Mehmet Kocabey

5PUBLICATIONS
36CO-AUTHORS
Metabolic medicineNgā kaiwhakawhānau me te mātai mate tamariki o te Māori (Māori midwifery and paediatrics)Medical mycologyPredictive and prognostic markersNeurogenetics
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Publications (5)

|Oct 02, 2026
Clinical spectrum and genetic landscape of MTHFR deficiency: a cohort study including novel variants.

|Aug 26, 2026
The First Case Series of Malattia Leventinese/Doyne Honeycomb Retinal Dystrophy in Türkiye Identified with EFEMP1 Gene Mutation.

|Jan 19, 2026
Dyggve-Melchior-Clausen syndrome in three siblings: a unique case series with dual diagnosis of Down syndrome and Hirschsprung disease.

Meryem Halis, Mehmet Kocabey, Fatma Ceren Sarıoğlu

|Feb 19, 2024
Experience with cascade screening: A comprehensive family pedigree analysis of two index patients with Fabry disease.

Pelin Teke Kisa, Burcu Ozturk Hismi, Mehmet Kocabey

|Jun 07, 2023
Genetic evaluation of 50 Turkish patients with neurofibromatosis type 1: 2 years experience of a single center.

Mehmet Kocabey, Hande Özkalaycı, Tufan Çankaya

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Frequent Collaborators

2 joint publications

Pelin Teke Kisa

2 joint publications

Nur Arslan

1 joint publications

Hande Özkalaycı

1 joint publications

Ceren Yılmaz Uzman