Prof. Dr. Şenay SAVAŞ ERDEVE

1. 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)

2. Clinical and genetic spectrum of SHOX deficiency: phenotypic heterogeneity and the “Jumping SHOX” phenomenon

Doğan Arı A. B., ARI H., Çakar E. Ş., Solmaz T. M., Taşdelen E., Büyükyılmaz G., et al.

European Journal of Pediatrics , cilt.185, sa.6, 2026 (SCI-Expanded, Scopus)

3. Expanding the Coffin–Siris syndrome spectrum: genetic, dysmorphic, and endocrine findings in eight cases

Kolkiran A., Ataseven Kulalı M., Daşar T., Kablan A., Taşdelen E., Atay G., et al.

European Journal of Pediatrics , cilt.185, sa.3, 2026 (SCI-Expanded, Scopus)

4. 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)

5. ACAN-Related Short Stature and Skeletal Dysplasia: Expanding the Phenotypic and Genotypic Spectrum in a 47 Patient Cohort From Turkey

Kolkiran A., Özdemir B. S., Sezer A., Kulalı M. A., Daşar T., SAVAŞ ERDEVE Ş., et al.

American Journal of Medical Genetics, Part A , 2026 (SCI-Expanded, Scopus)

6. Clinical and Molecular Features of 11 Patients with Different Subtypes of Ehlers-Danlos Syndrome

Doğan Arı A. B., ARI H., Sezer A., AĞIRBAŞLI D., KURNAZ E., SAVAŞ ERDEVE Ş., et al.

Molecular Syndromology , ss.1-15, 2026 (SCI-Expanded, Scopus)

7. Two New Families With TAF13 Variant Presenting With Syndromic 46,XY Disorder of Sex Development: Expanding the Clinical Phenotype

ARI H., Türkyılmaz A., Doğan Arı A. B., Kardeş H., Sezer A., CİMBEK E. A., et al.

American Journal of Medical Genetics, Part A , cilt.197, sa.12, 2025 (SCI-Expanded, Scopus)

8. A Novel Premature Termination Codon Mutation in TRAPPC2 Is Associated with X-Linked Spondyloepiphyseal Dysplasia Tarda

Yasar D., Güleray Lafcı N., Karacan Küçükali G., Araslı Yılmaz A., Özkaya Dönmez B., Yazar B. T., et al.

Molecular Syndromology , cilt.16, sa.5, ss.461-468, 2025 (SCI-Expanded, Scopus)

9. Surgical treatment and somatostatin experience in growth hormone-secreting pituitary macroadenoma due to novel AIP mutation

Karagöz K., Eken E. Ş., Karacan Küçükali G., Emrahoğlu M. E., Düzcan Kilimci D., KESKİN M., et al.

Journal of Pediatric Endocrinology and Metabolism , cilt.38, sa.10, ss.1103-1110, 2025 (SCI-Expanded, Scopus)

10. 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)

11. Four New Patients of HHAT-Related Multiple Congenital Anomalies Syndrome (Nivelon-Nivelon-Mabille Syndrome) and a Comprehensive Literature Review

Arı A. B. D., ARI H., Türkyılmaz A., Teralı K., Büyükyılmaz G., SAVAŞ ERDEVE Ş., et al.

American Journal of Medical Genetics, Part A , cilt.197, sa.9, 2025 (SCI-Expanded, Scopus)

12. DNA ligase IV deficiency identified in a patient with hypergonadotropic hypogonadism: a case report

Yasar D., Sezer A., Aytekin C., Karacan Küçükali G., Özkaya Dönmez B., Arasll Yllmaz A., et al.

Journal of Pediatric Endocrinology and Metabolism , cilt.38, sa.4, ss.415-420, 2025 (SCI-Expanded, Scopus)

13. 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)

14. Natural history of ENPP1 deficiency: Nationwide Turkish Cohort Study of autosomal-recessive hypophosphataemic rickets type 2

DURSUN F., TURAN İ., Bitkin E. Ç., BAYRAMOĞLU E., Çayır A., SAVAŞ ERDEVE Ş., et al.

