Prof. Dr. Semra ÇETİNKAYA

1. In which cases of proximal hypospadias detailed investigations are necessary

Aydınbaş G., KARAMAN A., ÇETİNKAYA S., Karaman İ.

Pediatric Surgery International , cilt.42, sa.1, 2026 (SCI-Expanded, Scopus)

2. Changes in thyroid volume during the course of treatment of congenital primary hypothyroidism with an in situ thyroid gland

Yılmaz Y., ÇETİNKAYA S., MURATOĞLU ŞAHİN N.

Journal of Pediatric Endocrinology and Metabolism , cilt.39, sa.9, ss.875-882, 2026 (SCI-Expanded, Scopus)

3. Anorexia Nervosa Emerging after Swyer Syndrome Diagnosis

JCRPE Journal of Clinical Research in Pediatric Endocrinology , cilt.18, sa.3, ss.554-555, 2026 (SCI-Expanded, Scopus, TRDizin)

4. Atypical Biallelic Inheritance in “Dominant” Genes: Evidence From a Large-Scale Consanguineus Exome Cohort

Taşdelen E., Tekbaş U. C., Kolkıran A., ÇETİNKAYA S., KILIÇ M. K., Sezer A.

American Journal of Medical Genetics, Part A , cilt.200, sa.9, ss.2088-2098, 2026 (SCI-Expanded, Scopus)

5. A novel PAPSS2 pathogenic variant: expanding the mutational spectrum and genotype–phenotype landscape in skeletal dysplasia

Özdemir B. S., Lafcı N. G., Derinkuyu B. E., ÇETİNKAYA S., Şakar M., KESKİN M., et al.

Journal of Pediatric Endocrinology and Metabolism , cilt.39, sa.8, ss.819-827, 2026 (SCI-Expanded, Scopus)

6. Long-term clinical outcomes of primary adrenal insufficiency caused by homozygous CYP11A1 p.R451W variant

ÇAYIR A., DEMİRBİLEK H., Kurt I., Turkyilmaz A., Koca S. B., Ozbek M. N., et al.

European Journal of Endocrinology , cilt.195, sa.1, ss.35-42, 2026 (SCI-Expanded, Scopus)

7. Editorial: Advanced genomic techniques for congenital adrenal hyperplasia

ÇETİNKAYA S., Falhammar H.

Frontiers in Endocrinology , cilt.17, 2026 (SCI-Expanded, Scopus)

8. Genotype–Phenotype Spectrum of Non-Syndromic Monogenic Obesity in a National Paediatric Cohort

VELİOĞLU A., Karauzum S. U., Manyas H., Ozdemir B. S., ORBAK Z., Tercan U., et al.

Pediatric Obesity , cilt.21, sa.6, 2026 (SCI-Expanded, Scopus)

9. Meier-Gorlin syndrome due to a recurrent DONSON variant in a Turkish family: first report of thumb aplasia and long-term growth data

Sezer A., Yalçln F. Z., Kolklran A., ÇETİNKAYA S.

Journal of Pediatric Endocrinology and Metabolism , cilt.39, sa.4, ss.388-395, 2026 (SCI-Expanded, Scopus)

10. Management of Type 1 diabetes in adolescents: Effectiveness of the remote personalized system of instruction model

BORA GÜNEŞ N., Taşdelen Baş M., ÇETİNKAYA S., Yıldırım N.

Journal of Pediatric Nursing , cilt.87, ss.181-189, 2026 (SCI-Expanded, SSCI, Scopus)

11. Is the tracheal index useful for evaluating the thyroid in infants suspected of hypothyroidism?

MURATOĞLU ŞAHİN N., Cinar H. G., Sarikaya Ozdemir B., KESKİN M., ÇETİNKAYA S., SAVAŞ ERDEVE Ş.

Journal of Pediatric Endocrinology and Metabolism , cilt.39, sa.2, ss.143-149, 2026 (SCI-Expanded, Scopus)

12. What to Do for Atypia of Undetermined Significance in Pediatric Thyroid Nodules?

Uslu Z. Ö., Genel N., Küçükali E. T. T., Akın A., KARAMAN İ., ŞAHİN G., et al.

JCRPE Journal of Clinical Research in Pediatric Endocrinology , cilt.17, sa.4, ss.428-435, 2025 (SCI-Expanded, Scopus, TRDizin)

13. Central precocious puberty in boys; diagnosis, treatment and follow-up: a nation-wide study

Odabasi Gunes S., Sakar M., MURATOĞLU ŞAHİN N., KARAGÜZEL G., CİMBEK E. A., Darendeliler F., et al.

Endocrine , cilt.90, sa.2, ss.831-843, 2025 (SCI-Expanded, Scopus)

14. Neonatal diabetes mellitus is a significant feature of COXPD-24 caused by recessive NARS2 variants

Donis R., Wakeling M. N., Jeffery N., Govier M., Johnson M. B., Hassan S. S., et al.

Diabetic Medicine , cilt.42, sa.11, 2025 (SCI-Expanded, Scopus)

15. The Crucial Role of Body Mass Index on Growth Hormone Stimulation Tests in Children: An Exploration of Potential Gender-Related Differences

ARI H., Celik N. B., SAVAŞ ERDEVE Ş., ÇETİNKAYA S., MURATOĞLU ŞAHİN N.

Clinical Pediatrics , cilt.64, sa.10, ss.1380-1387, 2025 (SCI-Expanded, Scopus)

16. Comparison of the clinical characteristics of children with Silver-Russell syndrome genetically confirmed or not and their response to growth hormone therapy: a national multicenter study

Özgen I. T., Kandemir T., Ylldlz M., POYRAZOĞLU Ş., Şlklar Z., Abseyi N. S., et al.

Journal of Pediatric Endocrinology and Metabolism , cilt.38, sa.8, ss.830-837, 2025 (SCI-Expanded, Scopus)

17. 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

ÇAYIR A., DEMİRBİLEK H., Türkyılmaz A., DEMİRCİOĞLU S., BEREKET A., Darendeliler F., et al.

Hormone Research in Paediatrics , ss.1-9, 2025 (SCI-Expanded, Scopus)

18. Characterization of 35 Novel NR5A1/SF-1 Variants Identified in Individuals With Atypical Sexual Development: The SF1next Study

Naamneh Elzenaty R., Martinez de Lapiscina I., Kouri C., Sauter K., Sommer G., Castaño L., et al.

Journal of Clinical Endocrinology and Metabolism , cilt.110, sa.3, 2025 (SCI-Expanded, Scopus)

19. Evaluation of Growth Characteristics and Final Height of Cases Diagnosed with Noonan Syndrome on Growth Hormone Treatment

ŞIKLAR Z., Berberoğlu M., KIZILCAN ÇETİN S., Yıldız M., DEMİRCİOĞLU S., Darcan Ş., et al.

JCRPE Journal of Clinical Research in Pediatric Endocrinology , cilt.17, sa.1, ss.76-86, 2025 (SCI-Expanded, Scopus, TRDizin)

20. Adrenal hypoandrogenism in adolescents with premature ovarian insufficiency

Bilici M. E., ŞIKLAR Z., ÇETİNKAYA S., ÖZSU E., AYCAN Z., Berberoǧlu M.

Journal of Pediatric Endocrinology and Metabolism , cilt.38, sa.3, ss.262-270, 2025 (SCI-Expanded, Scopus)

21. Rationale for Long-acting Growth Hormone Therapy and Future Aspects

ÇETİNKAYA S., EREN E., Erdoğan F., Darendeliler F.

JCRPE Journal of Clinical Research in Pediatric Endocrinology , cilt.17, sa.1, ss.1-8, 2025 (SCI-Expanded, Scopus, TRDizin)

22. Rare Types of Congenital Adrenal Hyperplasias Other Than 21-hydroxylase Deficiency

İsakoca M., SAVAŞ ERDEVE Ş., ÇETİNKAYA S.

JCRPE Journal of Clinical Research in Pediatric Endocrinology , cilt.17, sa.1, ss.23-32, 2025 (SCI-Expanded, Scopus, TRDizin)

23. Atypical presentation of ACCES syndrome resembling dominant Spondyloepiphyseal dysplasia tarda

Sezer A., Özdemir Z., Özkan E., ÇETİNKAYA S.

American Journal of Medical Genetics, Part A , cilt.194, sa.12, 2024 (SCI-Expanded, Scopus)

24. Decreased calcium permeability caused by biallelic TRPV5 mutation leads to autosomal recessive renal calcium-wasting hypercalciuria

Guleray Lafci N., van Goor M., ÇETİNKAYA S., van der Wijst J., Acun M., Kurt Colak F., et al.

European Journal of Human Genetics , cilt.32, sa.11, ss.1506-1514, 2024 (SCI-Expanded, Scopus)

25. Assessment of the Retinal Nerve Fibre Layer, Retina, and Choroid in Osteogenesis Imperfecta Bewertung der retinalen Nervenfaserschicht, Netzhaut und Aderhaut bei Osteogenesis imperfecta

Keles A., ÇITIRIK M., Karaman S. K., MURATOĞLU ŞAHİN N., ÇETİNKAYA S.

Klinische Monatsblatter fur Augenheilkunde , cilt.241, sa.11, ss.1243-1248, 2024 (SCI-Expanded, Scopus)

26. Preliminary results of thyroid surgery from a tertiary comprehensive children's hospital

Duman Küçükkuray M., KARAMAN A., ÇETİNKAYA S., SAVAŞ ERDEVE Ş., Üner Ç., Genel N., et al.

