Melike Ersoy

6PUBLICATIONS
45CO-AUTHORS
Gene expression (incl. microarray and other genome-wide approaches)Infant and child healthCancer geneticsMetabolic medicineCancer therapy (excl. chemotherapy and radiation therapy)
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Publications (6)

|Dec 03, 2025
Rare in Rare: Overlapping Clinical Features in a Patient With Both Gaucher Disease Type 1 and B4GALT-CDG: Expanding the Clinical Spectrum With a Novel Pathogenic Variant.

Melike Ersoy, Eda Çelebi Bitkin, Esra Deniz Papatya Çakır

|Jul 21, 2025
Expert opinion on clinical presentation, diagnosis, and treatment of infantile-onset Pompe disease: a Delphi study in Türkiye.

Ekin Özsaydi Aktaşoğlu, Aslı Inci, Rıdvan Murat Öktem

|Oct 08, 2024
In Response to: “Involvement of the Endocrine System is Common in Mitochondrial Disorders and Requires Long-term Comprehensive Investigations”

Esra Deniz Papatya Çakır, Melike Ersoy, Nihan Çakır Biçer

|Aug 08, 2024
Endocrine Disorders in Children with Primary Mitochondrial Diseases: Single Center Experience

Esra Deniz Papatya Çakır, Melike Ersoy, Nihan Çakır Biçer

|Mar 04, 2022
Evaluation of endocrinological involvement and metabolic status in patients with Gaucher disease Type 1 and Fabry disease under enzyme replacement therapy.

Melike Ersoy, Hamide Pişkinpaşa

|Feb 05, 2022
Cobalamin E disease with a novel homozygous MTRR mutation as a cobalamin-related remethylation disorder: a treatable etiology in West syndrome.

Tuğçe Aksu Uzunhan, Bülent Uyanık, Melike Ersoy

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Frequent Collaborators

2 joint publications

Esra Deniz Papatya Çakır

2 joint publications

Nihan Çakır Biçer

2 joint publications

Asuman Gedikbaşı

1 joint publications

Tuğçe Aksu Uzunhan