Clinical Endocrinology , cilt.101, sa.5, ss.475-484, 2024 (SCI-Expanded, Scopus)

15. 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)

16. 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)

17. 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)

18. 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)

19. 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)

20. 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)

21. 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)

22. 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)

23. 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)

24. 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)

25. 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)

26. 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)

27. 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)

28. 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)

29. 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)

30. 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)

31. Decreased vitamin D levels in children and adolescents with Celiac disease: A nationwide cross-sectional study

AKELMA A. Z., KESKİN M., SAVAŞ ERDEVE Ş., BURSA SATICI N., Çelik O., İmrat E., et al.

Gulhane Medical Journal , cilt.64, sa.3, ss.268-273, 2022 (Scopus, TRDizin)

32. 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)

33. 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)

34. 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)

35. Recommendations for Clinical Decision-making in Children with Type 1 Diabetes and Celiac Disease: Type 1 Diabetes and Celiac Disease Joint Working Group Report

Hatun Ş., DALGIÇ B., Gökşen D., Aydoğdu S., SAVAŞ ERDEVE Ş., Kuloğu Z., et al.

JCRPE Journal of Clinical Research in Pediatric Endocrinology , cilt.14, sa.1, ss.1-9, 2022 (SCI-Expanded, Scopus, TRDizin)

36. 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)

37. 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)

38. 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)

39. 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)

40. 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)

41. Thrombocytopenia-Associated Multi-Organ Failure Due to Diabetic Ketoacidosis and Viral Infection: A Case Report

Torun E. G., Yazici M. U., Azapagasi E., SAVAŞ ERDEVE Ş.

Klinische Padiatrie , cilt.233, sa.3, ss.149-151, 2021 (SCI-Expanded, Scopus)

42. 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)

43. 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)

44. 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)

45. 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)

46. 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)

47. 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)

48. Is Bioavailable Vitamin D Better Than Total Vitamin D to Evaluate Vitamin D Status in Obese Children?

Karacan Küçükali G., GÜLBAHAR Ö., Özalkak Ş., Dağlı H., CEYLANER S., Aycan Z., et al.

JCRPE Journal of Clinical Research in Pediatric Endocrinology , cilt.13, sa.4, ss.391-399, 2021 (SCI-Expanded, Scopus, TRDizin)

49. Treatment difficulties in hypomagnesemia secondary to the transient receptor potential melastatin 6 gene: A case report with novel mutation

Yücel H., Sel Ç. G., Kasapkara Ç. S., Küçükali G. K., SAVAŞ ERDEVE Ş., Öztoprak Ü., et al.

JCRPE Journal of Clinical Research in Pediatric Endocrinology , cilt.13, sa.1, ss.114-118, 2021 (SCI-Expanded, Scopus, TRDizin)

50. 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)

51. 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)

52. 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)

53. 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)

54. 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)

55. 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)

56. 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)

57. 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)

58. 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)

59. Contribution of functionally assessed GHRHR mutations to idiopathic isolated growth hormone deficiency in patients without GH1 mutations

Cohen E., Belkacem S., Fedala S., Collot N., Khallouf E., Dastot F., et al.

Human Mutation , cilt.40, sa.11, ss.2033-2043, 2019 (SCI-Expanded, Scopus)

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

Hatun S., Yesiltepe Mutlu G., Cinaz P., DEMİRCİOĞLU S., Ekberzade A., BEREKET A., et al.

Diabetic Medicine , cilt.36, sa.10, ss.1243-1250, 2019 (SCI-Expanded, Scopus)

61. 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)

62. 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)

63. 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)

64. 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)

65. 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)

66. 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)

67. 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)

68. 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)

69. 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)

70. 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)

71. 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)

72. 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)

73. 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)

74. 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)

75. 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)

76. 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)

77. 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)

78. 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)

79. 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)

80. 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)

81. Clinical presentations, metabolic abnormalities and end-organ complications in patients with familial partial lipodystrophy

Akinci B., Onay H., Demir T., SAVAŞ ERDEVE Ş., Gen R., Simsir I. Y., et al.