Journal of Pediatric Surgery Open , cilt.8, 2024 (ESCI, Scopus)

27. High frequency of transient congenital hypothyroidism among infants referred for suspected congenital hypothyroidism from the Turkish National screening program: thyroxine dose may guide the prediction of transients

ÖZER Y., Anık A., SAYILI U., Tercan U., Deveci Sevim R., Güneş S., et al.

Journal of Endocrinological Investigation , cilt.47, sa.9, ss.2213-2224, 2024 (SCI-Expanded, Scopus)

28. 17α Hydroxylase/17,20 lyase deficiency: clinical features and genetic insights from a large Turkey cohort

ŞIKLAR Z., ÇAMTOSUN E., Bolu S., Yildiz M., Akinci A., BAŞ F., et al.

Endocrine , cilt.85, sa.3, ss.1407-1416, 2024 (SCI-Expanded, Scopus)

29. Difficulties Experienced by Mothers in Newly Diagnosed Type 1 Diabetes Mellitus: A Phenomenological Study Yeni Başlangıçlı Tip 1 Diabetes Mellitusta Annelerin Yaşadıkları Güçlükler: Fenomenolojik Bir Çalışma

Taşdelen Baş M., BORA GÜNEŞ N., Yildirim N., ÇETİNKAYA S.

Journal of Nursology , cilt.27, sa.2, ss.120-128, 2024 (ESCI, Scopus, TRDizin)

30. Sterile abscess formation with two different GnRH analogues: Three case reports

Karacan Küçükali G., Özalkak Ş., Peltek Kendirci H. N., Bostancı İ., SAVAŞ ERDEVE Ş., ÇETİNKAYA S.

Trends in Pediatrics , cilt.5, sa.1, ss.20-24, 2024 (Scopus)

31. Clinical features, diagnosis and treatment outcomes of Cushing's disease in children: A multicenter study

TARÇIN G., Çatlı G., ÇETİNKAYA S., EREN E., Kardelen A. D., Akıncı A., et al.

Clinical Endocrinology , cilt.100, sa.1, ss.19-28, 2024 (SCI-Expanded, Scopus)

32. Effect of Adrenocorticotropic Hormone Stimulation on Ischemia-modified Albumin Levels in vivo

MURATOĞLU ŞAHİN N., Esen S., SAVAŞ ERDEVE Ş., NEŞELİOĞLU S., EREL Ö., ÇETİNKAYA S.

JCRPE Journal of Clinical Research in Pediatric Endocrinology , cilt.16, sa.1, ss.84-90, 2024 (SCI-Expanded, Scopus, TRDizin)

33. Stress Induced Hyperglycemia in Early Childhood as a Clue for the Diagnosis of NEUROD1-MODY

Çelik N. B., Güleray Lafcı N., SAVAŞ ERDEVE Ş., ÇETİNKAYA S.

JCRPE Journal of Clinical Research in Pediatric Endocrinology , cilt.16, sa.2, ss.218-223, 2024 (SCI-Expanded, Scopus, TRDizin)

34. Case report: An adolescent female with anosmic hypogonadotropic hypogonadism, intellectual disability, and papillary thyroid carcinoma: heterozygous deletion of TCF12

Celik N. B., Sezer A., Genel N., SAVAŞ ERDEVE Ş., KARAMAN İ., ÇETİNKAYA S.

Frontiers in Endocrinology , cilt.15, 2024 (SCI-Expanded, Scopus)

35. Clinical and genetic characteristics of a large international cohort of individuals with rare NR5A1/SF-1 variants of sex development

Kouri C., Sommer G., Martinez de Lapiscina I., Elzenaty R. N., Tack L. J., Cools M., et al.

eBioMedicine , cilt.99, 2024 (SCI-Expanded, Scopus)

36. Clinical and Laboratory Characteristics of MODY Cases, Genetic Mutation Spectrum and Phenotype-genotype Relationship

ÖZSU E., ÇETİNKAYA S., Bolu S., HATİPOĞLU N., SAVAŞ ERDEVE Ş., EVLİYAOĞLU S. O., et al.

JCRPE Journal of Clinical Research in Pediatric Endocrinology , cilt.16, sa.3, ss.297-305, 2024 (SCI-Expanded, Scopus, TRDizin)

37. Adherence to Growth Hormone Treatment in Children During the COVID-19 Pandemic

EREN E., ÇETİNKAYA S., DENKBOY ÖNGEN Y., Tercan U., Darcan Ş., TURAN H., et al.

JCRPE Journal of Clinical Research in Pediatric Endocrinology , cilt.16, sa.3, ss.256-263, 2024 (SCI-Expanded, Scopus, TRDizin)

38. Long-term follow-up data of patients with Multiple Pituitary Hormone Deficiency Seguimiento a largo plazo de pacientes con Deficiencia Hormonal Hipofisiaria Múltiple

Elvan-Tuz A., BAYRAMOĞLU E., ÇETİNKAYA S.

Andes Pediatrica , cilt.94, sa.6, ss.689-697, 2023 (Scopus)

39. Vitamin D Level of Children with Diabetic Ketoacidosis in Pediatric Intensive Care Unit Pediatrik Yoğun Bakım Ünitesindeki Diyabetik Ketoasidozlu Çocukların D Vitamini Düzeylerinin Değerlendirilmesi

UYSAL YAZICI M., Ozel E., Torun E. G., SAVAŞ ERDEVE Ş., ÇETİNKAYA S.

Genel Tip Dergisi , cilt.33, sa.5, ss.523-526, 2023 (Scopus, TRDizin)

40. Reclassification of two germline DICER1 splicing variants leads to DICER1 syndrome diagnosis

Apellaniz-Ruiz M., Sabbaghian N., Chong A., de Kock L., ÇETİNKAYA S., BAYRAMOĞLU E., et al.

Familial Cancer , cilt.22, sa.4, ss.487-493, 2023 (SCI-Expanded, Scopus)

41. 3M syndrome: Evaluating the clinical and laboratory features and the response of the growth hormone treatment: Single center experience

Karacan Küçükali G., KESKİN M., AYCAN Z., SAVAŞ ERDEVE Ş., ÇETİNKAYA S.

European Journal of Medical Genetics , cilt.66, sa.10, 2023 (SCI-Expanded, Scopus)

42. Optical coherence tomography angiography findings in pediatric patients with graves ophthalmopathy

Ceylanoglu K. S., Sen E. M., Karamert S. S., SAVAŞ ERDEVE Ş., ÇETİNKAYA S.

International Ophthalmology , cilt.43, sa.10, ss.3609-3614, 2023 (SCI-Expanded, Scopus)

43. The Level of Inflammatory Markers and Their Relationship with Fat Tissue Distribution in Children with Obesity and Type 2 Diabetes Mellitus

Ertürk B. A., GÜLBAHAR Ö., Şahap S. K., Bulut T. S. D., ÇETİNKAYA S., SAVAŞ ERDEVE Ş.

Turkish Archives of Pediatrics , cilt.58, sa.5, ss.485-493, 2023 (ESCI, Scopus, TRDizin)

44. A National Multicenter Study of Leptin and Leptin Receptor Deficiency and Systematic Review

Besci Ö., Fırat S. N., Özen S., ÇETİNKAYA S., Akın L., Kör Y., et al.

Journal of Clinical Endocrinology and Metabolism , cilt.108, sa.9, ss.2371-2388, 2023 (SCI-Expanded, Scopus)

45. Evaluation of aggression level in adolescent girls with classical congenital adrenal hyperplasia

Isik R. O., KIZILCAN ÇETİN S., ÇETİNKAYA S., Berberoglu M., ŞIKLAR Z., ÖZSU E., et al.

Clinical Endocrinology , cilt.99, sa.2, ss.135-141, 2023 (SCI-Expanded, Scopus)

46. The Effects of Thyroid Hormone Levels on Patent Ductus Arteriosus Closure in Newborns Yenidoğanlarda Tiroid Hormon Düzeylerinin Patent Ductus Arteriosus Kapanması Üzerine Etkisi

Kaya B., Akduman H., DİLLİ D., ÇETİNKAYA S., ÖKTEM A., ÖRÜN U. A., et al.

Medeniyet Medical Journal , cilt.38, sa.3, ss.187-192, 2023 (Scopus, TRDizin)

47. Hemolytic Anemia due to Glucose 6 Phosphate Dehydrogenase Deficiency Triggered by Type 1 Diabetes Mellitus

Orman B., ÇETİNKAYA S., Öner N., Akçaboy M., FETTAH A., Lafcı N. G., et al.

JCRPE Journal of Clinical Research in Pediatric Endocrinology , cilt.15, sa.4, ss.417-420, 2023 (SCI-Expanded, Scopus, TRDizin)

48. Editorial: Recent advances in diagnosis and treatment of congenital adrenal hyperplasia due to 21-hydroxylase deficiency

ÇETİNKAYA S.

Frontiers in Endocrinology , cilt.14, 2023 (SCI-Expanded, Scopus)

49. Unfavorable Effects of Low-carbonhydrate Diet in a Pediatric Patient with Type 1 Diabetes Mellitus

Güleryüz C., Eker E., Küçükali G. K., Şakar M., GENÇ F., MURATOĞLU ŞAHİN N., et al.

