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Muscle & Nerve
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May 1, 1985
Tubular aggregates: sarcoplasmic reticulum origin, calcium storage ability, and functional implications
G 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) cells
L 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 sample
M 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 2005
V Cima, G Logroscino, C D'Ascenzo, et al.
Neuromuscular Disorders : NMD
|
July 1, 1994
Prevalent cardiac involvement in dystrophin Becker type mutation
G 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 Alps
M 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 expression
Z 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 patients
M 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 myopathy
A L Caforio, B Rossi, R Risaliti, et al.
Digestive Diseases and Sciences
|
October 1, 1996
Esophageal motor function in patients with myotonic dystrophy
M Costantini, G Zaninotto, M Anselmino, et al.
Page
of 54
Search research articles
Search
Showing results (231-240 of 531) with videos related to
Sort By:
Page
of 54
Muscle & Nerve
|
May 1, 1985
Tubular aggregates: sarcoplasmic reticulum origin, calcium storage ability, and functional implications
G 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) cells
L 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 sample
M 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 2005
V Cima, G Logroscino, C D'Ascenzo, et al.
Neuromuscular Disorders : NMD
|
July 1, 1994
Prevalent cardiac involvement in dystrophin Becker type mutation
G 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 Alps
M 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 expression
Z 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 patients
M 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 myopathy
A L Caforio, B Rossi, R Risaliti, et al.
Digestive Diseases and Sciences
|
October 1, 1996
Esophageal motor function in patients with myotonic dystrophy
M Costantini, G Zaninotto, M Anselmino, et al.
Page
of 54