Metabolism: Clinical and Experimental , cilt.72, ss.109-119, 2017 (SCI-Expanded, Scopus)

82. 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)

83. 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)

84. 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)

85. A child with Laron syndrome associated with vasculitis

SAÇ R., TAŞAR M. A., Tiras U., SAVAŞ ERDEVE Ş., Bilge Y. D.

Acta Endocrinologica , cilt.12, sa.4, ss.465-468, 2016 (SCI-Expanded, Scopus)

86. 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)

87. 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)

88. Is chromosomal study necessary for girls with inguinal hernia?

KURNAZ E., SAVAŞ ERDEVE Ş., Aycan Z.

Journal of Clinical and Diagnostic Research , cilt.10, sa.8, 2016 (Scopus)

89. 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)

90. Gonadotropin-releasing hormone analogue treatment in females with moderately early puberty: No effect on final height

SAVAŞ ERDEVE Ş., ŞIKLAR Z., Hacıhamdioğlu B., Kocaay P., ÇAMTOSUN E., Öcal G., et al.

JCRPE Journal of Clinical Research in Pediatric Endocrinology , cilt.8, sa.2, ss.211-217, 2016 (SCI-Expanded, Scopus, TRDizin)

91. 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)

92. Co-existence of thyroid nodule and thyroid cancer in children and adolescents with hashimoto thyroiditis: A single-center study

KESKİN M., SAVAŞ ERDEVE Ş., Aycan Z.

Hormone Research in Paediatrics , cilt.85, sa.3, ss.181-187, 2016 (SCI-Expanded, Scopus)

93. 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)

94. 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)

95. 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)

96. The effect of recombinant growth hormone treatment in children with idiopathic short stature and low insulin-like growth factor-1 levels

ŞIKLAR Z., Kocaay P., ÇAMTOSUN E., İsakoca M., Hacıhamdioğlu B., SAVAŞ ERDEVE Ş., et al.

JCRPE Journal of Clinical Research in Pediatric Endocrinology , cilt.7, sa.4, ss.301-306, 2015 (SCI-Expanded, Scopus, TRDizin)

97. Investigation of androgen receptor gene mutations in a series of 21 patients with 46,XY disorders of sex development

Topcu V., Ilgin-Ruhi H., ŞIKLAR Z., KARABULUT H. G., Berberoglu M., Hacihamdioglu B., et al.

Journal of Pediatric Endocrinology and Metabolism , cilt.28, sa.11-12, ss.1257-1263, 2015 (SCI-Expanded, Scopus)

98. Rett syndrome and precocious puberty association

KESKİN M., SAVAŞ ERDEVE Ş., Aycan Z.

Journal of Pediatric Endocrinology and Metabolism , cilt.28, sa.9-10, ss.1197, 2015 (SCI-Expanded, Scopus)

99. 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)

100. 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)

101. 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)

102. Clinical review of 95 patients with 46,xx disorders of sex development based on the new chicago classification

Öcal G., Berberoğlu M., ŞIKLAR Z., Aycan Z., Hacihamdioglu B., SAVAŞ ERDEVE Ş., et al.

Journal of Pediatric and Adolescent Gynecology , cilt.28, sa.1, ss.6-11, 2015 (SCI-Expanded, Scopus)

103. 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)

104. The evaluation of thyroid carcinoma in childhood and concomitance of autoimmune thyroid disorders

HacIhamdioʇlu B., Öçal G., Berberoʇlu M., SAVAŞ ERDEVE Ş., ÇAMTOSUN E., Kocaay P., et al.

Journal of Pediatric Endocrinology and Metabolism , cilt.27, sa.9-10, ss.901-908, 2014 (SCI-Expanded, Scopus)

105. Preperitoneal fat tissue may be associated with arterial stiffness in obese adolescents

Hacihamdioǧlu B., Öçal G., Berberoǧlu M., ŞIKLAR Z., FİTOZ Ö. S., Tutar E., et al.