JCRPE Journal of Clinical Research in Pediatric Endocrinology , cilt.15, sa.4, ss.444-448, 2023 (SCI-Expanded, Scopus, TRDizin)

50. Genotype of congenital adrenal hyperplasia patients with testicular adrenal rest tumor

AYCAN Z., KESKİN M., Lafcı N. G., SAVAŞ ERDEVE Ş., BAŞ F., POYRAZOĞLU Ş., et al.

European Journal of Medical Genetics , cilt.65, sa.12, 2022 (SCI-Expanded, Scopus)

51. Evaluation of permanent and transient congenital hypothyroidism in cases referred from National Neonatal Screening Program

Donbaloğlu Z., ÇETİNKAYA S., Aycan Z., Karacan Küçükali G., Şakar M., SAVAŞ ERDEVE Ş.

Journal of Paediatrics and Child Health , cilt.58, sa.8, ss.1431-1438, 2022 (SCI-Expanded, Scopus)

52. Status of Central Precocious Puberty Cases at the Onset of Coronavirus Disease 2019 Pandemic: A Single-Center Experience

Orman B., Esen S., KESKİN M., MURATOĞLU ŞAHİN N., SAVAŞ ERDEVE Ş., ÇETİNKAYA S.

Turkish Archives of Pediatrics , cilt.57, sa.3, ss.349-353, 2022 (Scopus, TRDizin)

53. Insights From Long-term Follow-up of a Girl With Adrenal Insufficiency and Sphingosine-1-Phosphate Lyase Deficiency

Maharaj A., GÜRAN T., Buonocore F., Achermann J. C., Metherell L., Prasad R., et al.

Journal of the Endocrine Society , cilt.6, sa.5, 2022 (ESCI, Scopus)

54. PLXNB1 mutations in the etiology of idiopathic hypogonadotropic hypogonadism

Welch B. A., Cho H., UÇAKTÜRK S. A., Farmer S. M., ÇETİNKAYA S., ABACI A., et al.

Journal of Neuroendocrinology , cilt.34, sa.4, 2022 (SCI-Expanded, Scopus)

55. Gender incongruence in children and adolescents. Çocuk ve adolesanlarda cinsiyet uyuşmazlığı

Aycan Z., Başar K., BÖBER E., ÇETİNKAYA S., Darcan Ş., Darendeliler F., et al.

Cocuk Sagligi ve Hastaliklari Dergisi , cilt.65, sa.2, ss.47-53, 2022 (Scopus)

56. A major health problem facing immigrant children: Nutritional rickets

KURNAZ E., ÇETİNKAYA S., Elmaoǧullarl S., Arasll Yllmaz A., MURATOĞLU ŞAHİN N., KESKİN M., et al.

Journal of Pediatric Endocrinology and Metabolism , cilt.35, sa.2, ss.223-229, 2022 (SCI-Expanded, Scopus)

57. Evaluation of growth and effect of metabolic control on growth velocity in children with type 1 diabetes mellitus Tip 1 diyabetes mellituslu çocuklarda büyümenin değerlendirilmesi ve metabolik kontrolün büyüme hızına etkisi

Kaya N. G., Önder A., ÇETİNKAYA S., Aycan Z.

Pamukkale Medical Journal , cilt.15, sa.4, ss.772-778, 2022 (Scopus, TRDizin)

58. Sleep disorder and behavior problems in children with type 1 diabetes mellitus

Ilter Bahadur E., Özalkak S., Özdemir A. A., ÇETİNKAYA S., ÖZMERT E. N.

Journal of Pediatric Endocrinology and Metabolism , cilt.35, sa.1, ss.29-38, 2022 (SCI-Expanded, Scopus)

59. The role of self-discontentment and impulsivity for youth smoking behavior, nicotine dependence and future smoking intention in a clinical sample of Turkish adolescents

UYGUN S. D., AYGÜN ARI D., KONŞUK ÜNLÜ H., ÇETİNKAYA S.

Turkish Journal of Pediatrics , cilt.64, sa.4, ss.694-707, 2022 (SCI-Expanded, Scopus, TRDizin)

60. Diagnostic Value of Bilateral Petrosal Sinus Sampling in Children with Cushing Disease: A Multi-center Study

TURAN H., Çatlı G., Kardelen A. D., BÖBER E., Akıncı A., ÇETİNKAYA S., et al.

JCRPE Journal of Clinical Research in Pediatric Endocrinology , cilt.14, sa.1, ss.29-36, 2022 (SCI-Expanded, Scopus, TRDizin)

61. A retrospective analysis of endocrine disease in sphingosine-1-phosphate lyase insufficiency: case series and literature review

Maharaj A., Kwong R., Williams J., Smith C., Storr H., Krone R., et al.

Endocrine Connections , cilt.11, sa.8, 2022 (SCI-Expanded, Scopus)

62. Urinary levels of phthalate esters and heavy metals in adolescents with thyroid colloid cysts

YALÇIN Ş., Erdal İ., ÇETİNKAYA S., OĞUZ B.

International Journal of Environmental Health Research , cilt.32, sa.6, ss.1359-1372, 2022 (SCI-Expanded, Scopus)

63. The effect of GnRH stimulation on AMH regulation in central precocious puberty and isolated premature thelarche

MURATOĞLU ŞAHİN N., ÖZCAN H. N., Yilmaz A. A., SAVAŞ ERDEVE Ş., ÇETİNKAYA S., Aycan Z.

Journal of Pediatric Endocrinology and Metabolism , cilt.34, sa.11, ss.1385-1391, 2021 (SCI-Expanded, Scopus)

64. Effects of subclinical emotional and behavioral problems on metabolic control in adolescents with type 1 diabetes: Role of maternal and adolescent personality traits

UYGUN S. D., Şakar M., SAVAŞ ERDEVE Ş., ÇETİNKAYA S.

Archives de Pediatrie , cilt.28, sa.8, ss.626-631, 2021 (SCI-Expanded, Scopus)

65. Mild phenotype in two siblings with a missense GHR variant

Sarlkaya Özdemir B., ÇETİNKAYA S., Güleray Lafcl N., Sakar M., Karacan Küçükali G., Elmaoǧullari S., et al.

Journal of Pediatric Endocrinology and Metabolism , cilt.34, sa.10, ss.1349-1354, 2021 (SCI-Expanded, Scopus)

66. Hypergonadotrophic hypogonadism in a patient with transaldolase deficiency: novel mutation in the pentose phosphate pathway

Lafcı N. G., Colak F. K., Sahin G., Sakar M., ÇETİNKAYA S., SAVAŞ ERDEVE Ş.

Hormones , cilt.20, sa.3, ss.581-585, 2021 (SCI-Expanded, Scopus)

67. Retrospective evaluation of patients with X-linked adrenoleukodystrophy with a wide range of clinical presentations: A single center experience

Olgac A., Kasapkara Ç. S., Derinkuyu B., YÜKSEL D., ÇETİNKAYA S., Aksoy A., et al.

Journal of Pediatric Endocrinology and Metabolism , cilt.34, sa.9, ss.1169-1179, 2021 (SCI-Expanded, Scopus)

68. Evaluation of the pathophysiological role of Fetuin A levels in adolescents with polycystic ovary syndrome

BAYRAMOĞLU E., ÇETİNKAYA S., Özalkak S., KURNAZ E., Demirci G., ÖZTÜRK H. S., et al.

Journal of Pediatric Endocrinology and Metabolism , cilt.34, sa.7, ss.911-916, 2021 (SCI-Expanded, Scopus)

69. Long-term clinical follow-up of patients with familial hypomagnesemia with secondary hypocalcemia

BAYRAMOĞLU E., KESKİN M., Aycan Z., SAVAŞ ERDEVE Ş., ÇETİNKAYA S.

JCRPE Journal of Clinical Research in Pediatric Endocrinology , cilt.13, sa.3, ss.300-307, 2021 (SCI-Expanded, Scopus, TRDizin)

70. Perinatal outcomes of high-dose vitamin d administration in the last trimester Son trimesterde yüksek doz d vitamini uygulamasının perinatal sonuçları

Küçükali G. K., KESKİN M., SAVAŞ ERDEVE Ş., ÇETİNKAYA S.

Turkish Journal of Obstetrics and Gynecology , cilt.18, sa.2, ss.159-162, 2021 (ESCI, Scopus, TRDizin)

71. A case of prohormone convertase deficiency diagnosed with type 2 diabetes

Küçükali G. K., SAVAŞ ERDEVE Ş., ÇETİNKAYA S., KESKİN M., BULUŞ A. D., Aycan Z.

Turkish Archives of Pediatrics , cilt.56, sa.1, ss.81-84, 2021 (ESCI, Scopus, TRDizin)

72. Langerhans Cell Histiocytosis with Isolated Central Diabetes Insipidus, Low Grade Fever and Sellar Erosion

Okur İ., ARI H., ÇETİNKAYA S., Derinkuyu B. E., Çağlar G., Çınar H. G., et al.

Trends in Pediatrics , cilt.2, sa.2, ss.104-108, 2021 (Scopus)

73. Evaluation of children and adolescents with thyroid nodules: A single center experience

Elmaoğulları S., Özalkak Ş., ÇETİNKAYA S., KARAMAN İ., Üner Ç., Arda N., et al.

JCRPE Journal of Clinical Research in Pediatric Endocrinology , cilt.13, sa.3, ss.276-284, 2021 (SCI-Expanded, Scopus, TRDizin)

74. A rare cause of salt-wasting in early infancy: Transient pseudohypoaldosteronism

Ceylan D., BAYRAMOĞLU E., POLAT E., SAVAŞ ERDEVE Ş., ÇETİNKAYA S., Aycan Z.

