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Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology
|
September 24, 2009
Mitochondrial disorders of the nuclear genome
C Angelini, L Bello, M Spinazzi, et al.
Biochimica Et Biophysica Acta
|
November 12, 1991
L-carnitine uptake in differentiating human cultured muscle
A Martinuzzi, L Vergani, M Rosa, et al.
Journal of Clinical Psychopharmacology
|
June 11, 2009
Increase in plasma levels of clozapine after addition of isoniazid
Michael C Angelini, Jacqueline MacCormack-Gagnon, Stephen Dizio
Annals of the New York Academy of Sciences
|
May 22, 2009
Distribution pattern of tyrosine hydroxylase in the brain and pituitary of the lungfish Protopterus annectens
F Bruzzone, M d'Amora, C Angelini, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology
|
May 31, 2001
Correlation of clinical function and muscle CT scan images in limb-girdle muscular dystrophy
M Vlak, E van der Kooi, C Angelini
Neurology
|
July 1, 1985
Carnitine deficiency, organic acidemias, and Reye's syndrome
D A Stumpf, W D Parker, C Angelini
Experimental Neurology
|
November 1, 1982
Carnitine, carnitine acyltransferases, and rat brain function
N Bresolin, L Freddo, L Vergani, et al.
European Neurology
|
January 1, 1995
Divergence of central nervous system involvement in 2 Italian sisters with congenital muscular dystrophy: a clinical and neuroradiological follow-up
C P Trevisan, F Martinello, E Ferruzza, et al.
Journal of Molecular and Cellular Cardiology
|
July 29, 1999
Could utrophin rescue the myocardium of patients with dystrophin gene mutations?
M Fanin, P Melacini, C Angelini, et al.
Rivista Di Neurologia
|
July 1, 1987
Quantitative histopathology in congenital myopathies
G Micaglio, M B Ceccato, C Trevisan, et al.
Page
of 54
Search research articles
Search
Showing results (61-70 of 531) with videos related to
Sort By:
Page
of 54
Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology
|
September 24, 2009
Mitochondrial disorders of the nuclear genome
C Angelini, L Bello, M Spinazzi, et al.
Biochimica Et Biophysica Acta
|
November 12, 1991
L-carnitine uptake in differentiating human cultured muscle
A Martinuzzi, L Vergani, M Rosa, et al.
Journal of Clinical Psychopharmacology
|
June 11, 2009
Increase in plasma levels of clozapine after addition of isoniazid
Michael C Angelini, Jacqueline MacCormack-Gagnon, Stephen Dizio
Annals of the New York Academy of Sciences
|
May 22, 2009
Distribution pattern of tyrosine hydroxylase in the brain and pituitary of the lungfish Protopterus annectens
F Bruzzone, M d'Amora, C Angelini, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology
|
May 31, 2001
Correlation of clinical function and muscle CT scan images in limb-girdle muscular dystrophy
M Vlak, E van der Kooi, C Angelini
Neurology
|
July 1, 1985
Carnitine deficiency, organic acidemias, and Reye's syndrome
D A Stumpf, W D Parker, C Angelini
Experimental Neurology
|
November 1, 1982
Carnitine, carnitine acyltransferases, and rat brain function
N Bresolin, L Freddo, L Vergani, et al.
European Neurology
|
January 1, 1995
Divergence of central nervous system involvement in 2 Italian sisters with congenital muscular dystrophy: a clinical and neuroradiological follow-up
C P Trevisan, F Martinello, E Ferruzza, et al.
Journal of Molecular and Cellular Cardiology
|
July 29, 1999
Could utrophin rescue the myocardium of patients with dystrophin gene mutations?
M Fanin, P Melacini, C Angelini, et al.
Rivista Di Neurologia
|
July 1, 1987
Quantitative histopathology in congenital myopathies
G Micaglio, M B Ceccato, C Trevisan, et al.
Page
of 54