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American Journal of Human Genetics|May 1, 1983
Incidence of Friedreich ataxia in Italy estimated from consanguineous marriagesG Romeo, P Menozzi, A Ferlini, et al.Italian Journal of Neurological Sciences|August 1, 1987
Needle biopsy for muscle diagnosis and research: an Italian experienceF Dworzak, L Morandi, S Daniel, et al.The Journal of Clinical Investigation|August 1, 1995
Expression of transforming growth factor-beta 1 in dystrophic patient muscles correlates with fibrosis. Pathogenetic role of a fibrogenic cytokineP Bernasconi, E Torchiana, P Confalonieri, et al.Journal of Neuroimmunology|September 1, 1984
Studies on terminal deoxynucleotidyl transferase and adenosine deaminase in myasthenic thymusP Vezzoni, F Fiacchino, L Clerici, et al.Journal of Neurology|March 1, 1992
Efficacy of intranasal administration of neostigmine in myasthenic patientsA Sghirlanzoni, D Pareyson, C Benvenuti, et al.Neurology|July 1, 1991
Dominantly inherited mitochondrial myopathy with multiple deletions of mitochondrial DNA: clinical, morphologic, and biochemical studiesS Servidei, M Zeviani, G Manfredi, et al.Journal of Neurology|July 10, 1999
Clinical and molecular studies of 73 Italian families with autosomal dominant cerebellar ataxia type I: SCA1 and SCA2 are the most common genotypesD Pareyson, C Gellera, B Castellotti, et al.International Surgery|January 1, 1996
Detection and morphology of thymic remnants after video-assisted thoracoscopic extended thymectomy (VATET) in patients with myasthenia gravisR Scelsi, M T Ferrò, L Scelsi, et al.Neuromuscular Disorders : NMD|May 1, 1994
Lysosomal glycogen storage with normal acid maltase: a familial study with successful heart transplantF Dworzak, F Casazza, M Mora, et al.Journal of Neurology|January 1, 1993
Evidence of a genetic marker associated with early onset in Friedreich's ataxiaS Cocozza, A Antonelli, G Campanella, et al.Pageof 16