Melikşah Keskın

Ministry of Health — Turkey

Biochemistry, Genetics and Molecular Biology · Life Sciences

12h-index387citations91works0.42yr avg
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Research Topics

Sexual Differentiation and Disorders(13), Ovarian function and disorders(10), Vitamin D Research Studies(7), Parathyroid Disorders and Treatments(6), Thyroid Disorders and Treatments(5)

Publications91 total

Is the tracheal index useful for evaluating the thyroid in infants suspected of hypothyroidism?
Journal of Pediatric Endocrinology and Metabolism·2025
Surgical treatment and somatostatin experience in growth hormone-secreting pituitary macroadenoma due to novel <i>AIP</i> mutation
Journal of Pediatric Endocrinology and Metabolism·2025
Paediatric drug-induced epidermal necrolysis: insights from real-world evidence in Türkiye
Clinical and Experimental Dermatology·2025· 1 cited
Evaluation of emergency department admission reasons and associated factors in pediatric patients diagnosed with type 1 diabetes mellitus
Endocrine Abstracts·2025
Pediatric parathyroid adenomas: a single tertiary care center experience
Endocrine Abstracts·2025
Clinical follow-up data of patients diagnosed with obesity
Endocrine Abstracts·2025
A case of autonomous hot thyroid nodule
Endocrine Abstracts·2025
A case of leydig cell tumor presenting with peripheral precocious puberty
Endocrine Abstracts·2025
Evaluation of test results according to body mass index of patients who had a gnrh stimulation test with a preliminary diagnosis of precocious puberty
Endocrine Abstracts·2025
Evaluation of the effects of antithyroid drug therapy on body mass index in children and adolescents with graves' disease
Endocrine Abstracts·2025
DNA ligase IV deficiency identified in a patient with hypergonadotropic hypogonadism: a case report
Journal of Pediatric Endocrinology and Metabolism·2025
Changes in anaphylaxis trends and characteristics in emergency department admissions in Türkiye: From 2015 to 2021 based on the Ministry of Health database
World Allergy Organization Journal·2024Open Access
A Novel Premature Termination Codon Mutation in TRAPPC2 Is Associated with X-Linked Spondyloepiphyseal Dysplasia Tarda
Molecular Syndromology·2024Open Access
Santral Puberte Prekoks Tanılı Kızlarda GNRH Analog Tedavisinin Antropometrik Ölçüm Değerlerine etkisi: Bir Yıllık Takip Sonuçları
OSMANGAZİ JOURNAL OF MEDICINE·2024Open Access
Clinical and Laboratory Characteristics of MODY (Maturity Onset Diabetes of Young) Cases, Genetic Mutation Spectrum and Phenotype-genotype Relationship
Journal of Clinical Research in Pediatric Endocrinology·2024· 6 citedOpen Access
EVALUATION OF FINAL HEIGHT IN PATIENTS WITH CONGENITAL ADRENAL HYPERPLASIA
Pamukkale Medical Journal·2024Open Access
3M syndrome: Evaluating the clinical and laboratory features and the response of the growth hormone treatment: Single center experience
European Journal of Medical Genetics·2023· 10 cited
Genotype of congenital adrenal hyperplasia patients with testicular adrenal rest tumor
European Journal of Medical Genetics·2022· 6 citedOpen Access
Decreased vitamin D levels in children and adolescents with Celiac disease: A nationwide cross-sectional study
Gulhane Medical Journal·2022· 5 citedOpen Access
Status of Central Precocious Puberty Cases at the Onset of Coronavirus Disease 2019 Pandemic: A Single-Center Experience
Turkish Archives of Pediatrics·2022· 9 citedOpen Access
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Frequent Co-authors

Zehra Aycan(35), Semra Çeti̇nkaya(34), Şenay Savaş Erdeve(33), Erdal Kurnaz(17), Elif Sağsak(14), Nursel Muratoğlu Şahin(10), Elvan Bayramoğlu(8), Erdeve Şenay Savaş(5), Gülin Karacan Küçükali(3), Corinne Magdelaine(2), Anne Lienhardt-Roussie(2), Tülay Güran(2), Ufuk Elgin(2), Senem Esen(2), Ayşe Karaman(2), Sema Apaydın(2), Nihal Hatipoğlu(2), Firdevs Baş(2), Şervan Özalkak(2), Nesibe Akyürek(2)