Turkish Archives of Pediatrics , cilt.56, sa.1, ss.75-77, 2021 (ESCI, Scopus, TRDizin)

75. Clinical characteristics of 46, xx males with congenital adrenal hyperplasia

SAVAŞ ERDEVE Ş., AYCAN Z., ÇETİNKAYA S., Öztürk A. P., BAŞ F., POYRAZOĞLU Ş., et al.

JCRPE Journal of Clinical Research in Pediatric Endocrinology , cilt.13, sa.2, ss.180-186, 2021 (SCI-Expanded, Scopus, TRDizin)

76. A Newborn Admitted with Hyponatremia and Hyperkalemia Clinic and Diagnosed with Primary Hypoaldosteronism

Şakar M., ÇETİNKAYA S., Arifoğlu Barış İ., ÖKTEM A., ZENCİROĞLU A., Bundak R., et al.

Trends in Pediatrics , cilt.2, sa.2, ss.94-98, 2021 (Scopus)

77. Evaluation of growth hormone results in different diagnosis and trend over 10 year of follow-up: A single center experience

Aycan Z., Yılmaz A. A., Yel S., SAVAŞ ERDEVE Ş., ÇETİNKAYA S.

JCRPE Journal of Clinical Research in Pediatric Endocrinology , cilt.13, sa.3, ss.332-341, 2021 (SCI-Expanded, Scopus, TRDizin)

78. Clinical Management in Systemic Type Pseudohypoaldosteronism Due to SCNN1B Variant and Literature Review

Küçükali G. K., ÇETİNKAYA S., Tunç G., Melek Oğuz M., ÇELİK N., Akkaş K. Y., et al.

JCRPE Journal of Clinical Research in Pediatric Endocrinology , cilt.13, sa.4, ss.446-451, 2021 (SCI-Expanded, Scopus, TRDizin)

79. Evaluation of gonadotropin responses and response times according to two different cut-off values in luteinizing hormone releasing hormone stimulation test in girls

Özalkak Ş., ÇETİNKAYA S., Budak F. C., SAVAŞ ERDEVE Ş., Aycan Z.

Indian Journal of Endocrinology and Metabolism , cilt.24, sa.5, ss.410-415, 2020 (Scopus)

80. Nationwide Turkish cohort study of hypophosphatemic rickets

ŞIKLAR Z., DEMİRCİOĞLU S., BEREKET A., BAŞ F., GÜRAN T., Akberzade A., et al.

JCRPE Journal of Clinical Research in Pediatric Endocrinology , cilt.12, sa.2, ss.150-159, 2020 (SCI-Expanded, Scopus, TRDizin)

81. Serum Fetuin-A and Insulin Levels in Classic Congenital Adrenal Hyperplasia

KURNAZ E., ÇETİNKAYA S., Özalkak Ş., BAYRAMOĞLU E., Demirci G., ÖZTÜRK H. S., et al.

Hormone and Metabolic Research , cilt.52, sa.9, ss.654-659, 2020 (SCI-Expanded, Scopus)

82. Effects of 5-hydroxymethylfurfural on pubertal development of female wistar rats

Elmaoğulları S., Kadan E., ANADOL E., Gökçeoğlu A., ÇETİNKAYA S., Yarım G. F., et al.

JCRPE Journal of Clinical Research in Pediatric Endocrinology , cilt.12, sa.1, ss.79-85, 2020 (SCI-Expanded, Scopus, TRDizin)

83. Effect of gonadotropin-releasing hormone analog treatment on final height in girls aged 6–10 years with central precocious and early puberty Gonadotropin releasing hormon analog tedavisinin santral erken ergenlikli 6–10 yaş arası kızlarda final boya etkisi

Onat P. Ş., SAVAŞ ERDEVE Ş., ÇETİNKAYA S., Aycan Z.

Turkish Archives of Pediatrics , cilt.55, sa.4, ss.361-369, 2020 (ESCI, Scopus, TRDizin)

84. The alteration of IGF-1 levels and relationship between IGF-1 levels and growth velocity during GnRH analogue therapy

MURATOĞLU ŞAHİN N., Peltek Kendirci H. N., ÇETİNKAYA S., SAVAŞ ERDEVE Ş., Aycan Z.

Journal of Pediatric Endocrinology and Metabolism , cilt.33, sa.1, ss.113-120, 2020 (SCI-Expanded, Scopus)

85. Clitoromegaly caused by ovarian stimulation in a preterm newborn: Ovarian hyperstimulation syndrome of preterm babies

BAYRAMOĞLU E., SAVAŞ ERDEVE Ş., Derinkuyu B. E., ÇELİK İ. H., ÇETİNKAYA S., Aycan Z.

Turkish Journal of Pediatrics , cilt.62, sa.6, ss.1088-1093, 2020 (SCI-Expanded, Scopus, TRDizin)

86. Evaluation of thiol/disulfide homeostasis in pediatric patients with diabetic ketoacidosis

YAZICI M., Ayar G., ÇETİNKAYA S., KESKİN M., Azapağası E., NEŞELİOĞLU S., et al.

Combinatorial Chemistry and High Throughput Screening , cilt.23, sa.3, ss.185-190, 2020 (SCI-Expanded, Scopus)

87. Functional assessment of variants associated with Wolfram syndrome

Riachi M., Yilmaz S., KURNAZ E., Aycan Z., ÇETİNKAYA S., Tranebjærg L., et al.

Human Molecular Genetics , cilt.28, sa.22, ss.3815-3824, 2019 (SCI-Expanded, Scopus)

88. Antimüllerian hormone levels of infants with premature thelarche

MURATOĞLU ŞAHİN N., BAYRAMOĞLU E., Özcan H. N., KURNAZ E., KESKİN M., SAVAŞ ERDEVE Ş., et al.

JCRPE Journal of Clinical Research in Pediatric Endocrinology , cilt.11, sa.3, ss.287-292, 2019 (SCI-Expanded, Scopus, TRDizin)

89. Cases referred from the turkish national screening program: Frequency of congenital hypothyroidism and etiological distribution

Donbaloğlu Z., SAVAŞ ERDEVE Ş., ÇETİNKAYA S., Aycan Z.

JCRPE Journal of Clinical Research in Pediatric Endocrinology , cilt.11, sa.3, ss.240-246, 2019 (SCI-Expanded, Scopus, TRDizin)

90. Rare Cause of Infantile Hypercalcemia: A Novel Mutation in the SLC34A1 Gene

KURNAZ E., SAVAŞ ERDEVE Ş., ÇETİNKAYA S., Aycan Z.

Hormone Research in Paediatrics , cilt.91, sa.4, ss.278-284, 2019 (SCI-Expanded, Scopus)

91. Comparison of treatment regimens in management of severe hypercalcemia due to vitamin D intoxication in children

DEMİR K., DÖNERAY H., Kara C., Atay Z., ÇETİNKAYA S., Çayır A., et al.

JCRPE Journal of Clinical Research in Pediatric Endocrinology , cilt.11, sa.2, ss.140-148, 2019 (SCI-Expanded, Scopus, TRDizin)

92. Experience of intravenous calcium treatment and long-term responses to treatment in a patient with hereditary Vitamin D-resistant rickets resulting from a novel mutation

BAYRAMOĞLU E., SAVAŞ ERDEVE Ş., Shi Y., KESKİN M., ÇETİNKAYA S., KURNAZ E., et al.

Journal of Pediatric Endocrinology and Metabolism , cilt.32, sa.6, ss.647-651, 2019 (SCI-Expanded, Scopus)

93. Detection of the SRY gene in patients with Turner Syndrome

KURNAZ E., ÇETİNKAYA S., SAVAŞ ERDEVE Ş., Aycan Z.

Journal of Gynecology Obstetrics and Human Reproduction , cilt.48, sa.4, ss.265-267, 2019 (Scopus)

94. Bone loss in pediatric survivors of acute lymphoblastic leukemia

Donmez A. D., Isik P., ÇETİNKAYA S., Yarali N.

Eurasian Journal of Medicine , cilt.51, sa.1, ss.38-41, 2019 (Scopus, TRDizin)

95. Role of ischemia modified albumin serum levels as an oxidative stress marker in children with diabetic ketoacidosis

YAZICI M., Ayar G., SAVAŞ ERDEVE Ş., Azapağası E., NEŞELİOĞLU S., EREL Ö., et al.

Combinatorial Chemistry and High Throughput Screening , cilt.22, sa.8, ss.577-581, 2019 (SCI-Expanded, Scopus)

96. Congenital long-QT syndrome in type 1 diabetes: A unique association

KURNAZ E., SAVAŞ ERDEVE Ş., ÖZGÜR S., KESKİN M., Özbudak P., ÇETİNKAYA S., et al.

Turkish Journal of Pediatrics , cilt.61, sa.5, ss.791-793, 2019 (SCI-Expanded, Scopus, TRDizin)

97. The effect of 2000 ıu/day vitamin D supplementation on insulin resistance and cardiovascular risk parameters in vitamin D deficient obese adolescents

Bilici M. E., SAVAŞ ERDEVE Ş., ÇETİNKAYA S., Aycan Z.

The Turkish journal of pediatrics , cilt.61, sa.5, ss.723-732, 2019 (SCI-Expanded, Scopus, TRDizin)

98. Near final height in patients with idiopathic growth hormone deficiency: A single-centre experience

KURNAZ E., ÇETİNKAYA S., Aycan Z.

