al.

Tohoku Journal of Experimental Medicine , cilt.211, sa.3, ss.243-249, 2007 (SCI-Expanded)

252. A case of thyroid hormone resistance syndrome in a newborn

Gozu H., Bircan R., Comert S., Akin Y., Turan S., Seker M., et al.

HORMONE RESEARCH , cilt.68, ss.52, 2007 (SCI-Expanded)

253. Reference data for bone speed of sound measurement by quantitative ultrasound in healthy children

Omar A., Turan S., Bereket A.

Archives of Osteoporosis , cilt.1, ss.37-41, 2006 (SCI-Expanded)

254. Severe diabetic ketoacidosis: hyperventilation or relative hypoventilation

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

PEDIATRIC CRITICAL CARE MEDICINE , cilt.7, sa.3, ss.291, 2006 (SCI-Expanded) Sürdürülebilir Kalkınma

255. Serum IGF-I and IGFBP-3 levels of Turkish children during childhood and adolescence: Establishment of reference ranges with emphasis on puberty

Bereket A., Turan S., Omar A. O., Berber M.

Hormone Research , cilt.65, sa.2, ss.96-105, 2006 (SCI-Expanded)

256. Serum IGF-I and IGFBP-3 levels of Turkish children during childhood and adolescence: Establishment of reference ranges with emphasis on puberty

BEREKET A., TURAN S., Omar A., Berber M., ÖZEN A. O., Akbenlioglu C., et al.

Hormone Research , cilt.65, sa.2, ss.96-105, 2006 (SCI-Expanded, Scopus)

257. Factors related to childhood obesity

Bereket A., Turan S., Omar A., Berber M., Ozen A. O.

HORMONE RESEARCH , cilt.65, ss.82, 2006 (SCI-Expanded) Sürdürülebilir Kalkınma

258. Evaluation of patients with Graves' disease

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

HORMONE RESEARCH , cilt.65, ss.41, 2006 (SCI-Expanded)

259. Pycnodysostosis: A rare cause of short stature

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

HORMONE RESEARCH , cilt.65, ss.76, 2006 (SCI-Expanded)

260. 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 , cilt.65, ss.83, 2006 (SCI-Expanded) Sürdürülebilir Kalkınma

261. 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 , cilt.65, ss.86, 2006 (SCI-Expanded) Sürdürülebilir Kalkınma

262. Screening of parents and siblings of children with thyroid dysgenesis by thyroid function tests and ultrasound

Aydiner E., Turan S., Akpinar I., Isguven P., Adal E., Akcay T., et al.

HORMONE RESEARCH , cilt.65, ss.41, 2006 (SCI-Expanded)

263. Upper segment/lower segment ratio and armspan-height difference in healthy Turkish children

Turan S., Bereket A., Omar A., Berber M., Ozen A. O., Bekiroglu N.

ACTA PAEDIATRICA , cilt.94, sa.4, ss.407-413, 2005 (SCI-Expanded)

264. Effect of zinc supplementation on growth hormone secretion, IGF-I, IGFBP-3, somatomedin generation, alkaline phosphatase, osteocalcin and growth in prepubertal children with idiopathic short stature

Imamoǧlu S., BEREKET A., Turan S., Taga Y., HAKLAR G.

Journal of Pediatric Endocrinology and Metabolism , cilt.18, sa.1, ss.69-74, 2005 (SCI-Expanded)

265. Effect of zinc supplementation on growth hormone secretion, IGF-I, IGFBP-3, somatomedin generation, alkaline phosphatase, osteocalcin and growth in prepubertal children with idiopathic short stature

Imamoglu S., Bereket A., Turan S., Haklar G.

JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM , cilt.18, sa.1, ss.69-74, 2005 (SCI-Expanded)

266. Height, weight, IGF-I, IGFBP-3 and thyroid functions in prepubertal children with attention deficit hyperactivity disorder: effect of methylphenidate treatment.

Bereket A., Turan S., Karaman M., Haklar G., Ozbay F., Yazgan M.

Hormone research , cilt.63, sa.4, ss.159-64, 2005 (SCI-Expanded, Scopus)

267. A patient with hypopituitarism and isochromosome 18q mosaicism

Turan S., Saka N., Guney I., Bereket A.

HORMONE RESEARCH , cilt.64, sa.6, ss.261-265, 2005 (SCI-Expanded)

268. Addition of orlistat to conventional treatment in adolescents with severe obesity

Ozkan B., Bereket A., Turan S., Keskin S.

