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Neuropathology and Applied Neurobiology|February 19, 2013
Muscle atrophy in Limb Girdle Muscular Dystrophy 2A: a morphometric and molecular studyM Fanin, A C Nascimbeni, C AngeliniJournal of Medical Genetics|September 15, 2006
Screening of calpain-3 autolytic activity in LGMD muscle: a functional map of CAPN3 gene mutationsM Fanin, A C Nascimbeni, C AngeliniCell Death and Differentiation|May 19, 2012
The role of autophagy in the pathogenesis of glycogen storage disease type II (GSDII)A C Nascimbeni, M Fanin, E Masiero, et al.Journal of Medical Genetics|May 29, 2007
Correlations between clinical severity, genotype and muscle pathology in limb girdle muscular dystrophy type 2AM Fanin, L Nardetto, A C Nascimbeni, et al.Neurology|April 22, 2009
Frequency of LGMD gene mutations in Italian patients with distinct clinical phenotypesM Fanin, A C Nascimbeni, S Aurino, et al.Neurological Research|January 23, 2010
The clinical course of calpainopathy (LGMD2A) and dysferlinopathy (LGMD2B)C Angelini, L Nardetto, C Borsato, et al.Journal of the Neurological Sciences|August 18, 1999
Regeneration in sarcoglycanopathies: expression studies of sarcoglycans and other muscle proteinsM Fanin, C AngeliniNeuropathology and Applied Neurobiology|November 26, 2002
Muscle pathology in dysferlin deficiencyM Fanin, C AngeliniNeuropathology and Applied Neurobiology|June 13, 2002
Defective assembly of sarcoglycan complex in patients with beta-sarcoglycan gene mutations. Study of aneural and innervated cultured myotubesM Fanin, C AngeliniItalian Journal of Neurological Sciences|January 1, 1993
Multifactorial study of inflammatory myopathies. Report of 29 casesC Angelini, E Menegazzo, M FaninPageof 49