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C Angelini

Showing results (251-260 of 531) with videos related to

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Journal of the American College of Cardiology|January 1, 1995
Correlation between cardiac involvement and CTG trinucleotide repeat length in myotonic dystrophyP Melacini, C Villanova, E Menegazzo, et al.
Cell Death and Differentiation|May 1, 2010
Normal myogenesis and increased apoptosis in myotonic dystrophy type-1 muscle cellsE Loro, F Rinaldi, A Malena, et al.
Revue Neurologique|January 1, 2017
Cerebral venous thrombosis at high altitude: A systematic reviewC Zavanone, M Panebianco, M Yger, et al.
Circulation|April 1, 1988
Increases in walking distance in patients with peripheral vascular disease treated with L-carnitine: a double-blind, cross-over studyG Brevetti, M Chiariello, G Ferulano, et al.
Brain : a Journal of Neurology|December 3, 1999
Riboflavin therapy. Biochemical heterogeneity in two adult lipid storage myopathiesL Vergani, M Barile, C Angelini, et al.
Neuroepidemiology|January 1, 1993
Reappraisal of the incidence rate of Duchenne and Becker muscular dystrophies on the basis of molecular diagnosisM L Mostacciuolo, M Miorin, E Pegoraro, et al.
La Radiologia Medica|October 1, 1995
[Imaging of the thymus gland in myasthenia gravis (computerized tomography and magnetic resonance)]A Tregnaghi, A De Candia, M Calderone, et al.
Giornale Italiano Di Cardiologia|January 1, 1980
[The heart in myotonic dystrophy. Clinical and instrumental study in 17 patients (author's transl)]M Ferrari, M Armani, P Melacini, et al.
Journal of Neuropathology and Experimental Neurology|March 14, 2001
Caspase 3 expression correlates with skeletal muscle apoptosis in Duchenne and facioscapulo human muscular dystrophy. A potential target for pharmacological treatment?M Sandri, A H El Meslemani, C Sandri, et al.
European Neurology|January 1, 1990
Serum lipids, lipoprotein analysis and apoprotein A-I, A-II and B levels in Friedreich's ataxiaG Baldo-Enzi, M Bernardo, E Vitale, et al.
Pageof 54

Showing results (251-260 of 531) with videos related to

Sort By:
Pageof 54
Journal of the American College of Cardiology|January 1, 1995
Correlation between cardiac involvement and CTG trinucleotide repeat length in myotonic dystrophyP Melacini, C Villanova, E Menegazzo, et al.
Cell Death and Differentiation|May 1, 2010
Normal myogenesis and increased apoptosis in myotonic dystrophy type-1 muscle cellsE Loro, F Rinaldi, A Malena, et al.
Revue Neurologique|January 1, 2017
Cerebral venous thrombosis at high altitude: A systematic reviewC Zavanone, M Panebianco, M Yger, et al.
Circulation|April 1, 1988
Increases in walking distance in patients with peripheral vascular disease treated with L-carnitine: a double-blind, cross-over studyG Brevetti, M Chiariello, G Ferulano, et al.
Brain : a Journal of Neurology|December 3, 1999
Riboflavin therapy. Biochemical heterogeneity in two adult lipid storage myopathiesL Vergani, M Barile, C Angelini, et al.
Neuroepidemiology|January 1, 1993
Reappraisal of the incidence rate of Duchenne and Becker muscular dystrophies on the basis of molecular diagnosisM L Mostacciuolo, M Miorin, E Pegoraro, et al.
La Radiologia Medica|October 1, 1995
[Imaging of the thymus gland in myasthenia gravis (computerized tomography and magnetic resonance)]A Tregnaghi, A De Candia, M Calderone, et al.
Giornale Italiano Di Cardiologia|January 1, 1980
[The heart in myotonic dystrophy. Clinical and instrumental study in 17 patients (author's transl)]M Ferrari, M Armani, P Melacini, et al.
Journal of Neuropathology and Experimental Neurology|March 14, 2001
Caspase 3 expression correlates with skeletal muscle apoptosis in Duchenne and facioscapulo human muscular dystrophy. A potential target for pharmacological treatment?M Sandri, A H El Meslemani, C Sandri, et al.
European Neurology|January 1, 1990
Serum lipids, lipoprotein analysis and apoprotein A-I, A-II and B levels in Friedreich's ataxiaG Baldo-Enzi, M Bernardo, E Vitale, et al.
Pageof 54