EUROPEAN JOURNAL OF PEDIATRICS , cilt.163, sa.12, ss.738-741, 2004 (SCI-Expanded) Sürdürülebilir Kalkınma

269. Increased QT dispersion in breath-holding spells

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

ACTA PAEDIATRICA , cilt.93, sa.6, ss.770-774, 2004 (SCI-Expanded, Scopus)

270. Two patients with Kabuki syndrome presenting with endocrine problems

Bereket A., Turan S., Alper G., Comu S., Alpay H., Akalin F.

JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM , cilt.14, sa.2, ss.215-220, 2001 (SCI-Expanded, Scopus)

271. Two patents with Kabuki Syndrome Presenting with endocrine problems

BEREKET A., TURAN S., ALPER G., COMU S., ALPAY H., AKALIN F.

Journal of Pediatric Endocrinology and Metabolism , sa.14, ss.215-220, 2001 (SCI-Expanded)

272. A case of glycogen storage disease type II with double aortic arch

Akalin F., Alper G., Oztunc F., Kotiloglu E., Turan S.

ACTA PAEDIATRICA , cilt.89, sa.7, ss.884-886, 2000 (SCI-Expanded)

273. Echocardiographic diagnosis of aortopulmonary window in a 4-day-old baby

AKALIN F., Oztunc F., TURAN S.

Marmara Medical Journal , cilt.12, sa.2, ss.98-100, 1999 (Scopus)

274. Etiological analysis of epilepsy during the infancy.

Alper G., Yilmaz Y., Turan S.

EPILEPSIA , cilt.40, ss.226, 1999 (SCI-Expanded)

Hakemli Bilimsel Toplantılarda Yayımlanmış Bildiriler 187

1. DISORDER OF ADRENAL EXCESS AND ADRENAL MEDULLA

Demircioğlu S.

EUROPEAN SOCİETY FOR PEDIATRIC ENDOCRINOLOGY WINTER SCHOOL, Cairo, Mısır, 23 Şubat - 01 Mart 2018, (Tam Metin Bildiri)

2. Identification of genetic etiology in 130 patients with congenital hypopituitarism

Abali Z., Toksoy G., BAŞ F., Guran T., Ozturk A., KARAMAN V., et al.

cilt.32, ss.1362-1363, (Özet Bildiri)

3. 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, Kıbrıs (Kktc), 23 - 27 Ekim 2024, ss.98, (Özet Bildiri)

4. Use of Vosoritide in Children with Achondroplasia Real Life Experince

Kahveci A., Helvacioglu D., Abali Z., Canbaz A., Gunay A., BEREKET A., et al.

cilt.97, ss.294, (Özet Bildiri)

5. **A rare cause of hypogonadotropic hypogonadism: KLB gene variant in a prepubertal boy evaluated for micropenis**

YAVAŞ ABALI Z., Yesilyurt A., DEMİRCİOĞLU S., Guran T., Haliloglu B., BEREKET A.

cilt.97, ss.301-302, (Özet Bildiri)

6. Clinical Characteristics and follow-up of Type 2 Diabetes in Children and Adolescents: A Single Center Experience

Gunes N., Helvacioglu D., Tosun B., Abali Z., Guran T., Haliloglu B., et al.

cilt.97, ss.365, (Özet Bildiri)

7. Basal Ganglia Calcification in Children with Hypoparathyroidism and Pseudohypoparathyroidism: Characterization of Relationships and Clinical and Laboratory Findings

Tosun B., Kurt I., Helvacioglu D., Abali Z., Guran T., BEREKET A., et al.

cilt.97, ss.479, (Özet Bildiri)

8. Polysomnography Findings and Respiratory Problems in Prader-Willi Syndrome: The Effect of Growth Hormone Treatment

Kelestemur E., Baysal E., Menevse T., Bas S., Kurt I., Kahveci A., et al.

cilt.97, ss.291, (Özet Bildiri)

9. Machine Learning-Based Decision Tree Model for the Diagnosis of Congenital Disorders of Adrenal Steroidogenesis Using LC-MS/MS-based Plasma Steroid Hormone Profiles

Erçetin A., Tosun B., Kirkgoz T., Abali Z., Eltan M., Akbarzade A., et al.

cilt.97, ss.101, (Özet Bildiri)

10. Thyroid Hormone Profile and Autoimmunity in Down Syndrome

Günay A., Helvacioglu D., Abali Z., Tosun B., Kahveci A., Kurt I., et al.

cilt.97, ss.466-467, (Özet Bildiri)

11. A real-world data analysis of 37 pediatric patients with pheochromocytoma and paraganglioma: Evaluation of the concordance between current diagnostic and treatment algorithms and clinical management practices in resource-limited settings

Kurt I., Tosun B., Uslu N., Kizilay D., Dikmen I., Comlek F., et al.

cilt.97, ss.475, (Özet Bildiri)

