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M Villanova

Showing results (51-60 of 85) with videos related to

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Brain Research|February 19, 1993
Rimmed vacuoles of inclusion body myositis and oculopharyngeal muscular dystrophy contain amyloid precursor protein and lysosomal markersM Villanova, M Kawai, U Lübke, et al.
Acta Neuropathologica|February 9, 2000
Hepatitis C virus infection and myositis: a polymerase chain reaction studyM Villanova, C Caudai, P Sabatelli, et al.
Neuromuscular Disorders : NMD|March 1, 1997
Intracellular detection of laminin alpha 2 chain in skin by electron microscopy immunocytochemistry: comparison between normal and laminin alpha 2 chain deficient subjectsS Squarzoni, M Villanova, P Sabatelli, et al.
Neuromuscular Disorders : NMD|July 19, 2000
A novel SURF1 mutation results in Leigh syndrome with peripheral neuropathy caused by cytochrome c oxidase deficiencyL Santoro, R Carrozzo, A Malandrini, et al.
Muscle & Nerve|July 9, 1999
Nuclear changes in a case of X-linked Emery-Dreifuss muscular dystrophyA Ognibene, P Sabatelli, S Petrini, et al.
European Neurology|September 28, 1998
CAG repeat expansion in an italian family with spinocerebellar ataxia type 2 (SCA2): a clinical and genetic studyA Malandrini, L Galli, M Villanova, et al.
Brain & Development|October 7, 1998
Neuronal intranuclear inclusion disease: neuropathologic study of a caseA Malandrini, M Villanova, S Tripodi, et al.
Biochemical and Biophysical Research Communications|November 4, 2000
Unusual laminin alpha2 processing in myoblasts from a patient with a novel variant of congenital muscular dystrophyG Lattanzi, F Muntoni, P Sabatelli, et al.
Clinical Genetics|June 6, 2003
Neurological presentation of Ehlers-Danlos syndrome type IV in a family with parental mosaicismS Palmeri, F Mari, I Meloni, et al.
Journal of the Neurological Sciences|April 30, 1998
Juvenile Leigh syndrome with protracted course presenting as chronic sensory motor neuropathy, ataxia, deafness and retinitis pigmentosa: a clinicopathological reportA Malandrini, S Palmeri, G M Fabrizi, et al.
Pageof 9

Showing results (51-60 of 85) with videos related to

Sort By:
Pageof 9
Brain Research|February 19, 1993
Rimmed vacuoles of inclusion body myositis and oculopharyngeal muscular dystrophy contain amyloid precursor protein and lysosomal markersM Villanova, M Kawai, U Lübke, et al.
Acta Neuropathologica|February 9, 2000
Hepatitis C virus infection and myositis: a polymerase chain reaction studyM Villanova, C Caudai, P Sabatelli, et al.
Neuromuscular Disorders : NMD|March 1, 1997
Intracellular detection of laminin alpha 2 chain in skin by electron microscopy immunocytochemistry: comparison between normal and laminin alpha 2 chain deficient subjectsS Squarzoni, M Villanova, P Sabatelli, et al.
Neuromuscular Disorders : NMD|July 19, 2000
A novel SURF1 mutation results in Leigh syndrome with peripheral neuropathy caused by cytochrome c oxidase deficiencyL Santoro, R Carrozzo, A Malandrini, et al.
Muscle & Nerve|July 9, 1999
Nuclear changes in a case of X-linked Emery-Dreifuss muscular dystrophyA Ognibene, P Sabatelli, S Petrini, et al.
European Neurology|September 28, 1998
CAG repeat expansion in an italian family with spinocerebellar ataxia type 2 (SCA2): a clinical and genetic studyA Malandrini, L Galli, M Villanova, et al.
Brain & Development|October 7, 1998
Neuronal intranuclear inclusion disease: neuropathologic study of a caseA Malandrini, M Villanova, S Tripodi, et al.
Biochemical and Biophysical Research Communications|November 4, 2000
Unusual laminin alpha2 processing in myoblasts from a patient with a novel variant of congenital muscular dystrophyG Lattanzi, F Muntoni, P Sabatelli, et al.
Clinical Genetics|June 6, 2003
Neurological presentation of Ehlers-Danlos syndrome type IV in a family with parental mosaicismS Palmeri, F Mari, I Meloni, et al.
Journal of the Neurological Sciences|April 30, 1998
Juvenile Leigh syndrome with protracted course presenting as chronic sensory motor neuropathy, ataxia, deafness and retinitis pigmentosa: a clinicopathological reportA Malandrini, S Palmeri, G M Fabrizi, et al.
Pageof 9