Showing results (1-10 of 76) with videos related to
Sort By:
Pageof 8
Journal of the Neurological Sciences|May 1, 1994
Absence of dystrophin and spectrin in regenerating muscle fibers from Becker dystrophy patientsM Fanin, E Pegoraro, C AngeliniHuman Mutation|June 30, 2000
Private beta- and gamma-sarcoglycan gene mutations: evidence of a founder effect in Northern ItalyM Fanin, E P Hoffman, C Angelini, et al.Neuromuscular Disorders : NMD|July 17, 1999
Prenatal diagnosis in a family affected with beta-sarcoglycan muscular dystrophyE Pegoraro, M Fanin, C Angelini, et al.Neuropathology and Applied Neurobiology|February 4, 2009
Muscle histopathology in myasthenia gravis with antibodies against MuSK and AChRS Martignago, M Fanin, E Albertini, et al.Neuromuscular Disorders : NMD|July 19, 2003
LGMD2E patients risk developing dilated cardiomyopathyM Fanin, P Melacini, C Boito, et al.Neurology|March 14, 2001
Calpain-3 and dysferlin protein screening in patients with limb-girdle dystrophy and myopathyM Fanin, E Pegoraro, C Matsuda-Asada, et al.AJNR. American Journal of Neuroradiology|March 27, 1999
MR imaging findings in children with merosin-deficient congenital muscular dystrophyP A Caro, M Scavina, E Hoffman, et al.Neurology|November 9, 2000
A novel laminin alpha2 isoform in severe laminin alpha2 deficient congenital muscular dystrophyE Pegoraro, M Fanin, C P Trevisan, et al.European Journal of Neurology|October 24, 2018
Insights into the genetic epidemiology of spinal and bulbar muscular atrophy: prevalence estimation and multiple founder haplotypes in the Veneto Italian regionC Bertolin, G Querin, I Martinelli, et al.Journal of the Neurological Sciences|September 1, 1996
alpha-Sarcoglycan (adhalin) deficiency: complete deficiency patients are 5% of childhood-onset dystrophin-normal muscular dystrophy and most partial deficiency patients do not have gene mutationsD J Duggan, M Fanin, E Pegoraro, et al.Pageof 8