Doç. Dr. Melikşah KESKİN

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. 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)

3. 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)

4. 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)

5. 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)

6. 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)

7. 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)

8. 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)

9. 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)

10. 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)

11. 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)

12. Is idiopathic mild hyperprolactinemia a cardiovascular risk factor?

OR KOCA A., Daǧdeviren M., AKKAN T., KESKİN M., Pamuk N., ALTAY M.

Nigerian Journal of Clinical Practice , cilt.24, sa.2, ss.213-219, 2021 (SCI-Expanded, Scopus)

13. 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)

14. 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)

15. 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)

16. Early visual field changes in patients with type 1 diabetes mellitus

Ozates S., Simsek M., Elgin U., KESKİN M., Aycan Z.

European Journal of Ophthalmology , cilt.30, sa.6, ss.1467-1472, 2020 (SCI-Expanded, Scopus)

17. 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)

18. 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)

19. 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)

20. 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)

21. 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)

22. 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)

23. 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)

24. 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)

25. 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)

26. 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)

27. 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)

28. 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)

29. 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)

30. 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)

31. 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)

32. 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)

33. 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)

34. 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)

35. 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)

36. 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)

37. 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)

38. 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)

39. 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)

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