Ultrasound in Medicine and Biology , cilt.40, sa.5, ss.871-876, 2014 (SCI-Expanded, Scopus)

106. 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)

107. 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)

108. 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)

109. 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)

110. Pathophysiology of critical illness hyperglycemia in children

Hacihamdioǧlu B., KENDİRLİ T., Öçal G., ŞIKLAR Z., SAVAŞ ERDEVE Ş., Ince E., et al.

Journal of Pediatric Endocrinology and Metabolism , cilt.26, sa.7-8, ss.715-720, 2013 (SCI-Expanded, Scopus)

111. Relationships between osteocalcin, glucose metabolism, and adiponectin in obese children: Is there crosstalk between bone tissue and glucose metabolism?

Abseyi N., ŞIKLAR Z., Berberoǧlu M., Hacihamdioǧlu B., SAVAŞ ERDEVE Ş., Öçal G.

JCRPE Journal of Clinical Research in Pediatric Endocrinology , cilt.4, sa.4, ss.182-188, 2012 (Scopus)

112. The clinical and genetic heterogeneity of mixed gonadal dysgenesis: Does "disorders of sexual development (DSD)" classification based on new Chicago consensus cover all sex chromosome DSD?

Öcal G., Berberoǧlu M., ŞIKLAR Z., Ruhi H. I., Tükün A., ÇAMTOSUN E., et al.

European Journal of Pediatrics , cilt.171, sa.10, ss.1497-1502, 2012 (SCI-Expanded, Scopus)

113. Synchronous occurrence of papillary carcinoma in the thyroid gland and thyroglossal duct in an adolescent with congenital hypothyroidism

ŞIKLAR Z., Berberoǧlu M., Yaǧmurlu A., Hacihamdioǧlu B., SAVAŞ ERDEVE Ş., FİTOZ Ö. S., et al.

JCRPE Journal of Clinical Research in Pediatric Endocrinology , cilt.4, sa.1, ss.30-33, 2012 (Scopus)

114. Characteristics and prevalence of non-classical congenital adrenal hyperplasia with a V281l mutation in patients with premature pubarche

SAVAŞ ERDEVE Ş., Berberoglu M., Yurur-Kutlay N., ŞIKLAR Z., Hacíhamdíoglu B., Tukun A., et al.

Journal of Pediatric Endocrinology and Metabolism , cilt.24, sa.11-12, ss.965-970, 2011 (SCI-Expanded, Scopus)

115. The endocrine spectrum of intracranial cysts in childhood and review of the literature

SAVAŞ ERDEVE Ş., Ocal G., Berberoglu M., ŞIKLAR Z., Hacihamdioglu B., EVLİYAOĞLU S. O., et al.

Journal of Pediatric Endocrinology and Metabolism , cilt.24, sa.11-12, ss.867-875, 2011 (SCI-Expanded, Scopus)

116. Transient neonatal diabetes with two novel mutations in the KCNJ11 gene and response to sulfonylurea treatment in a preterm infant

ŞIKLAR Z., Ellard S., OKULU E., Berberoǧlu M., Young E., SAVAŞ ERDEVE Ş., et al.

Journal of Pediatric Endocrinology and Metabolism , cilt.24, sa.11-12, ss.1077-1080, 2011 (SCI-Expanded, Scopus)

117. Clinical characteristics of recessive and dominant congenital hyperinsulinism due to mutation(s) in the ABCC8/KCNJ11 genes encoding the ATP-sensitive potasium channel in the pancreatic beta cell

Öçal G., Flanagan S. E., Hacihamdioǧlu B., Berberoǧlu M., ŞIKLAR Z., Ellard S., et al.

Journal of Pediatric Endocrinology and Metabolism , cilt.24, sa.11-12, ss.1019-1023, 2011 (SCI-Expanded, Scopus)

118. Evaluation of hypercoagulability in obese children with thrombin generation test and microparticle release: Effect of metabolic parameters

ŞIKLAR Z., Öçal G., Berberoǧlu M., Hacihamdioǧlu B., SAVAŞ ERDEVE Ş., Eǧin Y., et al.