12. Genotype and phenotype characteristics and long-term follow-up of patients with Vitamin D Dependent Rickets Type II (VDDRII): A nationwide multicenter retrospective cross-sectional study

Cayir A., DEMİRCİOĞLU S., Eklioglu B., BAYRAMOĞLU E., Unal E., Yildiz M., et al.

cilt.97, ss.483-484, (Özet Bildiri)

13. CYP24A1 Mutations: Clinical and Laboratory Features in Patients Presenting with Hypercalcemia

Kurt I., Eltan M., Abali Z., Alavanda C., Demir S., ATA P., et al.

cilt.97, ss.92-93, (Özet Bildiri)

14. Final Height and Endocrine Complications in Children with Pilocytic Astrocytomas: A Retrospective Study

Canbaz A., Helvacioglu D., Tosun B., Abali Z., Sahin Y., Guran T., et al.

cilt.97, ss.97-98, (Özet Bildiri)

15. Nefrotik Sendrom ile başvuran H sendromu

Atalay A., Çiçek N., Gökce İ., Yılık E., Güven S., Türkkan Ö., et al.

12. Uluslararası Katılımlı Çocuk Nefroloji Kongresi, Ankara, Türkiye, 26 - 29 Ekim 2023, ss.128, (Özet Bildiri)

16. MUTATIONS IN SLC34A1/NPT2A AND SLC34A3/ NPT2C ARE ASSOCIATED WITH DISTINCT PHENOTYPES

Brunkhorst M., Brunkhorst L., Papizh S., Knebelmann B., DEMİRCİOĞLU S., Espinosa-Román L., et al.

cilt.38, (Özet Bildiri)

17. Juvenile Paget's Disease: Evaluation of Novel Mutation and Treatment Response

Kaygusuz S., Gokoglu M., DEMİRCİOĞLU S.

cilt.96, ss.172, (Özet Bildiri)

18. Long-Term Endocrine Complications of Medulloblastoma and The Effect of Growth Hormone Therapy on Final Height

Kelestemur E., Helvacioglu D., Tosun B., Kahveci A., Kurt I., Abali Z., et al.

cilt.96, ss.351, (Özet Bildiri)

19. Comparison of efficacy and safety of Leuprolide acetate depot 3.75 mg four-weekly versus 11.25 mg twelve-weekly in girls with central precocious puberty: A randomized-prospective study

Helvacioglu D., DEMİRCİOĞLU S., Güran T., Haliloglu B., Tosun B., Kahveci A., et al.

cilt.96, ss.592-593, (Özet Bildiri)

20. Exploring Childhood Hypoparathyroidism: Stepwise Genetic Evaluation Approach

Tosun B., Alavanda C., Kahveci A., Kurt I., Kelestemur E., Abali Z., et al.

cilt.96, ss.176-177, (Özet Bildiri)

21. Non-Osteogenesis Imperfecta Primary Osteoporosis in Children: Clinical and Genetic Features

Tosun B., Kaygusuz S., Alavanda C., Kahveci A., Kurt I., Kelestemur E., et al.

cilt.96, ss.159, (Özet Bildiri)

22. Validation of utility of a single LH measurement 40 minutes after depot Leuprolide acetate 3.75 mg and 11.25 mg in assessing gonadotropic activity in girls with CPP: Comparison with a standard GnRH stimulation test at diagnosis and during treatment

Helvacioglu D., DEMİRCİOĞLU S., Güran T., Haliloglu B., Turkmen N., Tosun B., et al.

cilt.96, ss.599, (Özet Bildiri)

23. An Obese HNF1β Case Presenting with Diabetic Ketoacidosis

Kahveci A., Kaplan G., ARSLAN ATEŞ E., Geckinli B., Guran T., DEMİRCİOĞLU S., et al.

cilt.96, ss.499, (Özet Bildiri)

24. Evaluation of Mitochondrial Bioenergetic Function in Mitochondrial and Type 1 Diabetes

Tosun B., Francisco A., Navarro C., Menevse T., Polat H., Hismi B., et al.

cilt.96, ss.181-182, (Özet Bildiri)

25. Admission Characteristics and Rates of Transient/Permanent Hypothyroidism in Infants from Congenital Hypothyroidism Screening

Kahveci A., Helvacioglu D., Kurt I., Kelestemur E., Tosun B., Abali Z., et al.

cilt.96, ss.570-571, (Özet Bildiri)

26. Clinical and molecular characteristics of 147 patients with primary congenital hypothyroidism: A single-center experience

Abali Z., Alavanda C., Eltan M., ARSLAN ATEŞ E., Helvacioglu D., Tosun B., et al.

cilt.96, ss.433, (Özet Bildiri)

