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C Angelini

Showing results (201-210 of 531) with videos related to

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Annals of Neurology|October 1, 1991
Is the carboxyl-terminus of dystrophin required for membrane association? A novel, severe case of Duchenne muscular dystrophyE P Hoffman, C A Garcia, J S Chamberlain, et al.
Circulation|October 1, 1991
Muscle carnitine deficiency in patients with severe peripheral vascular diseaseG Brevetti, C Angelini, M Rosa, et al.
Molecular and Cellular Biochemistry|October 8, 1990
Liver fatty acid-binding protein in two cases of human lipid storageL Vergani, M Fanin, A Martinuzzi, et al.
American Journal of Medical Genetics|March 1, 1994
Occurrence of two different intragenic deletions in two male relatives affected with Duchenne muscular dystrophyM L Mostacciuolo, M Miorin, L Vitiello, et al.
Biochemical and Biophysical Research Communications|August 4, 1995
Survival motor neuron gene transcript analysis in muscles from spinal muscular atrophy patientsM Gennarelli, M Lucarelli, F Capon, et al.
The Journal of Experimental Biology|July 7, 2001
Synthesis of the signal molecule acetylcholine during the developmental cycle of Paramecium primaurelia (Protista, Ciliophora) and its possible function in conjugationM U Delmonte Corrado, H Politi, M Ognibene, et al.
Acta Neurologica|April 1, 1981
Atrio-ventricular conduction system in myotonic dystrophy: value of electrophysiological investigationP Melacini, C Egloff, M Armani, et al.
Revue Neurologique|January 1, 1991
Multicenter trial with ubidecarenone: treatment of 44 patients with mitochondrial myopathiesG Scarlato, N Bresolin, I Moroni, et al.
Muscle & Nerve|May 1, 1985
Familial neuromuscular disease with tubular aggregatesS Pierobon-Bormioli, M Armani, S P Ringel, et al.
Acta Psychiatrica Scandinavica|April 1, 1988
Psychiatric disturbances associated with myasthenia gravisG Magni, G F Micaglio, R Lalli, et al.
Pageof 54

Showing results (201-210 of 531) with videos related to

Sort By:
Pageof 54
Annals of Neurology|October 1, 1991
Is the carboxyl-terminus of dystrophin required for membrane association? A novel, severe case of Duchenne muscular dystrophyE P Hoffman, C A Garcia, J S Chamberlain, et al.
Circulation|October 1, 1991
Muscle carnitine deficiency in patients with severe peripheral vascular diseaseG Brevetti, C Angelini, M Rosa, et al.
Molecular and Cellular Biochemistry|October 8, 1990
Liver fatty acid-binding protein in two cases of human lipid storageL Vergani, M Fanin, A Martinuzzi, et al.
American Journal of Medical Genetics|March 1, 1994
Occurrence of two different intragenic deletions in two male relatives affected with Duchenne muscular dystrophyM L Mostacciuolo, M Miorin, L Vitiello, et al.
Biochemical and Biophysical Research Communications|August 4, 1995
Survival motor neuron gene transcript analysis in muscles from spinal muscular atrophy patientsM Gennarelli, M Lucarelli, F Capon, et al.
The Journal of Experimental Biology|July 7, 2001
Synthesis of the signal molecule acetylcholine during the developmental cycle of Paramecium primaurelia (Protista, Ciliophora) and its possible function in conjugationM U Delmonte Corrado, H Politi, M Ognibene, et al.
Acta Neurologica|April 1, 1981
Atrio-ventricular conduction system in myotonic dystrophy: value of electrophysiological investigationP Melacini, C Egloff, M Armani, et al.
Revue Neurologique|January 1, 1991
Multicenter trial with ubidecarenone: treatment of 44 patients with mitochondrial myopathiesG Scarlato, N Bresolin, I Moroni, et al.
Muscle & Nerve|May 1, 1985
Familial neuromuscular disease with tubular aggregatesS Pierobon-Bormioli, M Armani, S P Ringel, et al.
Acta Psychiatrica Scandinavica|April 1, 1988
Psychiatric disturbances associated with myasthenia gravisG Magni, G F Micaglio, R Lalli, et al.
Pageof 54