Journal of Paediatrics and Child Health , cilt.54, sa.11, ss.1221-1226, 2018 (SCI-Expanded, Scopus)

99. SHOX gene deletion screening by FISH in children with short stature and Madelung deformity and their characteristics

KURNAZ E., SAVAŞ ERDEVE Ş., ÇETİNKAYA S., Aycan Z.

Journal of Pediatric Endocrinology and Metabolism , cilt.31, sa.11, ss.1273-1278, 2018 (SCI-Expanded, Scopus)

100. Follow-up in children with non-obese and non-autoimmune subclinical hypothyroidism

Ergin Z., SAVAŞ ERDEVE Ş., KURNAZ E., ÇETİNKAYA S., Aycan Z.

Journal of Pediatric Endocrinology and Metabolism , cilt.31, sa.10, ss.1133-1138, 2018 (SCI-Expanded, Scopus)

101. Subnormal growth velocity and related factors during GnRH analog therapy for idiopathic central precocious puberty

MURATOĞLU ŞAHİN N., Dikmen A. U., ÇETİNKAYA S., Aycan Z.

JCRPE Journal of Clinical Research in Pediatric Endocrinology , cilt.10, sa.3, ss.239-246, 2018 (SCI-Expanded, Scopus, TRDizin)

102. Investigation of MKRN3 mutation in patients with familial central precocious puberty

Aycan Z., SAVAŞ ERDEVE Ş., ÇETİNKAYA S., KURNAZ E., KESKİN M., MURATOĞLU ŞAHİN N., et al.

JCRPE Journal of Clinical Research in Pediatric Endocrinology , cilt.10, sa.3, ss.223-229, 2018 (SCI-Expanded, Scopus, TRDizin)

103. Renal complications of lipodystrophy: A closer look at the natural history of kidney disease

Akinci B., Unlu S. M., Celik A., Simsir I. Y., Sen S., NUR B., et al.

Clinical Endocrinology , cilt.89, sa.1, ss.65-75, 2018 (SCI-Expanded, Scopus)

104. Clinical follow-up data and the rate of development of precocious and rapidly progressive puberty in patients with premature thelarche

Çiçek D., SAVAŞ ERDEVE Ş., ÇETİNKAYA S., Aycan Z.

Journal of Pediatric Endocrinology and Metabolism , cilt.31, sa.3, ss.305-312, 2018 (SCI-Expanded, Scopus)

105. A patient with proopiomelanocortin deficiency: An increasingly important diagnosis to make

ÇETİNKAYA S., GÜRAN T., KURNAZ E., KESKİN M., Sağsak E., SAVAŞ ERDEVE Ş., et al.

JCRPE Journal of Clinical Research in Pediatric Endocrinology , cilt.10, sa.1, ss.68-73, 2018 (SCI-Expanded, Scopus, TRDizin)

106. Sever’s disease in a patient receiving growth hormone with no causative relation

KURNAZ E., SAVAŞ ERDEVE Ş., Aycan Z., ÇETİNKAYA S.

Journal of Clinical and Diagnostic Research , cilt.12, sa.3, 2018 (Scopus)

107. Clinical and genetic characterisation of a series of patients with triple A syndrome

KURNAZ E., Duminuco P., Aycan Z., SAVAŞ ERDEVE Ş., MURATOĞLU ŞAHİN N., KESKİN M., et al.

European Journal of Pediatrics , cilt.177, sa.3, ss.363-369, 2018 (SCI-Expanded, Scopus)

108. Vaginal bleeding and a giant ovarian cyst in an infant with 21-hydroxylase deficiency

MURATOĞLU ŞAHİN N., BAYRAMOĞLU E., ÇETİNKAYA S., SAVAŞ ERDEVE Ş., KARAMAN A., Akdoǧan M. P., et al.

Journal of Pediatric Endocrinology and Metabolism , cilt.31, sa.2, ss.229-233, 2018 (SCI-Expanded, Scopus)

109. Response to growth hormone treatment in very young patients with growth hormone deficiencies and mini-puberty

ÇETİNKAYA S., POYRAZOĞLU Ş., BAŞ F., Ercan O., Ylldlz M., Adal E., et al.

Journal of Pediatric Endocrinology and Metabolism , cilt.31, sa.2, ss.175-184, 2018 (SCI-Expanded, Scopus)

110. Low hemoglobin a1c levels in a patient with diabetic ketoacidosis: Fulminant type 1 diabetes mellitus

KESKİN M., SAVAŞ ERDEVE Ş., ÇETİNKAYA S., Aycan Z.

Turkish Journal of Pediatrics , cilt.60, sa.2, ss.201-205, 2018 (SCI-Expanded, Scopus, TRDizin)

111. A newborn with transient diabetes mellitus accompanied by ketoacidosis attributable to a ZFP57 mutation

Iyigun F., ÖZCAN B., KULALI F., ÇELİK İ. H., ÇETİNKAYA S., Bas A. Y., et al.

Journal of Tropical Pediatrics , cilt.63, sa.5, ss.399-401, 2017 (SCI-Expanded, Scopus)

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

SAVAŞ ERDEVE Ş., ÇETİNKAYA S., Abali Z. Y., POYRAZOĞLU Ş., BAŞ F., Berberoǧlu M., et al.

Journal of Pediatric Endocrinology and Metabolism , cilt.30, sa.7, ss.759-766, 2017 (SCI-Expanded, Scopus)

113. A rare cause of short stature: 3M syndrome in a patient with novel mutation in OBSL1 gene

KESKİN M., MURATOĞLU ŞAHİN N., KURNAZ E., BAYRAMOĞLU E., SAVAŞ ERDEVE Ş., Aycan Z., et al.

JCRPE Journal of Clinical Research in Pediatric Endocrinology , cilt.9, sa.1, ss.91-94, 2017 (SCI-Expanded, Scopus, TRDizin)

114. AMH levels in girls with various pubertal problems

SAVAŞ ERDEVE Ş., Sagsak E., KESKİN M., ÇETİNKAYA S., Aycan Z.

Journal of Pediatric Endocrinology and Metabolism , cilt.30, sa.3, ss.333-335, 2017 (SCI-Expanded, Scopus)

115. Complete androgen insensitivity syndrome associated with bilateral sertoli cell adenomas and unilateral paratesticular leiomyoma: A case report

SAVAŞ ERDEVE Ş., Aycan Z., KESKİN M., ÇETİNKAYA S., KARAMAN A., Apaydın S., et al.

Turkish Journal of Pediatrics , cilt.58, sa.6, ss.650-653, 2017 (SCI-Expanded, Scopus, TRDizin)

116. Conventional insulin pump therapy in two neonatal diabetes patients harboring the homozygous PTF1A enhancer mutation: Need for a novel approach for the management of neonatal diabetes

KURNAZ E., Aycan Z., Yıldırım N., ÇETİNKAYA S.

Turkish Journal of Pediatrics , cilt.59, sa.4, ss.458-462, 2017 (SCI-Expanded, Scopus, TRDizin)

117. Treatment experience and long-term follow-up data in two severe neonatal hyperparathyroidism cases

SAVAŞ ERDEVE Ş., Sagsak E., KESKİN M., Magdelaine C., Lienhardt-Roussie A., KURNAZ E., et al.

Journal of Pediatric Endocrinology and Metabolism , cilt.29, sa.9, ss.1103-1110, 2016 (SCI-Expanded, Scopus)

118. The growth characteristics of patients with Noonan syndrome: Results of three years of growth hormone treatment: A nationwide multicenter study

ŞIKLAR Z., Genens M., POYRAZOĞLU Ş., BAŞ F., Darendeliler F., Bundak R., et al.

JCRPE Journal of Clinical Research in Pediatric Endocrinology , cilt.8, sa.3, ss.305-312, 2016 (SCI-Expanded, Scopus, TRDizin)

119. Efficacy and safety of pamidronate in children with vitamin D intoxication

Kara C., ÇETİNKAYA S., Gündüz S., Can Yılmaz G., Aycan Z., Aydın M.

Pediatrics International , cilt.58, sa.7, ss.562-568, 2016 (SCI-Expanded, Scopus)

120. Do the Anti-Müllerian Hormone Levels of Adolescents with Polycystic Ovary Syndrome, Those Who Are at Risk for Developing Polycystic Ovary Syndrome, and Those Who Exhibit Isolated Oligomenorrhea Differ from Those of Adolescents with Normal Menstrual Cycles?

SAVAŞ ERDEVE Ş., KESKİN M., Sagsak E., Cenesiz F., ÇETİNKAYA S., Aycan Z.

Hormone Research in Paediatrics , cilt.85, sa.6, ss.406-411, 2016 (SCI-Expanded, Scopus)

121. The etiology and clinical features of non-CAH gonadotropin-independent precocious puberty: A multicenter study

Atay Z., Yesilkaya E., SAVAŞ ERDEVE Ş., DEMİRCİOĞLU S., Akın L., EREN E., et al.

Journal of Clinical Endocrinology and Metabolism , cilt.101, sa.5, ss.1980-1988, 2016 (SCI-Expanded, Scopus)

122. Maturity onset diabetes of youth (MODY) in Turkish children: Sequence analysis of 11 causative genes by next generation sequencing

Aǧladioǧlu S. Y., Aycan Z., ÇETİNKAYA S., Baş V. N., Önder A., Peltek Kendirci H. N., et al.