27. Evaluation of two cases with 46,XX and 46,XY karyotypes diagnosed with 17a-hydroxylase deficiency

Kurt I., Sagsak E., Murat N., Tosun B., Helvacioglu D., Abali Z., et al.

cilt.96, ss.468, (Özet Bildiri)

28. Clinical and molecular genetic characteristics of 98 patients with congenital hypopituitarism: A single-center experience

Abali Z., ARSLAN ATEŞ E., Eltan M., DEMİRCİOĞLU S., BEREKET A., Guran T.

cilt.96, ss.72-73, (Özet Bildiri)

29. Single Gene Variations in Etiology in Children with Severe Obesity

Kahveci A., Kelestemur E., Kurt I., Guran T., DEMİRCİOĞLU S., BEREKET A., et al.

cilt.96, ss.224, (Özet Bildiri)

30. Physician and Family Awareness in the Diagnostic Process of Newly Diagnosed Type-1 Diabetes Mellitus

Kahveci A., Helvacioglu D., Kelestemur E., Kurt I., DEMİRCİOĞLU S., Guran T., et al.

cilt.96, ss.494, (Özet Bildiri)

31. Anthropometric, clinical, and molecular genetic characteristics of 42 patients with RASopathies

Abali Z., Geckinli B., Eltan M., Kahveci A., Tosun B., Helvacioglu D., et al.

cilt.96, ss.351, (Özet Bildiri)

32. A Novel Cause of Male Infertility and Hypergonadotropic Hypogonadism: Inhibin-A Deficiency Due to Loss of Function Variations of INHA

Ates E., Eltan M., ŞAHİN B., Tosun B., Menevse T., Geçkinli B., et al.

cilt.31, ss.352, (Özet Bildiri)

33. 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, İtalya, 15 - 17 Eylül 2022, (Özet Bildiri)

34. Osteogenezis İmperfekta’da Tedavi- Multidisipliner Yaklaşım Çocuk Endokrin Uzmanı Bakış Açısı

DEMİRCİOĞLU S.

25. Ulusal Pediatrik Endokrinoloji ve Diyabet Kongresi, 09 Ekim 2021, (Tam Metin Bildiri)

35. Bıldırcın Yumurtası Bir Endokrin Bozucu mudur?

Güran T., Surekli Karakus O., Turan S., Bereket A., Yegen B.

XXV. Ulusal Pediatrik Endokrinoloji & Diyabet Kongresi, Antalya, Türkiye, 6 - 10 Ekim 2021, ss.1-3, (Özet Bildiri)

36. İnsülin Degludek/Aspart ile Az Çoktur !

DEMİRCİOĞLU S.

25. Ulusal Pediatrik Endokrinoloji ve Diyabet Kongresi, 06 Ekim 2021, (Tam Metin Bildiri)

37. 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, Türkiye, 6 - 10 Ekim 2021, ss.1-3, (Tam Metin Bildiri)

38. 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, Türkiye, 06 Ekim 2021, (Tam Metin Bildiri)

39. 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 Ekim 2021, (Tam Metin Bildiri)

40. DNAJC3 Genindeki Bialelik Mutasyona Bağlı Hiperinsülinemik Hipoglisemi

Güran T., Gurpinar Tosun B., Turan S., Bereket A.

XXV. Ulusal Pediatrik Endokrinoloji & Diyabet Kongresi, Antalya, Türkiye, 6 - 10 Ekim 2021, ss.1-2, (Özet Bildiri)

41. 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, Türkiye, 6 - 10 Ekim 2021, ss.1-2, (Tam Metin Bildiri)

42. 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, Türkiye, 6 - 10 Ekim 2021, ss.1-2, (Tam Metin Bildiri)

43. 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, Türkiye, 6 - 10 Ekim 2021, ss.1-3, (Özet Bildiri)

44. Adrenocortical hormone profiles do not predict the molecular etiology in non-CAH primary adrenal insufficiency.

SEVEN MENEVŞE T., KENDİR DEMİRKOL Y., GÜRPINAR TOSUN B., BAYRAMOĞLU E., YILDIZ M., ACAR S., et al.

59th Annual Meeting of European Society of Pediatric Endocrinology, 22 - 25 Eylül 2021, (Özet Bildiri)

45. 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 Eylül 2021, (Özet Bildiri)

46. PARATİROİD HASTALIKLARI VE YÖNETİMİ

DEMİRCİOĞLU S.

VI. Pediatrik Endokrinoloji İleri Kursu, 11 Haziran 2021, (Tam Metin Bildiri)

47. Pediatrik hastalarda IDegAsp kullanımı ile ilgili esaslar nelerdir?

DEMİRCİOĞLU S.

42. Türkiye Endokrinoloji ve Metabolizma Hastalıkları Kongresi, 20 Mayıs 2021, (Tam Metin Bildiri)