Eda Mengen Uçaktürk

20PUBLICATIONS
105CO-AUTHORS
Developmental genetics (incl. sex determination)Polymerisation mechanismsInfant and child healthMedical devicesNeonatology
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Publications (20)

|Jun 12, 2026
<i>AR</i> gene functional domains and their role in clinical severity in androgen insensitivity syndrome: a single-center cohort from Turkey.

|Oct 16, 2025
Phosphoglucomutase 1 deficiency misdiagnosed as Laron syndrome.

Seyit Ahmet Uçaktürk, Emre Özer, Ahmet Cevdet Ceylan

|Jun 27, 2025
Urinary plasminogen as an early marker of diabetic kidney disease in children with type 1 diabetes mellitus: a cross-sectional study.

Mihriban İnözü, Gönül Büyükyılmaz, Begüm Avcı

|Jun 19, 2025
A novel homozygous missense <i>DNAJC3</i> variant in syndromic juvenile-onset diabetes.

Eda Mengen, Deniz Kor, Fatma Derya Bulut

|May 23, 2025
The First-Year Outcomes of the Nationwide Neonatal CAH Screening in Türkiye: High Rate of False Positives for 21-Hydroxylase Deficiency and a Higher Detection Rate of Non-Classical Cases

Tülay Güran, Elif Yürüker, Ahmet Anık

|Mar 08, 2025
Optimal timing of repeat thyroid fine-needle aspiration biopsy.

Mevra Cay, Ihsan Turan, Eda Mengen

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Frequent Collaborators

11 joint publications

Seyit Ahmet Uçaktürk

5 joint publications

İhsan Turan

4 joint publications

Pınar Kocaay

3 joint publications

Bilgin Yüksel