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Neuromuscular Diseases Evaluations

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SECTION HEADS

  • Photo of Daniel Drachman

    Daniel Drachman

    Neuromuscular Laboratory, Department of Neurology, Johns Hopkins School of Medicine, Baltimore, MD, USA

  • Photo of Michael Hanna

    Michael Hanna

    UCL Institute of Neurology, University College London, London, UK

Section Topics

  • » Channelopathies
  • » Disorders of the neuromuscular junction: acquired autoimmune
  • » Disorders of the neuromuscular junction: acquired toxic
  • » Disorders of the neuromuscular junction: congenital myasthenic syndromes
  • » Electrodiagnostic testing
  • » Inflammatory myopathies
  • » Metabolic myopathies
  • » Motor neuropathies
  • » Muscular dystrophies
  • » Other inherited & congenital muscle disorders (e.g. Emery Dreifuss, oculopharyngeal, familial IBM)
  • » Therapy for neuromuscular diseases: gene therapy
  • » Therapy for neuromuscular diseases: immunomodulatory
  • » Therapy for neuromuscular diseases: other
  • » Toxic myopathies

LATEST EVALUATION

Published back to back with a paper by Sato and Sato {1}, the paper by Al Rawi et al. elegantly explains the mechanism by which paternal mitochondrial (mt)DNA is removed during the...

Massimo Zeviani and Carlo Viscomi, National Neurological Institute 'Carlo Besta', Italy. F1000 Neurological Disorders

8 Must Read

TOP RATED ARTICLE THIS WEEK [FREE TO VIEW]

10
Postfertilization autophagy of sperm organelles prevents paternal mitochondrial DNA transmission.

Al Rawi S, Louvet-Vallée S, Djeddi A, Sachse M, ..., Hajjar C, Boyd L, Legouis R, Galy V. Science. 2011 Nov 25; 334(6059):1144-7

2 Evaluations, most recent by

Dolores Lamb and Alexander W. Pastuszak, Baylor College of Medicine, USA. F1000 Urology

  • New Finding

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