Clinical and Applied Thrombosis/Hemostasis , cilt.17, sa.6, ss.585-589, 2011 (SCI-Expanded, Scopus)

119. Primary adrenal insufficiency in a child after busulfan and cyclophosphamide-based conditioning for hematopoietic stem cell transplantation

SAVAŞ ERDEVE Ş., Berberoglu M., ŞIKLAR Z., Hacihamdioglu B., Ocal G., ERTEM M., et al.

Journal of Pediatric Endocrinology and Metabolism , cilt.24, sa.9-10, ss.853-855, 2011 (SCI-Expanded, Scopus)

120. Efficiency of fluid treatments with different sodium concentration in children with type 1 diabetic ketoacidosis

SAVAŞ ERDEVE Ş., Berberoǧlu M., Oygar P., ŞIKLAR Z., KENDİRLİ T., Hacihamdioǧlu B., et al.

JCRPE Journal of Clinical Research in Pediatric Endocrinology , cilt.3, sa.3, ss.149-153, 2011 (Scopus)

121. Neonatal urticaria due to topical mupirocin Topikal mupirosine baǧli̇ yenidoǧan ürtikeri

ERDEVE Ö., SAVAŞ ERDEVE Ş., Sarici Ü. S.

Erciyes Tip Dergisi , cilt.33, sa.2, ss.149-152, 2011 (Scopus, TRDizin)

122. Is adrenocorticotropic hormone deficiency really rare in patients with idiopathic growth hormone deficiency and normal thyroid function tests?

SAVAŞ ERDEVE Ş., Ocal G., Berberoglu M., ŞIKLAR Z., Hacihamdioglu B.

Hormone Research in Paediatrics , cilt.75, sa.3, ss.200-205, 2011 (SCI-Expanded, Scopus)

123. Contribution of clinical, metabolic, and genetic factors on hypertension in obese children and adolescents

ŞIKLAR Z., Berberoglu M., SAVAŞ ERDEVE Ş., Hacihamdioglu B., Öcal G., Egin Y., et al.

Journal of Pediatric Endocrinology and Metabolism , cilt.24, sa.1-2, ss.21-24, 2011 (SCI-Expanded, Scopus)

124. Two siblings with isolated GH deficiency due to loss-of-function mutation in the GHRHR gene: Successful treatment with growth hormone despite late admission and severe growth retardation

ŞIKLAR Z., Berberoǧlu M., Legendre M., Amselem S., EVLİYAOĞLU S. O., Hacihamdioǧlu B., et al.

JCRPE Journal of Clinical Research in Pediatric Endocrinology , cilt.2, sa.4, ss.164-167, 2010 (Scopus)

125. Utility of apoB/apoA1 ratio for the prediction of cardiovascular risk in childrenwith metabolic syndrome

SAVAŞ ERDEVE Ş., ŞİMŞEK E., Dallar Y., Biyikli Z.

Indian Journal of Pediatrics , cilt.77, sa.11, ss.1261-1265, 2010 (SCI-Expanded, Scopus)

126. Familial clustering of metabolic syndrome components in parents of obese children

SAVAŞ ERDEVE Ş., Simsek E., Dallar Y., Biyikli Z.

Endocrinologist , cilt.20, sa.5, ss.240-242, 2010 (SCI-Expanded, Scopus)

127. Genoa syndrome and central diabetes insipidus: A case report

Hacihamdioǧlu B., ŞIKLAR Z., SAVAŞ ERDEVE Ş., Berberoǧlu M., Deda G., Tiraş S. T., et al.

JCRPE Journal of Clinical Research in Pediatric Endocrinology , cilt.2, sa.2, ss.89-91, 2010 (Scopus)

128. Long-term follow-up of a pseudohypoparathyroidism type 1a patient with missense mutation (pro115ser) in exon 5

SAVAŞ ERDEVE Ş., Berberoǧlu M., ŞIKLAR Z., EVLİYAOĞLU S. O., Hiort O., Öcal G.

