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Neuromuscular Disorders : NMD
|
January 1, 1992
Prevalence of dystrophin-positive fibers in 85 Duchenne muscular dystrophy patients
M Fanin, G A Danieli, L Vitiello, et al.
Neurology
|
March 1, 1984
Myoglobinuria and carnitine palmityltransferase (CPT) deficiency: studies with malonyl-CoA suggest absence of only CPT-II
C P Trevisan, C Angelini, L Freddo, et al.
Human Genetics
|
January 1, 1980
Duchenne muscular dystrophy: data from family studies
G A Danieli, M L Mostacciuolo, G Pilotto, et al.
Rivista Di Neurologia
|
May 1, 1982
[Preliminary study on the use of acetylcarnitine in patients with mental deterioration]
G Testa, D Giaretta, A Pellegrini, et al.
Pediatric Research
|
December 1, 1980
Plasma and urine carnitine levels during development
P A Battistella, L Vergani, F Donzelli, et al.
European Neurology
|
January 1, 1986
Malonyl-CoA abnormal inhibition of residual enzyme activity in carnitine palmitoyltransferase deficiency
C P Trevisan, C Angelini, L A Fiorellini, et al.
Annals of Neurology
|
January 1, 1980
Multisystem triglyceride storage disorder with impaired long-chain fatty acid oxidation
C Angelini, M Philippart, C Borrone, et al.
Neuromuscular Disorders : NMD
|
January 1, 1996
Skeletal muscle sarcoplasmic reticulum phenotype in myotonic dystrophy
E Damiani, C Angelini, M Pelosi, et al.
Neurology
|
March 14, 2001
Calpain-3 and dysferlin protein screening in patients with limb-girdle dystrophy and myopathy
M Fanin, E Pegoraro, C Matsuda-Asada, et al.
Journal of Managed Care & Specialty Pharmacy
|
April 26, 2014
Implementation of an opioid management initiative by a state Medicaid program
Maria M Garcia, Michael C Angelini, Tara Thomas, et al.
Page
of 54
Search research articles
Search
Showing results (101-110 of 531) with videos related to
Sort By:
Page
of 54
Neuromuscular Disorders : NMD
|
January 1, 1992
Prevalence of dystrophin-positive fibers in 85 Duchenne muscular dystrophy patients
M Fanin, G A Danieli, L Vitiello, et al.
Neurology
|
March 1, 1984
Myoglobinuria and carnitine palmityltransferase (CPT) deficiency: studies with malonyl-CoA suggest absence of only CPT-II
C P Trevisan, C Angelini, L Freddo, et al.
Human Genetics
|
January 1, 1980
Duchenne muscular dystrophy: data from family studies
G A Danieli, M L Mostacciuolo, G Pilotto, et al.
Rivista Di Neurologia
|
May 1, 1982
[Preliminary study on the use of acetylcarnitine in patients with mental deterioration]
G Testa, D Giaretta, A Pellegrini, et al.
Pediatric Research
|
December 1, 1980
Plasma and urine carnitine levels during development
P A Battistella, L Vergani, F Donzelli, et al.
European Neurology
|
January 1, 1986
Malonyl-CoA abnormal inhibition of residual enzyme activity in carnitine palmitoyltransferase deficiency
C P Trevisan, C Angelini, L A Fiorellini, et al.
Annals of Neurology
|
January 1, 1980
Multisystem triglyceride storage disorder with impaired long-chain fatty acid oxidation
C Angelini, M Philippart, C Borrone, et al.
Neuromuscular Disorders : NMD
|
January 1, 1996
Skeletal muscle sarcoplasmic reticulum phenotype in myotonic dystrophy
E Damiani, C Angelini, M Pelosi, et al.
Neurology
|
March 14, 2001
Calpain-3 and dysferlin protein screening in patients with limb-girdle dystrophy and myopathy
M Fanin, E Pegoraro, C Matsuda-Asada, et al.
Journal of Managed Care & Specialty Pharmacy
|
April 26, 2014
Implementation of an opioid management initiative by a state Medicaid program
Maria M Garcia, Michael C Angelini, Tara Thomas, et al.
Page
of 54