Meliha Demiral

14PUBLICATIONS
42CO-AUTHORS
Adolescent healthNeonatologyGene expression (incl. microarray and other genome-wide approaches)Cardiology (incl. cardiovascular diseases)Gene mapping
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Publications (14)

|Jun 19, 2023
Early puberty paradox: an investigation of anxiety levels of mothers and children, children's quality of life, and psychiatric diagnoses.

Burcu Kardaş, Ömer Kardaş, Meliha Demiral

|Jan 02, 2023
Elevated amylase and lipase levels in patients with DKA followed in the pediatric intensive care unit.

Gulhan Atakul, Meliha Demiral, Güliz Gürer

|Jun 23, 2022
Metreleptin Treatment in a Boy with Congenital Generalized Lipodystrophy due to Homozygous c.465_468delGACT (p.T156Rfs*8) Mutation in the BSCL2 Gene: Results From the First-year

Şervan Özalkak, Meliha Demiral, Edip Ünal

|Dec 30, 2020
Clinical Characteristics of 46,XX Males with Congenital Adrenal Hyperplasia

Şenay Savaş-Erdeve, Zehra Aycan, Semra Çetinkaya

|Oct 30, 2020
Cytochrome P450 oxidoreductase deficiency caused by a novel mutation in the POR gene in two siblings: case report and literature review.

Edip Unal, Meliha Demiral, Ruken Yıldırım

|Sep 17, 2020
Identification of Three Novel and One Known Mutation in the WFS1 Gene in Four Unrelated Turkish Families: The Role of Homozygosity Mapping in the Early Diagnosis

Maha Sherif, Hüseyin Demirbilek, Atilla Çayır

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Frequent Collaborators

9 joint publications

Mehmet Nuri Özbek

8 joint publications

Hüseyin Demirbilek

8 joint publications

Edip Unal

2 joint publications

Serdar Ceylaner