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Human Molecular Genetics|July 1, 1995
Mapping of genes predisposing to idiopathic generalized epilepsyF Zara, A Bianchi, G Avanzini, et al.Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|July 12, 2002
Is the CACNA1A gene involved in familial migraine with aura?R Brugnoni, M Leone, A Rigamonti, et al.Neuromuscular Disorders : NMD|July 1, 1995
Lack of mRNA and dystrophin expression in DMD patients three months after myoblast transferL Morandi, P Bernasconi, M Gebbia, et al.Helvetica Paediatrica Acta|March 1, 1984
Myoadenylate deaminase deficiency in a 5-year-old boy with intermittent muscle painL N Rossi, F Cornelio, F Dworzak, et al.Italian Journal of Neurological Sciences|April 1, 1988
Anti AChR antibody: relevance to diagnosis and clinical aspects of myasthenia gravisR Mantegazza, D Pareyson, F Baggi, et al.Journal of Neuroimmunology|August 1, 1996
Major histocompatibility complex class II molecule expression on muscle cells is regulated by differentiation: implications for the immunopathogenesis of muscle autoimmune diseasesR Mantegazza, M Gebbia, M Mora, et al.Acta Neuropathologica. Supplementum|January 1, 1981
Systemic carnitine deficiency with peripheral nerve involvement morphological and biochemical studyF Cornelio, D Peluchetti, M Rimoldi, et al.Neuroreport|January 6, 1999
Retroviral-mediated transfer of the galactocerebrosidase gene in neural progenitor cellsE Torchiana, L Lulli, E Cattaneo, et al.Italian Journal of Neurological Sciences|October 1, 1988
Growth hormone evaluation in Duchenne muscular dystrophyL Merlini, C Granata, A Ballestrazzi, et al.American Journal of Human Genetics|April 16, 1998
Ataxia with isolated vitamin E deficiency: heterogeneity of mutations and phenotypic variability in a large number of familiesL Cavalier, K Ouahchi, H J Kayden, et al.Pageof 16