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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 mutation
C Angelini, G Cenacchi, A C Nascimbeni, et al.
Neuromuscular Disorders : NMD
|
July 17, 1999
Prenatal diagnosis in a family affected with beta-sarcoglycan muscular dystrophy
E Pegoraro, M Fanin, C Angelini, et al.
Annals of Neurology
|
December 1, 1978
Carnitine deficiency: acute postpartum crisis
C 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 Italy
M 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 proteins
M G Aluigi, C Angelini, G Corte, et al.
Human Genetics
|
February 11, 1977
Duchenne muscular dystrophy. A population study
G 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 treatment
C Angelini, E Peterle, A Gaiani, et al.
Muscle & Nerve
|
January 1, 1989
Myosin heavy chain composition of muscle fibers in spinal muscular atrophy
D Biral, E Scarpini, C Angelini, et al.
Archives of Neurology
|
September 1, 1973
Mitochondria-lipid-glycogen (MLG) disease of muscle. A morphologically regressive congenital myopathy
F Jerusalem, C Angelini, A G Engel, et al.
Experimental Neurology
|
January 1, 1982
Autoimmune neuromuscular disease induced by a preparation of choline acetyltransferase
L P Chao, K S Kan, C Angelini, et al.
Page
of 54
Search research articles
Search
Showing results (71-80 of 531) with videos related to
Sort By:
Page
of 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 mutation
C Angelini, G Cenacchi, A C Nascimbeni, et al.
Neuromuscular Disorders : NMD
|
July 17, 1999
Prenatal diagnosis in a family affected with beta-sarcoglycan muscular dystrophy
E Pegoraro, M Fanin, C Angelini, et al.
Annals of Neurology
|
December 1, 1978
Carnitine deficiency: acute postpartum crisis
C 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 Italy
M 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 proteins
M G Aluigi, C Angelini, G Corte, et al.
Human Genetics
|
February 11, 1977
Duchenne muscular dystrophy. A population study
G 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 treatment
C Angelini, E Peterle, A Gaiani, et al.
Muscle & Nerve
|
January 1, 1989
Myosin heavy chain composition of muscle fibers in spinal muscular atrophy
D Biral, E Scarpini, C Angelini, et al.
Archives of Neurology
|
September 1, 1973
Mitochondria-lipid-glycogen (MLG) disease of muscle. A morphologically regressive congenital myopathy
F Jerusalem, C Angelini, A G Engel, et al.
Experimental Neurology
|
January 1, 1982
Autoimmune neuromuscular disease induced by a preparation of choline acetyltransferase
L P Chao, K S Kan, C Angelini, et al.
Page
of 54