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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 AngeliniActa Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology|April 20, 2004
Morphological changes in late onset acid Maltase deficient patients with splicing gene mutationC Angelini, G Cenacchi, A C Nascimbeni, et al.International Review of Cell and Molecular Biology|January 11, 2017
Molecular Mechanisms of Noncanonical AutophagyN Dupont, A C Nascimbeni, E Morel, et al.Cell 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.Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|July 4, 2006
Epilepsy and limb girdle muscular dystrophy type 2A: double trouble, serendipitous finding or new phenotype?C Pizzanelli, M Mancuso, R Galli, et al.Human Mutation|June 29, 2004
Molecular diagnosis in LGMD2A: mutation analysis or protein testing?M Fanin, L Fulizio, A C Nascimbeni, et al.Pageof 2