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Arthritis and Rheumatism
|
November 1, 1996
Abnormal carnitine distribution in the muscles of patients with idiopathic inflammatory myopathy
J Arenas, M R Gonzalez-Crespo, Y Campos, et al.
Molecular Genetics and Metabolism
|
March 22, 2003
New mutations in two Dutch patients with early infantile galactosialidosis
J Groener, P Maaswinkel-Mooy, V Smit, et al.
Biochemical and Biophysical Research Communications
|
September 23, 1997
Bilateral striatal necrosis and MELAS associated with a new T3308C mutation in the mitochondrial ND1 gene
Y Campos, M A Martín, J C Rubio, et al.
Revista De Neurologia
|
September 21, 2000
[Mitochondrial encephalopathies]
M Castro-Gago, M I Novo-Rodríguez, E Pintos-Martínez, et al.
The American Journal of Clinical Nutrition
|
March 13, 1998
Effects of L-carnitine on erythrocyte acyl-CoA, free CoA, and glycerophospholipid acyltransferase in uremia
B de los Reyes, J A Navarro, R Pérez-García, et al.
Neuromuscular Disorders : NMD
|
March 11, 2000
Single large-scale mitochondrial DNA deletion in a patient with encephalopathy, cardiomyopathy, and prominent intestinal pseudo-obstruction
Y Campos, M A Martín, C Caballero, et al.
Journal of Child Neurology
|
March 1, 1996
Leber's congenital amaurosis associated with mitochondrial dysfunction
M Castro-Gago, E Pintos-Martínez, A Beiras-Iglesias, et al.
Clinical Chemistry
|
April 1, 1993
Respiratory chain enzyme activities in lymphocytes from untreated patients with Parkinson disease
N Barroso, Y Campos, R Huertas, et al.
Biochemical and Biophysical Research Communications
|
October 15, 1992
Respiratory chain enzymes in muscle of endurance athletes: effect of L-carnitine
R Huertas, Y Campos, E Díaz, et al.
Neurologia (Barcelona, Spain)
|
October 1, 1995
[Adult onset mitochondrial myopathy without ophthalmoplegia. Four cases attributable to complex III and IV deficits in the respiratory chain]
J Bautista, A Muñoz-Málaga, I Chinchón, et al.
Page
of 13
Search research articles
Search
Showing results (51-60 of 121) with videos related to
Sort By:
Page
of 13
Arthritis and Rheumatism
|
November 1, 1996
Abnormal carnitine distribution in the muscles of patients with idiopathic inflammatory myopathy
J Arenas, M R Gonzalez-Crespo, Y Campos, et al.
Molecular Genetics and Metabolism
|
March 22, 2003
New mutations in two Dutch patients with early infantile galactosialidosis
J Groener, P Maaswinkel-Mooy, V Smit, et al.
Biochemical and Biophysical Research Communications
|
September 23, 1997
Bilateral striatal necrosis and MELAS associated with a new T3308C mutation in the mitochondrial ND1 gene
Y Campos, M A Martín, J C Rubio, et al.
Revista De Neurologia
|
September 21, 2000
[Mitochondrial encephalopathies]
M Castro-Gago, M I Novo-Rodríguez, E Pintos-Martínez, et al.
The American Journal of Clinical Nutrition
|
March 13, 1998
Effects of L-carnitine on erythrocyte acyl-CoA, free CoA, and glycerophospholipid acyltransferase in uremia
B de los Reyes, J A Navarro, R Pérez-García, et al.
Neuromuscular Disorders : NMD
|
March 11, 2000
Single large-scale mitochondrial DNA deletion in a patient with encephalopathy, cardiomyopathy, and prominent intestinal pseudo-obstruction
Y Campos, M A Martín, C Caballero, et al.
Journal of Child Neurology
|
March 1, 1996
Leber's congenital amaurosis associated with mitochondrial dysfunction
M Castro-Gago, E Pintos-Martínez, A Beiras-Iglesias, et al.
Clinical Chemistry
|
April 1, 1993
Respiratory chain enzyme activities in lymphocytes from untreated patients with Parkinson disease
N Barroso, Y Campos, R Huertas, et al.
Biochemical and Biophysical Research Communications
|
October 15, 1992
Respiratory chain enzymes in muscle of endurance athletes: effect of L-carnitine
R Huertas, Y Campos, E Díaz, et al.
Neurologia (Barcelona, Spain)
|
October 1, 1995
[Adult onset mitochondrial myopathy without ophthalmoplegia. Four cases attributable to complex III and IV deficits in the respiratory chain]
J Bautista, A Muñoz-Málaga, I Chinchón, et al.
Page
of 13