Journal of Pediatric Endocrinology and Metabolism , cilt.29, sa.4, ss.487-496, 2016 (SCI-Expanded, Scopus)

123. Gonadoblastoma in a patient with 46, XY complete gonadal dysgenesis

KESKİN M., SAVAŞ ERDEVE Ş., KURNAZ E., ÇETİNKAYA S., KARAMAN A., Apaydın S., et al.

Turkish Journal of Pediatrics , cilt.58, sa.5, ss.538-540, 2016 (SCI-Expanded, Scopus, TRDizin)

124. A case with atrophic autoimmune thyroiditis-related hypothyroidism causing multisystem involvement in early childhood

KURNAZ E., SAVAŞ ERDEVE Ş., KESKİN M., Doğan V., ÇETİNKAYA S., Aycan Z.

Turkish Journal of Pediatrics , cilt.58, sa.4, ss.446-451, 2016 (SCI-Expanded, Scopus, TRDizin)

125. The first childhood case with coexisting hashimoto thyroiditis, vitiligo and autoimmune hepatitis

KESKİN M., SAVAŞ ERDEVE Ş., Özbay-Hoşnut F., KURNAZ E., ÇETİNKAYA S., Aycan Z.

Turkish Journal of Pediatrics , cilt.58, sa.4, ss.432-435, 2016 (SCI-Expanded, Scopus, TRDizin)

126. Molecular analysis of PROP1, POU1F1, LHX3, and HESX1 in Turkish patients with combined pituitary hormone deficiency: a multicenter study

BAŞ F., UYGUNER Z. O., Darendeliler F., Aycan Z., Çetinkaya E., Berberoğlu M., et al.

Endocrine , cilt.49, sa.2, ss.479-491, 2015 (SCI-Expanded, Scopus)

127. Risk factors affecting the development of nephrocalcinosis, the most common complication of hypophosphatemic rickets

KESKİN M., Savaş-Erdeve E., Saʇsak E., ÇETİNKAYA S., Aycan Z.

Journal of Pediatric Endocrinology and Metabolism , cilt.28, sa.11-12, ss.1333-1337, 2015 (SCI-Expanded, Scopus)

128. Selenium, zinc, and copper levels and their relation with HbA1c status in children with type 1 diabetes mellitus

Özenç S., Saldir M., Sarı E., ÇETİNKAYA S., Yeşilkaya Ş., Babacan O., et al.

International Journal of Diabetes in Developing Countries , cilt.35, sa.4, ss.514-518, 2015 (SCI-Expanded, Scopus)

129. Effects of GnRH analogue treatment on anterior pituitary hormones in children with central precocious puberty

Peltek Kendirci H. N., Aʇladloʇlu S. Y., Önder A., Baş V. N., ÇETİNKAYA S., Aycan Z.

Journal of Pediatric Endocrinology and Metabolism , cilt.28, sa.9-10, ss.1145-1151, 2015 (SCI-Expanded, Scopus)

130. 17α-Hydroylase/17,20-lyase deficiency related to P.Y27∗(c.81C>A) mutation in CYP17A1 gene

KESKİN M., Uʇurlu A. K., SAVAŞ ERDEVE Ş., Saʇsak E., Akyüz S. G., ÇETİNKAYA S., et al.

Journal of Pediatric Endocrinology and Metabolism , cilt.28, sa.7-8, ss.919-921, 2015 (SCI-Expanded, Scopus)

131. 17βHSD-3 enzyme deficiency due to novel mutations in the HSD17B3 gene diagnosed in a neonate

Sagsak E., Aycan Z., SAVAŞ ERDEVE Ş., KESKİN M., ÇETİNKAYA S., Karaer K.

Journal of Pediatric Endocrinology and Metabolism , cilt.28, sa.7-8, ss.957-959, 2015 (SCI-Expanded, Scopus)

132. The evaluation of transient hypothyroidism in patients diagnosed with congenital hypothyroidism

Peltek Kendirci H. N., Aycan Z., Sağsak E., KESKİN M., ÇETİNKAYA S.

Turkish Journal of Medical Sciences , cilt.45, sa.4, ss.745-750, 2015 (SCI-Expanded, Scopus, TRDizin)

133. The use of pamidronate for acute vitamin D intoxication, clinical experience with three cases

Sagsak E., SAVAŞ ERDEVE Ş., KESKİN M., ÇETİNKAYA S., Aycan Z.

Journal of Pediatric Endocrinology and Metabolism , cilt.28, sa.5-6, ss.709-712, 2015 (SCI-Expanded, Scopus)

134. Evaluating the Efficacy of Treatment with a GnRH Analogue in Patients with Central Precocious Puberty

Kendirci H. N. P., Aʇladioʇlu S. Y., Baş V. N., Önder A., ÇETİNKAYA S., Aycan Z.

International Journal of Endocrinology , cilt.2015, 2015 (SCI-Expanded, Scopus)

135. An uncommon cause of hypoglycemia: Insulin autoimmune syndrome

SAVAŞ ERDEVE Ş., Agladioglu S. Y., Onder A., Kendirci H. N. P., Bas V. N., Sagsak E., et al.

Hormone Research in Paediatrics , cilt.82, sa.4, ss.278-282, 2014 (SCI-Expanded, Scopus)

136. A common thyroid peroxidase gene mutation (G319R) in Turkish patients with congenital hypothyroidism could be due to a founder effect

Baş V. N., Aycan Z., Cangul H., Kendall M., Aǧladioǧlu S. Y., ÇETİNKAYA S., et al.

Journal of Pediatric Endocrinology and Metabolism , cilt.27, sa.3-4, ss.383-387, 2014 (SCI-Expanded, Scopus)

137. What has national screening program changed in cases with congenital hypothyroidism?

Özgelen Ş., Baş V. N., ÇETİNKAYA S., Aycan Z.

Iranian Journal of Pediatrics , cilt.24, sa.3, ss.255-260, 2014 (SCI-Expanded, Scopus)

138. Diseases accompanying congenital hypothyroidism

Baş V. N., Özgelen Ş., ÇETİNKAYA S., Aycan Z.

Journal of Pediatric Endocrinology and Metabolism , cilt.27, sa.5-6, ss.485-489, 2014 (SCI-Expanded, Scopus)

139. Adherence to growth hormone therapy: Results of a multicenter study

Aydin B. K., Aycan Z., ŞIKLAR Z., Berberoǧlu M., Öcal G., ÇETİNKAYA S., et al.

Endocrine Practice , cilt.20, sa.1, ss.46-51, 2014 (SCI-Expanded, Scopus)

140. Kidney growth and renal functions under the growth hormone replacement therapy in children

Ece A., ÇETİNKAYA S., Ekşioǧlu S., ŞENEL S., Özkasap S., Giniş T., et al.

Renal Failure , cilt.36, sa.4, ss.508-513, 2014 (SCI-Expanded, Scopus)

141. Corneal biomechanical characteristics in children with diabetes mellitus

NALÇACIOĞLU MEMİŞ P., Sen E., ÇETİNKAYA S., Bas V., Aycan Z., ÖZTÜRK F.

International Ophthalmology , cilt.34, sa.4, ss.881-886, 2014 (Scopus)

142. Childhood adrenocortical tumors: A single-center experience

Yesil S., ÇETİNKAYA S., Oren A. C., SAVAŞ ERDEVE Ş., Tekgunduz S. A., Candir M. O., et al.

Gazi Medical Journal , cilt.25, sa.4, ss.142-145, 2014 (Scopus, TRDizin)

143. Evaluation of asymmetric dimethylarginine (ADMA) levels in children with growth hormone deficiency

Önder A., Aycan Z., Koca C., Ergin M., ÇETİNKAYA S., Aǧladioǧlu S. Y., et al.

JCRPE Journal of Clinical Research in Pediatric Endocrinology , cilt.6, sa.1, ss.22-27, 2014 (SCI-Expanded, Scopus)

144. The first case of Bruck syndrome associated with gastroschisis

Afşarlar Ç. E., Peltek-Kendirci H. N., ERDOĞAN D., ÖZGÜNER İ. F., ÇAVUŞOĞLU Y. H., KARAMAN A., et al.

Turkish Journal of Pediatrics , cilt.55, sa.6, ss.651-654, 2013 (SCI-Expanded, Scopus)

145. A girl with steroid cell ovarian tumor misdiagnosed as non-classical congenital adrenal hyperplasia

Yilmaz-Aǧladioǧlu S., SAVAŞ ERDEVE Ş., Boduroǧlu E., Önder A., Karaman I., ÇETİNKAYA S., et al.

Turkish Journal of Pediatrics , cilt.55, sa.4, ss.443-446, 2013 (SCI-Expanded, Scopus)

146. Increased central corneal thickness in patients with Turner syndrome

NALÇACIOĞLU MEMİŞ P., Sen E., Onder A., ÇETİNKAYA S., Tos T., KURTUL B. E., et al.

European Journal of Ophthalmology , cilt.24, sa.3, ss.309-313, 2013 (SCI-Expanded, Scopus)

147. Evaluation of bone mineral density in children with type 1 diabetes mellitus

Onder A., ÇETİNKAYA S., Tunc O., Aycan Z.

Journal of Pediatric Endocrinology and Metabolism , cilt.26, sa.11-12, ss.1077-1081, 2013 (SCI-Expanded, Scopus)

148. Common complications in beta-thalassemia patients Beta talasemili hastalarda si{dotless}k görülen komplikasyonlar

Yaman A., Isik P., Yarali N., Karademir S., ÇETİNKAYA S., Bay A., et al.

