Piraye Oflazer

Istanbul, 34390, Turkey

Last Updated: 09/26/2026

Save publications for later

Sign Up

Not sure about your diagnosis?

Check Your Symptoms

Found 34 publications

Bridging past and future: the evolution of genetic diagnosis in FSHD and the role of emerging technologies in a globalized framework.

Bridging past and future: the evolution of genetic diagnosis in FSHD and the role of emerging technologies in a globalized framework.

Journal: Neuromuscular disorders : NMD

Published: February 06, 2026

Myasthenia-Like Presentations Following PD-1 Inhibitors: CD8+ Myositis, Myasthenia, or Both?

Myasthenia-Like Presentations Following PD-1 Inhibitors: CD8+ Myositis, Myasthenia, or Both?

Journal: Cureus

Published: January 28, 2026

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

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

Journal: Clinical genetics

Published: September 11, 2025

Urinary Dysfunction in Myasthenic Syndromes: A Scoping Review of Clinical Features and Treatment-Related Associations.

Urinary Dysfunction in Myasthenic Syndromes: A Scoping Review of Clinical Features and Treatment-Related Associations.

Journal: Muscle & nerve

Published: August 29, 2025

Best practice guidelines on genetic diagnostics of facioscapulohumeral muscular dystrophy: Update of the 2012 guidelines.

Best practice guidelines on genetic diagnostics of facioscapulohumeral muscular dystrophy: Update of the 2012 guidelines.

Journal: Clinical genetics

Published: December 07, 2023

Recurrent de-novo gain-of-function mutation in SPTLC2 confirms dysregulated sphingolipid production to cause juvenile amyotrophic lateral sclerosis.

Recurrent de-novo gain-of-function mutation in SPTLC2 confirms dysregulated sphingolipid production to cause juvenile amyotrophic lateral sclerosis.

Journal: Journal of neurology, neurosurgery, and psychiatry

Published: July 28, 2023

The clinical use of impulse oscillometry in neuromuscular diseases.

The clinical use of impulse oscillometry in neuromuscular diseases.

Journal: Respiratory medicine

Published: May 14, 2022

Clinical and genetic characteristics of Emery-Dreifuss muscular dystrophy patients from Turkey: 30 years longitudinal follow-up study.

Clinical and genetic characteristics of Emery-Dreifuss muscular dystrophy patients from Turkey: 30 years longitudinal follow-up study.

Journal: Neuromuscular disorders : NMD

Published: November 15, 2021

1st FSHD European Trial Network workshop:Working towards trial readiness across Europe.

1st FSHD European Trial Network workshop:Working towards trial readiness across Europe.

Journal: Neuromuscular disorders : NMD

Published: June 25, 2021

Giant cell myositis and myocarditis revisited.

Giant cell myositis and myocarditis revisited.

Journal: Acta myologica : myopathies and cardiomyopathies : official journal of the Mediterranean Society of Myology

Published: October 15, 2020

The Complex Genetic Landscape of Hereditary Ataxias in Turkey and Implications in Clinical Practice.

The Complex Genetic Landscape of Hereditary Ataxias in Turkey and Implications in Clinical Practice.

Journal: Movement disorders : official journal of the Movement Disorder Society

Published: October 13, 2020

Creation and implementation of a European registry for patients with McArdle disease and other muscle glycogenoses (EUROMAC registry).

Creation and implementation of a European registry for patients with McArdle disease and other muscle glycogenoses (EUROMAC registry).

Journal: Orphanet journal of rare diseases

Published: April 21, 2020

Showing 1-12 of 34

Last Updated: 09/26/2026