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Neuromuscular Disorders : NMD|May 1, 1994
Immunohistochemical analysis of perforin and granzyme A in inflammatory myopathiesS Orimo, R Koga, K Goto, et al.Neuromuscular Disorders : NMD|January 1, 1995
Recurrent congenital arthrogryposis leading to a diagnosis of myasthenia gravis in an initially asymptomatic motherP R Barnes, D J Kanabar, L Brueton, et al.Neuromuscular Disorders : NMD|January 1, 1995
Absence of mutations in the Mn superoxide dismutase or catalase genes in familial amyotrophic lateral sclerosisJ S Parboosingh, G A Rouleau, V Meninger, et al.Neuromuscular Disorders : NMD|March 14, 2008
Familial aggregation of white matter lesions in myotonic dystrophy type 1Alfonso Di Costanzo, Lucio Santoro, Mario de Cristofaro, et al.Neuromuscular Disorders : NMD|March 1, 1995
Differential diagnosis of periodic paralysis aided by in vitro myographyP A Iaizzo, S Quasthoff, F Lehmann-HornNeuromuscular Disorders : NMD|March 1, 1994
Expression of the 43 kDa dystrophin-associated glycoprotein in human neuromuscular diseaseT R Helliwell, T M Nguyen, G E MorrisNeuromuscular Disorders : NMD|March 1, 1994
Deficiency of the 50 kDa dystrophin-associated glycoprotein and abnormal expression of utrophin in two south Asian cousins with variable expression of severe childhood autosomal recessive muscular dystrophyC A Sewry, A Sansome, K Matsumura, et al.Neuromuscular Disorders : NMD|March 1, 1994
A Danish family with limb-girdle muscular dystrophy with autosomal dominant inheritanceJ F Nielsen, J JakobsenNeuromuscular Disorders : NMD|July 1, 1994
Cognitive impairment in Duchenne muscular dystrophyN Bresolin, E Castelli, G P Comi, et al.Neuromuscular Disorders : NMD|September 1, 1993
Prader-Willi syndrome: diagnostic strategy with a cytogenetic and molecular approachP Malzac, A Moncla, M A Voelckel, et al.Pageof 340