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Biochemical and Biophysical Research Communications|August 12, 1999
Increased number of caveolae and caveolin-3 overexpression in Duchenne muscular dystrophyS Repetto, M Bado, P Broda, et al.Neurology|April 4, 2000
Mutation in the CAV3 gene causes partial caveolin-3 deficiency and hyperCKemiaI Carbone, C Bruno, F Sotgia, et al.Neurology|June 1, 1994
Abnormalities in the expression of beta-spectrin in Duchenne muscular dystrophyC Minetti, K Tanji, P G Rippa, et al.Neuropediatrics|November 1, 1982
Familial nemaline myopathyG Scarlato, G Pellegrini, M Moggio, et al.Minerva Pediatrica|October 1, 1991
[Infantile dermatomyositis. Clinical aspects and prospective treatments]G Cordone, A Buoncompagni, O Ciccone, et al.European Journal of Pediatrics|October 1, 1993
Dystrophinopathy in two young boys with exercise-induced cramps and myoglobinuriaC Minetti, K Tanji, H W Chang, et al.Nature Genetics|April 16, 1998
Mutations in the caveolin-3 gene cause autosomal dominant limb-girdle muscular dystrophyC Minetti, F Sotgia, C Bruno, et al.Neuromuscular Disorders : NMD|November 2, 1999
A novel missense mutation in the glycogen branching enzyme gene in a child with myopathy and hepatopathyC Bruno, M DiRocco, L D Lamba, et al.Applied Optics|November 19, 2010
Reduction in correlation-filter sensitivity to background clutter by the automatic spatial frequency selection algorithmC Minetti, F DuboisCurrent Opinion in Genetics & Development|June 23, 1999
Muscular dystrophies: alterations in a limited number of cellular pathways?D Toniolo, C MinettiPageof 11