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C Angelini

Showing results (71-80 of 531) with videos related to

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Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology|April 20, 2004
Morphological changes in late onset acid Maltase deficient patients with splicing gene mutationC Angelini, G Cenacchi, A C Nascimbeni, et al.
Neuromuscular Disorders : NMD|July 17, 1999
Prenatal diagnosis in a family affected with beta-sarcoglycan muscular dystrophyE Pegoraro, M Fanin, C Angelini, et al.
Annals of Neurology|December 1, 1978
Carnitine deficiency: acute postpartum crisisC Angelini, E Govoni, M M Bragaglia, et al.
Human Mutation|June 30, 2000
Private beta- and gamma-sarcoglycan gene mutations: evidence of a founder effect in Northern ItalyM Fanin, E P Hoffman, C Angelini, et al.
Cell Biology and Toxicology|January 29, 2008
The sea urchin, Paracentrotus lividus, embryo as a "bioethical" model for neurodevelopmental toxicity testing: effects of diazinon on the intracellular distribution of OTX2-like proteinsM G Aluigi, C Angelini, G Corte, et al.
Human Genetics|February 11, 1977
Duchenne muscular dystrophy. A population studyG A Danieli, M L Mostacciuolo, A Bonfante, et al.
Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology|November 24, 2011
Dysferlinopathy course and sportive activity: clues for possible treatmentC Angelini, E Peterle, A Gaiani, et al.
Muscle & Nerve|January 1, 1989
Myosin heavy chain composition of muscle fibers in spinal muscular atrophyD Biral, E Scarpini, C Angelini, et al.
Archives of Neurology|September 1, 1973
Mitochondria-lipid-glycogen (MLG) disease of muscle. A morphologically regressive congenital myopathyF Jerusalem, C Angelini, A G Engel, et al.
Experimental Neurology|January 1, 1982
Autoimmune neuromuscular disease induced by a preparation of choline acetyltransferaseL P Chao, K S Kan, C Angelini, et al.
Pageof 54

Showing results (71-80 of 531) with videos related to

Sort By:
Pageof 54
Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology|April 20, 2004
Morphological changes in late onset acid Maltase deficient patients with splicing gene mutationC Angelini, G Cenacchi, A C Nascimbeni, et al.
Neuromuscular Disorders : NMD|July 17, 1999
Prenatal diagnosis in a family affected with beta-sarcoglycan muscular dystrophyE Pegoraro, M Fanin, C Angelini, et al.
Annals of Neurology|December 1, 1978
Carnitine deficiency: acute postpartum crisisC Angelini, E Govoni, M M Bragaglia, et al.
Human Mutation|June 30, 2000
Private beta- and gamma-sarcoglycan gene mutations: evidence of a founder effect in Northern ItalyM Fanin, E P Hoffman, C Angelini, et al.
Cell Biology and Toxicology|January 29, 2008
The sea urchin, Paracentrotus lividus, embryo as a "bioethical" model for neurodevelopmental toxicity testing: effects of diazinon on the intracellular distribution of OTX2-like proteinsM G Aluigi, C Angelini, G Corte, et al.
Human Genetics|February 11, 1977
Duchenne muscular dystrophy. A population studyG A Danieli, M L Mostacciuolo, A Bonfante, et al.
Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology|November 24, 2011
Dysferlinopathy course and sportive activity: clues for possible treatmentC Angelini, E Peterle, A Gaiani, et al.
Muscle & Nerve|January 1, 1989
Myosin heavy chain composition of muscle fibers in spinal muscular atrophyD Biral, E Scarpini, C Angelini, et al.
Archives of Neurology|September 1, 1973
Mitochondria-lipid-glycogen (MLG) disease of muscle. A morphologically regressive congenital myopathyF Jerusalem, C Angelini, A G Engel, et al.
Experimental Neurology|January 1, 1982
Autoimmune neuromuscular disease induced by a preparation of choline acetyltransferaseL P Chao, K S Kan, C Angelini, et al.
Pageof 54