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Neuromuscular Disorders : NMD|December 7, 2002
The phenotypic manifestations of autosomal recessive axonal Charcot-Marie-Tooth due to a mutation in Lamin A/C geneM Chaouch, Y Allal, A De Sandre-Giovannoli, et al.
Neuromuscular Disorders : NMD|December 7, 2002
Hepatitis C virus infection and myositis: a virus localization studyA Di Muzio, B Bonetti, M Capasso, et al.
Neuromuscular Disorders : NMD|December 7, 2002
The spectrum of pathology in central core diseaseC A Sewry, C Müller, M Davis, et al.
Neuromuscular Disorders : NMD|December 7, 2002
Skeletal muscle of mice with a mutation in slow alpha-tropomyosin is weaker at lower lengthsA de Haan, M R van der Vliet, I M P Gommans, et al.
Neuromuscular Disorders : NMD|October 26, 2002
Inclusion body myositis: morphological clues to correct diagnosisK Dahlbom, C Lindberg, A Oldfors
Neuromuscular Disorders : NMD|October 26, 2002
Early onset of cardiomyopathy in two brothers with X-linked Emery-Dreifuss muscular dystrophyUlvi Astra Talkop, Inga Talvik, Margit Sõnajalg, et al.
Neuromuscular Disorders : NMD|October 26, 2002
Stiff-person syndrome associated with oral isotretinoin treatmentE Chroni, Th Sakkis, S Georgiou, et al.
Neuromuscular Disorders : NMD|May 29, 2002
Severe progressive form of congenital muscular dystrophy with calf pseudohypertrophy, macroglossia and respiratory insufficiencySusana Quijano-Roy, Lucía Galan, Ana Ferreiro, et al.
Neuromuscular Disorders : NMD|May 29, 2002
Novel deletion at the M and P promoters of the human dystrophin gene associated with a Duchenne muscular dystrophyGiulia Frisso, Simone Sampaolo, Lucio Pastore, et al.
Neuromuscular Disorders : NMD|May 29, 2002
Rapid scanning of myotubularin (MTM1) gene by denaturing high-performance liquid chromatography (DHPLC)Elisabetta Flex, Alessandro De Luca, Maria Rosaria D'Apice, et al.
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