Bruno Eymard
Centre De Référence De Pathologie Neuromusculaire Paris Est
Estonia
Estonia
Last Updated: 09/26/2026
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Found 181 publications
Relative frequencies of muscle specific kinase antibody myasthenia in 46 centres worldwide.
Journal: Brain : a journal of neurology
Published: February 11, 2026
Unveiling MYH2-related myopathy: Histological-genetic insights from a case series and systematic review.
Journal: Journal of neuromuscular diseases
Published: November 18, 2025
Limb Girdle Muscular Dystrophy Associated With TRIM32 Variants: A National Cohort Study.
Journal: Muscle & nerve
Published: September 08, 2025
C-terminal extension of HSPB6 in a family with myopathy and cataract.
Journal: Human molecular genetics
Published: April 25, 2025
Disease Trajectories of a Large French Cohort of 142 Congenital Myopathy Patients in Adult Age.
Journal: European journal of neurology
Published: October 16, 2024
Comparison of juvenile and adult myasthenia gravis in a French cohort with focus on thymic histology.
Journal: Scientific reports
Published: February 02, 2024
Congenital myasthenic syndromes in adults: clinical features, diagnosis and long-term prognosis.
Journal: Brain : a journal of neurology
Published: December 09, 2023
Congenital myasthenic syndromes with kinetic abnormalities of the acetylcholine receptor
Journal: Medecine sciences : M/S
Published: November 17, 2023
Molecular Analysis of a Congenital Myasthenic Syndrome Due to a Pathogenic Variant Affecting the C-Terminus of ColQ.
Journal: International journal of molecular sciences
Published: September 29, 2023
Innovative Therapeutic Approaches in Congenital Myasthenic Syndromes.
Journal: Neurology. Clinical practice
Published: April 12, 2023
New mutation in the β1 propeller domain of LRP4 responsible for congenital myasthenic syndrome associated with Cenani-Lenz syndrome.
Journal: Scientific reports
Published: April 03, 2023
Last Updated: 09/26/2026