Zehra Piraye Oflazer

5PUBLICATIONS
53CO-AUTHORS
Neurology and neuromuscular diseasesGene expression (incl. microarray and other genome-wide approaches)Prosthetics and orthotics
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Publications (5)

|Aug 04, 2026
Hereditary Polyneuropathy Experience of a Tertiary Single-Center in Türkiye: Beyond the Tip of the Iceberg.

|Dec 26, 2025
Congenital Myasthenic Syndrome: Long-Term Outcomes up to 60 Years, Molecular Characterization, and Eight Novel Variants.

Ayfer Arduç Akçay, Gulshan Yunisova, Şahin Avcı

|Apr 29, 2024
Best practice guidelines on genetic diagnostics of facioscapulohumeral muscular dystrophy: Update of the 2012 guidelines.

Emiliano Giardina, Pilar Camaño, Sarah Burton-Jones

|Feb 27, 2024
SNUPN deficiency causes a recessive muscular dystrophy due to RNA mis-splicing and ECM dysregulation.

Marwan Nashabat, Nasrinsadat Nabavizadeh, Hilal Pırıl Saraçoğlu

|Oct 29, 2019
Functional Outcomes and Complications Following Scapulothoracic Arthrodesis in Patients with Facioscapulohumeral Dystrophy.

İlker Eren, Ali Erşen, Olgar Birsel

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Frequent Collaborators

2 joint publications

Hülya Kayserili

2 joint publications

Ayşe Nur Özdağ Acarlı

2 joint publications

Şahin Avcı

2 joint publications

Ayfer Arduç Akçay