Bruno Eymard

发表

Lamin A/C gene related disorders: the EUROMEN consortium experience

Luciano Merlini, Francesco Muntoni, M. de Visser, 2003 .

A nomenclature and classification for the congenital myasthenic syndromes: preparing for FAIR data in the genomic era

Rachel Thompson, Hanns Lochmüller, Bruno Eymard, 2018, Orphanet Journal of Rare Diseases.

Deciphering the complexity of the 4q and 10q subtelomeres by molecular combing in healthy individuals and patients with facioscapulohumeral dystrophy

Albert David, Jon Andoni Urtizberea, Bruno Eymard, 2019, Journal of Medical Genetics.

Atrial flutter in myotonic dystrophy type 1: Patient characteristics and clinical outcome

Guillaume Bassez, Bruno Eymard, Arnaud Lazarus, 2016, Neuromuscular Disorders.

Relationship between muscle impairments, postural stability, and gait parameters assessed with lower-trunk accelerometry in myotonic dystrophy type 1

Luc J. Hébert, Guillaume Bassez, Bruno Eymard, 2016, Neuromuscular Disorders.

Quadriceps strength is a sensitive marker of disease progression in sporadic inclusion body myositis

Bruno Eymard, Jean-Yves Hogrel, Aurélie Canal, 2012, Neuromuscular Disorders.

Prevalence and correlates of apathy in myotonic dystrophy type 1

Bruno Eymard, Cynthia Gagnon, B. Eymard, 2015, BMC Neurology.

Long-term observational study of sporadic inclusion body myositis.

David Hilton-Jones, Bruno Eymard, Waney Squier, 2011, Brain : a journal of neurology.

Diagnostic and clinical classification of autoimmune myasthenia gravis.

Bruno Eymard, B. Eymard, S. Berrih-Aknin, 2014, Journal of autoimmunity.

Shared blood and muscle CD8+ T-cell expansions in inclusion body myositis.

Olivier Boyer, Bruno Eymard, David Klatzmann, 2006, Brain : a journal of neurology.

Genetic Characterization of a French Cohort of GNE‐mutation negative inclusion body myopathy patients with exome sequencing

Svetlana Gorokhova, Jean-François Deleuze, Bruno Eymard, 2017, Muscle & nerve.