Bruno Eymard

Overview

Best Publications

• Clinical and molecular genetic spectrum of autosomal dominant Emery‐Dreifuss muscular dystrophy due to mutations of the lamin A/C gene

  Bonne G;Mercuri E;Muchir A;Urtizberea A

  570
  Citations

• Mutations in dynamin 2 cause dominant centronuclear myopathy.

  Marc Bitoun;Svetlana Maugenre;Pierre-Yves Jeannet;Emmanuelle Lacène

  485
  Citations

• Electromyography guides toward subgroups of mutations in muscle channelopathies

  Emmanuel Fournier;Marianne Arzel;Damien Sternberg;Savine Vicart

  378
  Citations

• Perindopril preventive treatment on mortality in Duchenne muscular dystrophy: 10 years' follow-up

  Denis Duboc;Christophe Meune;Bertrand Pierre;Karim Wahbi

  377
  Citations

• Diagnostic and clinical classification of autoimmune myasthenia gravis

  Sonia Berrih-Aknin;Mélinée Frenkian-Cuvelier;Bruno Eymard

  328
  Citations

• Long-term observational study of sporadic inclusion body myositis

  Olivier Benveniste;Marguerite Guiguet;Jane Freebody;Odile Dubourg

  320
  Citations

• Anti-HMGCR autoantibodies in European patients with autoimmune necrotizing myopathies: inconstant exposure to statin.

  Yves Allenbach;Laurent Drouot;Aude Rigolet;Jean Luc Charuel

  312
  Citations

• Results and long-term followup of intravenous immunoglobulin infusions in chronic, refractory polymyositis: an open study with thirty-five adult patients.

  Patrick Cherin;S Pelletier;A Teixeira;P Laforet

  305
  Citations

• New nomenclature and DNA testing guidelines for myotonic dystrophy type 1 (DM1)

  T. Ashizawa;I. Gonzales;N. Ohsawa;R. H. Singer

  295
  Citations

• Phenotypic Study in 40 Patients With Dysferlin Gene Mutations: High Frequency of Atypical Phenotypes

  Karine Nguyen;Guillaume Bassez;Martin Krahn;Rafaelle Bernard

  280
  Citations

• High risk of cancer in autoimmune necrotizing myopathies: usefulness of myositis specific antibody.

  Yves Allenbach;Jeremy Keraen;Anne-Marie Bouvier;Valérie Jooste

  279
  Citations

• High incidence of sudden death with conduction system and myocardial disease due to lamins A and C gene mutation.

  Henri‐Marc Bécane;Gisèle Bonne;Shaida Varnous;Antoine Muchir

  277
  Citations

• Juvenile and adult-onset acid maltase deficiency in France: genotype-phenotype correlation.

  P. Laforêt;M. Nicolino;B. Eymard;J.P. Puech

  272
  Citations

• Mutations of the FHL1 Gene Cause Emery-Dreifuss Muscular Dystrophy

  Lucie Gueneau;Lucie Gueneau;Anne T. Bertrand;Anne T. Bertrand;Jean-Philippe Jais;Mustafa A. Salih

  253
  Citations

• Primary adhalinopathy: a common cause of autosomal recessive muscular dystrophy of variable severity

  F. Piccolo;S.L. Roberds;M. Jeanpierre;F. Leturcq

  248
  Citations

• Correlation of anti–signal recognition particle autoantibody levels with creatine kinase activity in patients with necrotizing myopathy

  Olivier Benveniste;Laurent Drouot;Fabienne Jouen;Jean-Luc Charuel

  241
  Citations

• Calpainopathy—A Survey of Mutations and Polymorphisms

  I. Richard;C. Roudaut;A. Saenz;R. Pogue

  233
  Citations

• Distinct muscle imaging patterns in myofibrillar myopathies

  D. Fischer;R. A. Kley;K. Strach;C. Meyer

  227
  Citations

• An IRF8-binding promoter variant and AIRE control CHRNA1 promiscuous expression in thymus

  Matthieu Giraud;Richard Taubert;Claire Vandiedonck;Xiayi Ke

  222
  Citations

• Mutation in the Human Acetylcholinesterase-Associated Collagen Gene, COLQ, Is Responsible for Congenital Myasthenic Syndrome with End-Plate Acetylcholinesterase Deficiency (Type Ic)

  Claire Donger;Eric Krejci;Adolf Pou Serradell;Bruno Eymard

  215
  Citations