JCRPE Journal of Clinical Research in Pediatric Endocrinology , cilt.2, sa.2, ss.85-88, 2010 (Scopus)

129. A novel mutation of 5α-steroid reductase 2 deficiency (CD 65 ALA-PRO) with severe virilization defect in a Turkish family and difficulty in gender assignment

SAVAŞ ERDEVE Ş., Aycan Z., Berberoglu M., ŞIKLAR Z., Hacıhamdıoglu B., Sıpahı K., et al.

European Journal of Pediatrics , cilt.169, sa.8, ss.991-995, 2010 (SCI-Expanded, Scopus)

130. Amiodarone-induced thyrotoxicosis in children and adolescents is a possible outcome in patients with low iodine intake

Hacihamdioǧlu B., Berberoǧlu M., ŞIKLAR Z., SAVAŞ ERDEVE Ş., Öçal G., Tutar E., et al.

Journal of Pediatric Endocrinology and Metabolism , cilt.23, sa.4, ss.363-368, 2010 (SCI-Expanded, Scopus)

131. Efficacy and safety of Saccharomyces boulardii in amebiasis-associated diarrhea in children

SAVAŞ ERDEVE Ş., Gökay S., Dallar Y.

Turkish Journal of Pediatrics , cilt.51, sa.3, ss.220-224, 2009 (SCI-Expanded, Scopus)

132. Evaluation of final height and parentally adjusted height deficit in isolated growth hormone deficient children with or without short parents

ŞIKLAR Z., Berberoǧlu M., Öçal G., BİLİR P., SAVAŞ ERDEVE Ş.

Endocrinologist , cilt.19, sa.6, ss.285-287, 2009 (SCI-Expanded, Scopus)

133. Pituitary hyperplasia mimicking pituitary macroadenoma in two adolescent patients with long-standing primary hypothyroidism: Case reports and review of literature

Şimşek E., ŞİMŞEK T., SAVAŞ ERDEVE Ş., Erdoǧmuş B., Döşoǧlu M.

Turkish Journal of Pediatrics , cilt.51, sa.6, ss.624-630, 2009 (SCI-Expanded, Scopus)

134. A novel mutation of the GLUT2 gene in a Turkish patient with Fanconi-Bickel syndrome

Şimşek E., SAVAŞ ERDEVE Ş., Sakamoto O., Doǧanci T., Dallar Y.

Turkish Journal of Pediatrics , cilt.51, sa.2, ss.166-168, 2009 (SCI-Expanded, Scopus)

135. Harlequin ichthyosis: A case report Harlequin iktiyozis: Bir olgu sunumu

SAVAŞ ERDEVE Ş., Türkoǧlu Ö., Can Ö., ASTARCI H. M., Tiraş Ü.

Gulhane Medical Journal , cilt.49, sa.1, ss.52-54, 2007 (Scopus, TRDizin)

136. Serum sialic acid, hs-CRP and oxidative stress parameters in obese children

Yilmaz F. M., YILMAZ G., SAVAŞ ERDEVE Ş., Dallar Y., Topkaya B., YÜCEL D.

Journal of Pediatric Endocrinology and Metabolism , cilt.20, sa.2, ss.205-210, 2007 (SCI-Expanded, Scopus)

137. Testicular microlithiasis and McCune-Albright syndrome

SAVAŞ ERDEVE Ş., Balta H., Balta Z., Dallar Y.

Journal of Pediatrics , cilt.148, sa.3, ss.422, 2006 (SCI-Expanded, Scopus)

138. Does obesity lead to depression and self-esteem deficiency in children? Obezite, çocuklarda depresyon ve özgüven eksikliǧine neden oluyor mu?

Dallar Y., SAVAŞ ERDEVE Ş., Çakir I., Köstü M.

Gulhane Medical Journal , cilt.48, sa.1, ss.1-3, 2006 (Scopus, TRDizin)

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