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Acta Neuropathologica|January 1, 1975
Congenital myopathy with "reducing bodies" in muscle fibresF M Tomé, M FardeauNeuromuscular Disorders : NMD|December 10, 1997
Oculopharyngeal muscular dystrophy in FranceM Fardeau, F M ToméCurrent Opinion in Neurology|December 16, 1998
Hereditary inclusion body myopathiesF M Tomé, M FardeauPathologia Europaea|January 1, 1976
Ultrastructural study of a muscle biopsy in a case of GM1 gangliosidosis type IF M Tomé, M FardeauActa Neuropathologica|January 1, 1980
Nuclear inclusions in oculopharyngeal dystrophyF M Tomé, M FardeauNeuromuscular Disorders : NMD|July 1, 1993
Ubiquitin and beta-amyloid-protein in inclusion body myositis (IBM), familial IBM-like disorder and oculopharyngeal muscular dystrophy: an immunocytochemical studyA Leclerc, F M Tomé, M FardeauArchives of Neurology|October 1, 1976
Familial fingerprint body myopathyM Fardeau, F M Tomé, S DerambureMuscle & Nerve|January 1, 1979
Muscle and nerve changes induced by perhexiline maleate in man and miceM Fardeau, F M Tomé, P SimonActa Neuropathologica|June 15, 1977
Ultrastructure of muscle and sensory nerve in Fabry's diseaseF M Tomé, M Fardeau, G LenoirPageof 26