121st ENMC International Workshop on Desmin and Protein Aggregate Myopathies. 7–9 November 2003, Naarden, The Netherlands

This publication has 34 references indexed in Scilit:

• Desmin‐related myopathy with mallory body–like inclusions is caused by mutations of the selenoprotein N gene
  Annals of Neurology, 2004
• Desmin myopathy
  Brain, 2004
• Myofibrillar myopathy caused by novel dominant negative αB‐crystallin mutations
  Annals of Neurology, 2003
• Desmin – Protein Surplus Myopathies, 96th European Neuromuscular Centre (ENMC)-sponsored International Workshop held 14–16 September 2001, Naarden, The Netherlands
  Neuromuscular Disorders, 2002
• A missense mutation in the αB-crystallin chaperone gene causes a desmin-related myopathy
  Nature Genetics, 1998
• Missense mutations in desmin associated with familial cardiac and skeletal myopathy
  Nature Genetics, 1998
• Familial desmin-related myopathies and cardiomyopathies — from myopathology to molecular and clinical genetics
  Neuromuscular Disorders, 1996
• Desmin in myology 24th European Neuromuscular Center-sponsored workshop held 5–6 November 1993, Naarden, The Netherlands
  Neuromuscular Disorders, 1995
• A form of congenital muscular dystrophy
  Brain & Development, 1980
• Autosomal dominant “spheroid body myopathy”
  Muscle & Nerve, 1978