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Neuromuscular Disorders

Articles from the last few issues of Neuromuscular Disorders © Elsevier
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  • Commentary from the Editor
    Neuromuscular Disorders, Vol. 14, No. 1. (January 2004), pp. 1-3.
    by V Dubowitz
  • Identification of a locus for an autosomal recessive hyaline body myopathy at chromosome 3p22.2-p21.32
    Neuromuscular Disorders, Vol. 14, No. 1. (January 2004), pp. 4-9.
    by S Onengut, SA Ugur, H Karasoy, N Yuceyar, A Tolun
  • Dystrophinopathy caused by mid-intronic substitutions activating cryptic exons in the DMD gene
    Neuromuscular Disorders, Vol. 14, No. 1. (January 2004), pp. 10-18.
    by C Beroud, A Carrie, C Beldjord, N Deburgrave, S Llense, N Carelle, C Peccate, JM Cuisset, F Pandit, F Carre-Pigeon, M Mayer, R Bellance, D Recan, J Chelly, JC Kaplan, F Leturcq
  • A-utrophin up-regulation in mdx skeletal muscle is independent of regeneration
    Neuromuscular Disorders, Vol. 14, No. 1. (January 2004), pp. 19-23.
    by AP Weir, JE Morgan, KE Davies
  • Electrophysiological and morphological characterization of a case of autosomal recessive congenital myasthenic syndrome with acetylcholine receptor deficiency due to a N88K rapsyn homozygous mutation
    Neuromuscular Disorders, Vol. 14, No. 1. (January 2004), pp. 24-32.
    by E Yasaki, C Prioleau, J Barbier, P Richard, F Andreux, JP Leroy, P Dartevelle, J Koenig, J Molgo, M Fardeau, B Eymard, D Hantai
  • Asymptomatic carriers and gender differences in facioscapulohumeral muscular dystrophy (FSHD)
    Neuromuscular Disorders, Vol. 14, No. 1. (January 2004), pp. 33-38.
    by MMO Tonini, MR Passos-Bueno, A Cerqueira, SR Matioli, R Pavanello, M Zatz
  • Changes in motor cortex excitability in facioscapulohumeral muscular dystrophy
    Neuromuscular Disorders, Vol. 14, No. 1. (January 2004), pp. 39-45.
    by V Di Lazzaro, A Oliviero, PA Tonali, L Felicetti, MBP De Marco, E Saturno, F Pilato, M Pescatori, M Dileone, P Pasqualetti, E Ricci
  • A novel mutation in the mitochondrial tRNAPhe gene associated with mitochondrial myopathy
    Neuromuscular Disorders, Vol. 14, No. 1. (January 2004), pp. 46-50.
    by AR Moslemi, C Lindberg, J Toft, E Holme, G Kollberg, A Oldfors
  • Muscle MRI in adult-onset acid maltase deficiency
    Neuromuscular Disorders, Vol. 14, No. 1. (January 2004), pp. 51-55.
    by A Pichiecchio, C Uggetti, S Ravaglia, MG Egitto, M Rossi, G Sandrini, C Danesino
  • 117th ENMC Workshop: Ventilatory Support in Congenital Neuromuscular Disorders - Congenital Myopathies, Congenital Muscular Dystrophies, Congenital Myotonic Dystrophy and SMA (II) 4-6 April 2003, Naarden, The Netherlands
    Neuromuscular Disorders, Vol. 14, No. 1. (January 2004), pp. 56-69.
    by C Wallgren-Pettersson, K Bushby, U Mellies, A Simonds
  • 2003 International Friedreich's Ataxia Research Conference, 14-16 February 2003, Bethesda, MD, USA
    Neuromuscular Disorders, Vol. 14, No. 1. (January 2004), pp. 70-82.
    by H Seznec, RB Wilson, H Puccio
  • Clinical Neurology - Manson Publishing, 2002, ISBN 1-84076-010-9, 768 pages, 85.00
    Neuromuscular Disorders, Vol. 14, No. 1. (January 2004), pp. 83-83.
    by GJ Hankey, JM Wardlaw
  • Electrodiagnosis in Diseases of Nerve and Muscle: Principles and Practice, 3rd edition - Jun Kimura (Ed.); Oxford University Press, 2001, 9911 pages, hardback, ISBN 0-l9-512977-6, 105
    Neuromuscular Disorders, Vol. 14, No. 1. (January 2004), pp. 83-83.
    by JW Day
  • Muscular Dystrophy - the Facts - Alan E.H. Emery; 2nd ed.; Oxford University Press, 2000, 157 pages, paperback, ISBN 0-19-263217-5, 12.99
    Neuromuscular Disorders, Vol. 14, No. 1. (January 2004), pp. 84-84.
    by S Gazzard
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