UHOD - Uluslararasi Hematoloji-Onkoloji Dergisi , cilt.23, sa.3, ss.193-199, 2013 (SCI-Expanded, Scopus, TRDizin)

149. Report of the first case of precocious puberty in Rett syndrome

Baş V. N., ÇETİNKAYA S., Aǧladioǧlu S. Y., Aksoy A., Gülpinar B., Aycan Z.

Journal of Pediatric Endocrinology and Metabolism , cilt.26, sa.9-10, ss.937-939, 2013 (SCI-Expanded, Scopus)

150. Diabetes mellitus with Laron syndrome: Case report

Agladioglu S. Y., ÇETİNKAYA S., SAVAŞ ERDEVE Ş., Onder A., Kendirci H. N. P., Bas V. N., et al.

Journal of Pediatric Endocrinology and Metabolism , cilt.26, sa.9-10, ss.955-958, 2013 (SCI-Expanded, Scopus)

151. Hyperinsulinemic hypoglycemia: Experience in a series of 17 cases

Yilmaz Ag̀ladiog̀lu S., SAVAŞ ERDEVE Ş., ÇETİNKAYA S., Nijat Baş V., Peltek Kendirci H. N., Önder A., et al.

JCRPE Journal of Clinical Research in Pediatric Endocrinology , cilt.5, sa.3, ss.150-155, 2013 (Scopus)

152. Long-term follow-up of Cushing's disease: A case report

Veysel Nijat B., Aǧladíoǧlu S. Y., Önder A., Özíşík P., Kendirci H. N. P., ÇETİNKAYA S., et al.

JCRPE Journal of Clinical Research in Pediatric Endocrinology , cilt.5, sa.3, ss.202-205, 2013 (Scopus)

153. Thyroid dyshormonogenesis is mainly caused by TPO mutations in consanguineous community

Cangul H., Aycan Z., Olivera-Nappa A., SAĞLAM H., Schoenmakers N. A., Boelaert K., et al.

Clinical Endocrinology , cilt.79, sa.2, ss.275-281, 2013 (SCI-Expanded, Scopus)

154. Peroxisome proliferator activated receptor (PPAR)-gamma concentrations in childhood obesity

Akyürek N., Aycan Z., ÇETİNKAYA S., Akyürek Ö., Yilmaz Aǧladioǧlu S., Ertan Ü.

Scandinavian Journal of Clinical and Laboratory Investigation , cilt.73, sa.4, ss.355-360, 2013 (SCI-Expanded, Scopus)

155. Prevalence and long-term follow-up outcomes of testicular adrenal rest tumours in children and adolescent males with congenital adrenal hyperplasia

Aycan Z., Baş V. N., ÇETİNKAYA S., Yilmaz Agladioglu S., TİRYAKİ H. T.

Clinical Endocrinology , cilt.78, sa.5, ss.667-672, 2013 (SCI-Expanded, Scopus)

156. Diabetes care, glycemic control, complications, and concomitant autoimmune diseases in children with type 1 diabetes in Turkey: A multicenter study

Şimsek D. G., Aycan Z., Özen S., ÇETİNKAYA S., Kara C., ABALI S., et al.

JCRPE Journal of Clinical Research in Pediatric Endocrinology , cilt.5, sa.1, ss.20-26, 2013 (Scopus)

157. Value of pelvic sonography in the diagnosis of various forms of precocious puberty in girls

Eksioglu A. S., Yilmaz S., ÇETİNKAYA S., Cinar G., Yildiz Y. T., Aycan Z.

Journal of Clinical Ultrasound , cilt.41, sa.2, ss.84-93, 2013 (SCI-Expanded, Scopus)

158. Assessment of the knowledge of diabetes mellitus among school teachers within the scope of the managing diabetes at school program

Önder A., Aycan Z., ÇETİNKAYA S., Bilgili H., Yildirim N., Baş V. N., et al.

JCRPE Journal of Clinical Research in Pediatric Endocrinology , cilt.4, sa.4, ss.199-203, 2012 (Scopus)

159. A rare combination: Congenital adrenal hyperplasia due to 21 hydroxylase deficiency and Turner syndrome

Kendirci H. N. P., Aycan Z., ÇETİNKAYA S., Baş V. N., Aǧladioǧlu S. Y., Önder A.

JCRPE Journal of Clinical Research in Pediatric Endocrinology , cilt.4, sa.4, ss.213-215, 2012 (Scopus)

160. Mild and severe congenital primary hypothyroidism in two patients by thyrotropin receptor ( TSHR ) gene mutation

Baş V. N., Cangul H., Agladioglu S. Y., Kendall M., ÇETİNKAYA S., Maher E. R., et al.

Journal of Pediatric Endocrinology and Metabolism , cilt.25, sa.11-12, ss.1153-1156, 2012 (SCI-Expanded, Scopus)

161. Assessment of the 21-hydroxylase deficiency and the adrenal functions in young females with Turner syndrome

Onder A., Aycan Z., ÇETİNKAYA S., Kendirci H. N. P., Bas V. N., Agladioglu S. Y.

Journal of Pediatric Endocrinology and Metabolism , cilt.25, sa.7-8, ss.681-685, 2012 (SCI-Expanded, Scopus)

162. Seizure due to somatostatin analog discontinuation in a case diagnosed as congenital hyperinsulinism novel mutation

Baş V. N., Özkan M., ZENCİROĞLU A., ÇAVUŞOĞLU Y. H., ÇETİNKAYA S., Aycan Z.

Journal of Pediatric Endocrinology and Metabolism , cilt.25, sa.5-6, ss.553-555, 2012 (SCI-Expanded, Scopus)

163. TSHR is the main causative locus in autosomal recessively inherited thyroid dysgenesis

Cangul H., Aycan Z., SAĞLAM H., Forman J. R., ÇETİNKAYA S., Tarim O., et al.

Journal of Pediatric Endocrinology and Metabolism , cilt.25, sa.5-6, ss.419-426, 2012 (SCI-Expanded, Scopus)

164. 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

BAŞ F., Darendeliler F., Aycan Z., Çetinkaya E., Berberoǧlu M., ŞIKLAR Z., et al.

Hormone Research in Paediatrics , cilt.77, sa.2, ss.85-93, 2012 (SCI-Expanded, Scopus)

165. Iatrogenic Cushing syndrome due to nasal steroid drops

Baş V. N., ÇETİNKAYA S., Aycan Z.

European Journal of Pediatrics , cilt.171, sa.4, ss.735-736, 2012 (SCI-Expanded, Scopus)

166. A pediatric Conn syndrome case

Onder A., Kendirci H. N. P., Bas V. N., Agladioglu S. Y., ÇETİNKAYA S., Aycan Z.

Journal of Pediatric Endocrinology and Metabolism , cilt.25, sa.1-2, ss.203-206, 2012 (SCI-Expanded, Scopus)

167. Early pubertal development in five children born after assisted reproduction tecniques Yardımcı üreme teknikleri ile doǧan beş olguda görülen erken puberte

Kutlu A. O., ÇETİNKAYA S.

Turk Pediatri Arsivi , cilt.47, sa.3, ss.213-215, 2012 (SCI-Expanded, Scopus, TRDizin)

168. Neonatal diabetes mellitus Yenidoǧanda diyabetes mellitus

Aydin M., ZENCİROĞLU A., Aycan Z., ÇETİNKAYA S., Hakan N., OKUMUŞ N., et al.

Turk Pediatri Arsivi , cilt.47, sa.2, ss.137-140, 2012 (SCI-Expanded, Scopus, TRDizin)

169. Problematic eating behaviour in Turkish children aged 12-72 months: Characteristics of mothers and children

ÖRÜN E., ERDİL Z., ÇETİNKAYA S., Tufan N., YALÇIN Ş.

Central European Journal of Public Health , cilt.20, sa.4, ss.257-261, 2012 (Scopus)

170. Vitamin D status and insulin requirements in children and adolescent with type 1 diabetes

Tunc O., ÇETİNKAYA S., Kízílgün M., Aycan Z.

Journal of Pediatric Endocrinology and Metabolism , cilt.24, sa.11-12, ss.1037-1041, 2011 (SCI-Expanded, Scopus)

171. A case of Langerhans cell histiocytosis with thyroid involvement

Baş V. N., ÇETİNKAYA S., Apaydin S., Bozkurt C., ÇAVUŞOĞLU Y. H., Aycan Z.

Journal of Pediatric Endocrinology and Metabolism , cilt.24, sa.11-12, ss.1059-1061, 2011 (SCI-Expanded, Scopus)

172. Alendronate for the treatment of hypercalcaemia due to neonatal subcutaneous fat necrosis

Hakan N., Aydin M., ZENCİROĞLU A., DEMİREL N., OKUMUŞ N., ÇETİNKAYA S., et al.

European Journal of Pediatrics , cilt.170, sa.8, ss.1085-1086, 2011 (SCI-Expanded, Scopus)

173. The effect of glucocorticoid replacement therapy on bone mineral density in children with congenital adrenal hyperplasia

ÇETİNKAYA S., Kara C.

Journal of Pediatric Endocrinology and Metabolism , cilt.24, sa.5-6, ss.265-269, 2011 (SCI-Expanded, Scopus)

174. A new variant of a known mutation in two siblings with permanent neonatal diabetes mellitus

Aycan Z., ÇETİNKAYA S., Oǧuz Ş. S., CEYLANER S.

