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Muscle & Nerve|August 1, 1991
Glucocorticoids and immunosuppressants do not change the prevalence of necrosis and regeneration in mdx skeletal musclesB Weller, R Massa, G Karpati, et al.Muscle & Nerve|July 1, 1979
Cylindrical spirals in human skeletal muscleS Carpenter, G Karpati, Y Robitaille, et al.Neuromuscular Disorders : NMD|July 10, 1999
Myopathy with trabecular muscle fibersB Weller, S Carpenter, H Lochmüller, et al.Neurology|October 1, 1976
The childhood type of dermatomyositisS Carpenter, G Karpati, S Rothman, et al.Neurology|January 1, 1978
Inclusion body myositis: a distinct variety of idiopathic inflammatory myopathyS Carpenter, G Karpati, I Heller, et al.Neurology|January 1, 1977
Juvenile dystonic lipidosis: an unusual form of neurovisceral storage diseaseG Karpati, S Carpenter, L S Wolfe, et al.Brain : a Journal of Neurology|June 1, 1980
A distinct form of adult polyglucosan body disease with massive involvement of central and peripheral neuronal processes and astrocytes: a report of four cases and a review of the occurrence of polyglucosan bodies in other conditions such as Lafora's disease and normal ageingY Robitaille, S Carpenter, G Karpati, et al.Annals of Neurology|July 1, 1986
Myopathy caused by a deficiency of Ca2+-adenosine triphosphatase in sarcoplasmic reticulum (Brody's disease)G Karpati, J Charuk, S Carpenter, et al.Archives of Neurology|May 1, 1991
Familial inclusion body myositis among Kurdish-Iranian JewsR Massa, B Weller, G Karpati, et al.Pageof 90