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Neurology|April 4, 2000
Mutation in the CAV3 gene causes partial caveolin-3 deficiency and hyperCKemiaI Carbone, C Bruno, F Sotgia, et al.Neurology|August 26, 1998
Unusual EEG pattern linked to chromosome 3p in a family with idiopathic generalized epilepsyF Zara, M Labuda, P G Garofalo, et al.Neuropediatrics|July 4, 2007
Revelation of a novel CLN5 mutation in early juvenile neuronal ceroid lipofuscinosisN Cannelli, N Nardocci, D Cassandrini, et al.Handbook of Clinical Neurology|April 19, 2011
Caveolinopathies: translational implications of caveolin-3 in skeletal and cardiac muscle disordersE Gazzerro, A Bonetto, C MinettiEpilepsy Research|December 4, 2003
Absence of mutations in major GEFS+ genes in myoclonic astatic epilepsyR Nabbout, A Kozlovski, E Gennaro, et al.Neurology|September 1, 1992
Immunologic study of vinculin in Duchenne muscular dystrophyC Minetti, K Tanji, E BonillaNeurology|December 1, 1991
Progressive depletion of fast alpha-actinin-positive muscle fibers in Duchenne muscular dystrophyC Minetti, E Ricci, E BonillaEuropean Journal of Neurology|October 2, 2012
Early-onset absence epilepsy: SLC2A1 gene analysis and treatment evolutionS Agostinelli, M Traverso, P Accorsi, et al.FEBS Letters|July 1, 1999
Localization of the human caveolin-3 gene to the D3S18/D3S4163/D3S4539 locus (3p25), in close proximity to the human oxytocin receptor gene. Identification of the caveolin-3 gene as a candidate for deletion in 3p-syndromeF Sotgia, C Minetti, M P LisantiLaboratory Investigation; a Journal of Technical Methods and Pathology|August 26, 1998
Apoptotic myonuclei in human Duchenne muscular dystrophyM Sandri, C Minetti, M Pedemonte, et al.Pageof 97