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C Angelini

Showing results (211-220 of 531) with videos related to

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Muscle & Nerve|September 1, 1997
Changes in skeletal muscle histology and metabolism in patients undergoing exercise deconditioning: effect of propionyl-L-carnitineG Brevetti, M Fanin, V De Amicis, et al.
Biological Psychiatry|August 6, 1999
Cognitive impairment and (CTG)n expansion in myotonic dystrophy patientsG I Perini, E Menegazzo, M Ermani, et al.
The Journal of Clinical Investigation|October 1, 1993
Expression of muscle-type phosphorylase in innervated and aneural cultured muscle of patients with myophosphorylase deficiencyA Martinuzzi, L Vergani, R Carrozzo, et al.
American Journal of Medical Genetics|February 2, 1996
X-inactivation patterns in female Leber's hereditary optic neuropathy patients do not support a strong X-linked determinantE Pegoraro, V Carelli, M Zeviani, et al.
Neuromuscular Disorders : NMD|August 1, 1996
Discordant clinical outcome in type III spinal muscular atrophy sibships showing the same deletion patternF Capon, C Levato, L Merlini, et al.
Journal of Wildlife Diseases|August 12, 2008
Detection of chytridiomycosis caused by Batrachochytrium dendrobatidis in the endangered Sardinian newt (Euproctus platycephalus) in southern Sardinia, ItalyS Bovero, G Sotgiu, C Angelini, et al.
Human Genetics|July 1, 1994
A study on duplications of the dystrophin gene: evidence of a geographical difference in the distribution of breakpoints by intronF Galvagni, F A Saad, G A Danieli, et al.
The New England Journal of Medicine|December 11, 1980
Systemic carnitine deficiency--a treatable inherited lipid-storage disease presenting as Reye's syndromeP R Chapoy, C Angelini, W J Brown, et al.
Journal of Neurogenetics|January 1, 1987
Myotonic dystrophy and chromosome translocation segregating in the same familyG Neri, E Bertini, A Serra, et al.
European Journal of Histochemistry : EJH|December 14, 2004
Acetylcholine synthesis and possible functions during sea urchin developmentC Angelini, B Baccetti, P Piomboni, et al.
Pageof 54

Showing results (211-220 of 531) with videos related to

Sort By:
Pageof 54
Muscle & Nerve|September 1, 1997
Changes in skeletal muscle histology and metabolism in patients undergoing exercise deconditioning: effect of propionyl-L-carnitineG Brevetti, M Fanin, V De Amicis, et al.
Biological Psychiatry|August 6, 1999
Cognitive impairment and (CTG)n expansion in myotonic dystrophy patientsG I Perini, E Menegazzo, M Ermani, et al.
The Journal of Clinical Investigation|October 1, 1993
Expression of muscle-type phosphorylase in innervated and aneural cultured muscle of patients with myophosphorylase deficiencyA Martinuzzi, L Vergani, R Carrozzo, et al.
American Journal of Medical Genetics|February 2, 1996
X-inactivation patterns in female Leber's hereditary optic neuropathy patients do not support a strong X-linked determinantE Pegoraro, V Carelli, M Zeviani, et al.
Neuromuscular Disorders : NMD|August 1, 1996
Discordant clinical outcome in type III spinal muscular atrophy sibships showing the same deletion patternF Capon, C Levato, L Merlini, et al.
Journal of Wildlife Diseases|August 12, 2008
Detection of chytridiomycosis caused by Batrachochytrium dendrobatidis in the endangered Sardinian newt (Euproctus platycephalus) in southern Sardinia, ItalyS Bovero, G Sotgiu, C Angelini, et al.
Human Genetics|July 1, 1994
A study on duplications of the dystrophin gene: evidence of a geographical difference in the distribution of breakpoints by intronF Galvagni, F A Saad, G A Danieli, et al.
The New England Journal of Medicine|December 11, 1980
Systemic carnitine deficiency--a treatable inherited lipid-storage disease presenting as Reye's syndromeP R Chapoy, C Angelini, W J Brown, et al.
Journal of Neurogenetics|January 1, 1987
Myotonic dystrophy and chromosome translocation segregating in the same familyG Neri, E Bertini, A Serra, et al.
European Journal of Histochemistry : EJH|December 14, 2004
Acetylcholine synthesis and possible functions during sea urchin developmentC Angelini, B Baccetti, P Piomboni, et al.
Pageof 54