Shahram Attarian
Marseille, France
Last Updated: 09/26/2026
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Found 274 publications
Myopathies in the therapeutic era: measurement as the rate-limiting step.
Journal: Current opinion in neurology
Published: September 03, 2026
Biomarkers in facioscapulohumeral muscular dystrophy.
Journal: Current opinion in neurology
Published: August 22, 2026
Tofersen Treatment in SOD1-ALS: Real-World Evidence from a Retrospective Multicenter Study in France (FORSLA Study).
Journal: Mayo Clinic proceedings. Innovations, quality & outcomes
Published: August 04, 2026
High risk of hypoxemic COVID-19 pneumonia in myasthenia gravis patients with type I IFN autoantibodies.
Journal: Proceedings of the National Academy of Sciences of the United States of America
Published: July 31, 2026
2025 update of the National French consensus on gene lists for the diagnosis of muscle diseases using high-throughput sequencing.
Journal: Journal of neuromuscular diseases
Published: July 09, 2026
Restoring the interplay between the endoplasmic reticulum and mitochondria by gene therapy improves Charcot-Marie-Tooth type 2A disease.
Journal: Proceedings of the National Academy of Sciences of the United States of America
Published: June 16, 2026
Corrigendum to 'Diagnostic adjudication of potential participants with chronic inflammatory demyelinating polyradiculoneuropathy in the ADHERE trial of subcutaneous efgartigimod PH20' [Journal of the Neurological Sciences, 486 (2026) 125918].
Journal: Journal of the neurological sciences
Published: May 13, 2026
High risk of hypoxemic COVID-19 pneumonia in myasthenia gravis patients with type I IFN autoantibodies.
Journal: medRxiv : the preprint server for health sciences
Published: April 10, 2026
Real-world effectiveness and safety of zilucoplan in patients with anti-AChR myasthenia gravis: A retrospective cohort study in France.
Journal: Journal of neuromuscular diseases
Published: March 29, 2026
Clinical effectiveness of efgartigimod in a broad population of patients with generalized myasthenia gravis: subgroup analyses from a randomized, double‑blind, placebo‑controlled, phase 3 trial (ADAPT).
Journal: Journal of neurology
Published: February 22, 2026
Clinical Features and Prognosis of SEPTIN9-Related Hereditary Neuralgic Amyotrophy.
Journal: European journal of neurology
Published: January 29, 2026
Last Updated: 09/26/2026