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C Angelini

Showing results (231-240 of 531) with videos related to

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Muscle & Nerve|May 1, 1985
Tubular aggregates: sarcoplasmic reticulum origin, calcium storage ability, and functional implicationsG Salviati, S Pierobon-Bormioli, R Betto, et al.
Biochemical and Biophysical Research Communications|May 25, 1995
MtDNA mutations associated with Leber's hereditary optic neuropathy: studies on cytoplasmic hybrid (cybrid) cellsL Vergani, A Martinuzzi, V Carelli, et al.
Clinical Genetics|March 27, 2009
Facioscapulohumeral muscular dystrophy: epidemiological and molecular study in a north-east Italian population sampleM L Mostacciuolo, E Pastorello, G Vazza, et al.
European Journal of Neurology|May 29, 2009
Epidemiology of ALS in Padova district, Italy, from 1992 to 2005V Cima, G Logroscino, C D'Ascenzo, et al.
Neuromuscular Disorders : NMD|July 1, 1994
Prevalent cardiac involvement in dystrophin Becker type mutationG Siciliano, M Fanin, C Angelini, et al.
Clinical Genetics|April 11, 2012
An intronic mutation causes severe LGMD2A in a large inbred family belonging to a genetic isolate in the AlpsM Fanin, F Benedicenti, C Fritegotto, et al.
Human Molecular Genetics|May 20, 1999
Myotonic dystrophy: tissue-specific effect of somatic CTG expansions on allele-specific DMAHP/SIX5 expressionZ Korade-Mirnics, J Tarleton, S Servidei, et al.
Italian Journal of Neurological Sciences|August 10, 2000
Positive correlation of CTG expansion and pharyngoesophageal alterations in myotonic dystrophy patientsM Marcon, C Briani, M Ermani, et al.
Journal of the American College of Cardiology|November 15, 1989
Type 1 fiber abnormalities in skeletal muscle of patients with hypertrophic and dilated cardiomyopathy: evidence of subclinical myogenic myopathyA L Caforio, B Rossi, R Risaliti, et al.
Digestive Diseases and Sciences|October 1, 1996
Esophageal motor function in patients with myotonic dystrophyM Costantini, G Zaninotto, M Anselmino, et al.
Pageof 54

Showing results (231-240 of 531) with videos related to

Sort By:
Pageof 54
Muscle & Nerve|May 1, 1985
Tubular aggregates: sarcoplasmic reticulum origin, calcium storage ability, and functional implicationsG Salviati, S Pierobon-Bormioli, R Betto, et al.
Biochemical and Biophysical Research Communications|May 25, 1995
MtDNA mutations associated with Leber's hereditary optic neuropathy: studies on cytoplasmic hybrid (cybrid) cellsL Vergani, A Martinuzzi, V Carelli, et al.
Clinical Genetics|March 27, 2009
Facioscapulohumeral muscular dystrophy: epidemiological and molecular study in a north-east Italian population sampleM L Mostacciuolo, E Pastorello, G Vazza, et al.
European Journal of Neurology|May 29, 2009
Epidemiology of ALS in Padova district, Italy, from 1992 to 2005V Cima, G Logroscino, C D'Ascenzo, et al.
Neuromuscular Disorders : NMD|July 1, 1994
Prevalent cardiac involvement in dystrophin Becker type mutationG Siciliano, M Fanin, C Angelini, et al.
Clinical Genetics|April 11, 2012
An intronic mutation causes severe LGMD2A in a large inbred family belonging to a genetic isolate in the AlpsM Fanin, F Benedicenti, C Fritegotto, et al.
Human Molecular Genetics|May 20, 1999
Myotonic dystrophy: tissue-specific effect of somatic CTG expansions on allele-specific DMAHP/SIX5 expressionZ Korade-Mirnics, J Tarleton, S Servidei, et al.
Italian Journal of Neurological Sciences|August 10, 2000
Positive correlation of CTG expansion and pharyngoesophageal alterations in myotonic dystrophy patientsM Marcon, C Briani, M Ermani, et al.
Journal of the American College of Cardiology|November 15, 1989
Type 1 fiber abnormalities in skeletal muscle of patients with hypertrophic and dilated cardiomyopathy: evidence of subclinical myogenic myopathyA L Caforio, B Rossi, R Risaliti, et al.
Digestive Diseases and Sciences|October 1, 1996
Esophageal motor function in patients with myotonic dystrophyM Costantini, G Zaninotto, M Anselmino, et al.
Pageof 54