Journal of Pediatric Endocrinology and Metabolism , cilt.24, sa.5-6, ss.373-375, 2011 (SCI-Expanded, Scopus)

175. Rhabdomyolysis without detectable myoglobulinuria due to severe hypophosphatemia in diabetic ketoacidosis

Kutlu A. O., Kara C., ÇETİNKAYA S.

Pediatric Emergency Care , cilt.27, sa.6, ss.537-538, 2011 (SCI-Expanded, Scopus)

176. Central precocious puberty secondary to adrenocortical carcinoma: Case report Adrenokortikal karsinoma baǧli gelişen santral erken puberte

Baş V. N., ÇETİNKAYA S., Bozkurt C., Arda N., Yilmaz Aǧladioǧlu S., Peltek Kendirci H. N., et al.

Turkiye Klinikleri Pediatri , cilt.20, sa.2, ss.177-181, 2011 (Scopus)

177. Hyperthyroidism in early childhood, diagnosis and follow-up: Two case reports Erken çocuklukta hipertiroidizm, tani ve i̇zlemi: İki olgu sunumu

Uçkun Kitapçi A., ÇETİNKAYA S.

Turkiye Klinikleri Pediatri , cilt.20, sa.1, ss.90-94, 2011 (Scopus)

178. Evaluation of adrenocortical function in 3-7 aged asthmatic children treated with moderate doses of fluticasone propionate: Reliability of dehydroepiandrosterone sulphate (dhea-s) as a screening test

Sahiner U., ÇETİNKAYA S., ÖZMEN S., Arslan Z.

Allergologia et Immunopathologia , cilt.39, sa.3, ss.154-158, 2011 (SCI-Expanded, Scopus)

179. Thiamine-responsive megaloblastic anemia syndrome with atrial standstill: A case report

Aycan Z., Baş V. N., ÇETİNKAYA S., Aǧladioǧlu S. Y., Kendirci H. N. P., Şenocak F.

Journal of Pediatric Hematology/Oncology , cilt.33, sa.2, ss.144-147, 2011 (SCI-Expanded, Scopus)

180. Eight-year follow-up of a girl with McCune-Albright syndrome

Aycan Z., Önder A., ÇETİNKAYA S.

JCRPE Journal of Clinical Research in Pediatric Endocrinology , cilt.3, sa.1, ss.40-42, 2011 (Scopus)

181. Successful treatment of pulmonary arteriovenous malformation and infantile hepatic hemangioendothelioma with alpha-interferon İnfantil hepatik hemanjiyoendotelyoma ve pulmoner arteriyovenöz malformasyonun alfa-interferon ile başarılı biçimde tedavisi

Özdemir S. I., Bozkurt C., ÖRÜN U. A., ŞAHİN G., Yüksek N., ÇETİNKAYA S., et al.

Anadolu Kardiyoloji Dergisi , cilt.11, sa.2, ss.181-183, 2011 (SCI-Expanded, Scopus, TRDizin)

182. Sporadic nonautoimmune neonatal hyperthyroidism due to A623V germline mutation in the thyrotropin receptor gene

Aycan Z., Aǧladioǧlu S. Y., CEYLANER S., ÇETİNKAYA S., Baş V. N., Kendirci H. N. P.

JCRPE Journal of Clinical Research in Pediatric Endocrinology , cilt.2, sa.4, ss.168-172, 2010 (Scopus)

183. Novel TSHR mutations in consanguineous families with congenital nongoitrous hypothyroidism

Cangul H., Morgan N. V., Forman J. R., SAĞLAM H., Aycan Z., Yakut T., et al.

Clinical Endocrinology , cilt.73, sa.5, ss.671-677, 2010 (SCI-Expanded, Scopus)

184. Response to the letter by Drs. Vanden eijnden and martinovici

ÇETİNKAYA S., Kunak B., Kara C., Demirceken F., Yarah N., POLAT E., et al.

Journal of Pediatric Endocrinology and Metabolism , cilt.23, sa.11, ss.1208, 2010 (SCI-Expanded, Scopus)

185. Cord blood thyroid-stimulating hormone and free T4 levels in Turkish neonates: Is iodine deficiency still a continuing problem?

KIŞLAL F. M., ÇETİNKAYA S., Dilmen U., Yaşar H., Teziç T.

Pediatrics International , cilt.52, sa.5, ss.762-768, 2010 (SCI-Expanded, Scopus)

186. Hypothyroidism due to hepatic hemangioendothelioma: A case report

ÇETİNKAYA S., Kendirci H. N. P., Ag̀ladog̀lu S. Y., Baş V. N., Özdemir S., Bozkurt C., et al.

JCRPE Journal of Clinical Research in Pediatric Endocrinology , cilt.2, sa.3, ss.126-130, 2010 (Scopus)

187. Insulin oedema in newly diagnosed type 1 diabetes mellitus

Baş V. N., ÇETİNKAYA S., Aǧladioǧlu S. Y., Kendirci H. N. P., Bilgili H., Yildirim N., et al.

JCRPE Journal of Clinical Research in Pediatric Endocrinology , cilt.2, sa.1, ss.46-48, 2010 (Scopus)

188. A case report of neonatal diabetes due to neonatal hemochromatosis

ÇETİNKAYA S., Kunak B., Kara C., Demirçeken F., Yarali N., POLAT E., et al.

Journal of Pediatric Endocrinology and Metabolism , cilt.23, sa.5, ss.521-524, 2010 (SCI-Expanded, Scopus)

189. Testicular adrenal rest tumor in a patient with 11β-hydroxylase deficient congenital adrenal hyperplasia

BAYHAN G. İ., ÇETİNKAYA S., Çinar H. G., Aycan Z.

Journal of Pediatric Endocrinology and Metabolism , cilt.23, sa.7, ss.729-732, 2010 (SCI-Expanded, Scopus)

190. Hyperparathyroidism secondary to maternal hypoparathyroidism and vitamin D deficiency: An uncommon cause of neonatal respiratory distress

DEMİREL N., Aydin M., ZENCİROĞLU A., OKUMUŞ N., ÇETİNKAYA S., Yildiz Y., et al.

Annals of Tropical Paediatrics , cilt.29, sa.2, ss.149-154, 2009 (SCI-Expanded, Scopus)

191. The cardiac examination and the cardiac murmurs

ÇETİNKAYA S.

Anadolu Kardiyoloji Dergisi , cilt.9, sa.1, ss.35-36, 2009 (SCI-Expanded, Scopus, TRDizin)

192. Kidney growth in children with congenital hypothyroidism

Bülbül M., ÇETİNKAYA S., Ekşioǧlu S., Özkasap S., Giniş T.

Pediatric Nephrology , cilt.24, sa.2, ss.333-340, 2009 (SCI-Expanded, Scopus)

193. A case with homozygote familial hypercholesterolemia treated with LDL apheresis and coronary bypass in adolescence period Adolesan yaşta koroner baypas yapilan ve LDL aferez tedavisi uygulanan homozigot ailevi hiperkolesterolemi olgusu

Altinel E., ÇETİNKAYA S., Kara C., ÖRÜN U. A., Aydin H., Kutsal A.

Anadolu Kardiyoloji Dergisi , cilt.8, sa.3, ss.231-232, 2008 (Scopus, TRDizin)

194. The effects of metabolic control on oxidized low-density lipoprotein antibodies in children and adolescents with type 1 diabetes mellitus

Kara C., ÇETİNKAYA S., Sezgin N., Kinik S. T.

Pediatric Diabetes , cilt.9, sa.1, ss.17-22, 2008 (SCI-Expanded, Scopus)

195. Diagnostic value of salivary cortisol in children with abnormal adrenal cortex functions

ÇETİNKAYA S., Ozon A., Yordam N.

Hormone Research , cilt.67, sa.6, ss.301-306, 2007 (SCI-Expanded, Scopus)

196. Central diabetes insipidus associated with Caroli syndrome

ÇETİNKAYA S., Alikasifoglu A.

Indian Journal of Pediatrics , cilt.74, sa.4, ss.419-420, 2007 (Scopus)

197. Inappropriate use of potent topical glucocorticoids in infants

Özön A., ÇETİNKAYA S., Alikasifoglu A., GÖNÇ E. N., Şen Y., Kandemir N.

Journal of Pediatric Endocrinology and Metabolism , cilt.20, sa.2, ss.219-225, 2007 (SCI-Expanded, Scopus)

198. Effect of total attending period on infection episode rate in a child-care center

YALÇIN Ş., Tuǧrul B., ÇETİNKAYA S., ÇAKIR B., Yilmaz A.

Pediatrics International , cilt.46, sa.5, ss.555-560, 2004 (Scopus)

199. A case report of rhizomelic chondrodysplasia punctata with hypospadias Rizomelik kondrodisplazia punktatali bir vakada hipospadias

ÇETİNKAYA S., Sarikayalar F., ÖZÖN Z. A., Balci S.

Cocuk Sagligi ve Hastaliklari Dergisi , cilt.47, sa.4, ss.273-276, 2004 (Scopus)

200. Granulocyte-macrophage-colony-stimulating factor in the treatment of neonatal glossitis due to pseudomonas infection Yenidoǧanda psödomonas glossitinin tedavisinde topikal granülosit-makrofaj-koloni stimülan faktör kullanimi

Seren H. C., Semizel E., ÇETİNKAYA S., Yurdakök M., Tekinalp G.

Cocuk Sagligi ve Hastaliklari Dergisi , cilt.46, sa.4, ss.281-283, 2003 (Scopus)

Yayınlar & Eserler