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Y Campos

Showing results (41-50 of 121) with videos related to

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Muscle & Nerve|February 1, 1993
Plasma carnitine insufficiency and effectiveness of L-carnitine therapy in patients with mitochondrial myopathyY Campos, R Huertas, G Lorenzo, et al.
Revista De Neurologia|November 12, 1998
[Enzyme complex defects of the mitochondrial respiratory chain]J C Rubio, M A Martín, P del Hoyo, et al.
Annals of Neurology|March 20, 1998
Complex I defect in muscle from patients with Huntington's diseaseJ Arenas, Y Campos, R Ribacoba, et al.
Revista De Neurologia|November 12, 1998
[Molecular genetics of alterations in the mitochondrial respiratory chain]M A Martín, Y Campos, F de Bustos, et al.
Controlled Clinical Trials|June 1, 1996
Differences in basal nocturnal, meal-stimulated, and pentagastrin-stimulated gastric secretion values in a sample of healthy volunteers in basal conditions and under ranitidine influenceJ Carranza-Madrigal, J E Herrera-Abaraca, F Chavez-Carbajal, et al.
Journal of Internal Medicine|February 27, 2003
Intestinal pseudo-obstruction and urinary retention: cardinal features of a mitochondrial DNA-related diseaseA García-Velasco, C Gómez-Escalonilla, J M Guerra-Vales, et al.
Neuroscience Letters|December 18, 2016
Regional differences in mu-opioid receptor-dependent modulation of basal dopamine transmission in rat striatumY Campos-Jurado, L Martí-Prats, T Zornoza, et al.
Neurologia (Barcelona, Spain)|May 1, 1991
[Complex I (NADH coenzyme-Q-reductase) deficiency, MELAS syndrome and hypertrophic cardiomyopathy]C Márquez, J Bautista, J Arenas, et al.
Neurologia (Barcelona, Spain)|December 29, 1999
[Mitochondrial encephalomyopathy of late presentation with progressive ophthalmoplegia, tremor and diffuse leukoencephalopathy]E Franco, J Bautista, R Luque, et al.
Neuromuscular Disorders : NMD|June 26, 1999
McArdle's disease associated with homozygosity for the missense mutation Gly204Ser of the myophosphorylase gene in a Spanish patientJ C Rubio, M A Martín, A García, et al.
Pageof 13

Showing results (41-50 of 121) with videos related to

Sort By:
Pageof 13
Muscle & Nerve|February 1, 1993
Plasma carnitine insufficiency and effectiveness of L-carnitine therapy in patients with mitochondrial myopathyY Campos, R Huertas, G Lorenzo, et al.
Revista De Neurologia|November 12, 1998
[Enzyme complex defects of the mitochondrial respiratory chain]J C Rubio, M A Martín, P del Hoyo, et al.
Annals of Neurology|March 20, 1998
Complex I defect in muscle from patients with Huntington's diseaseJ Arenas, Y Campos, R Ribacoba, et al.
Revista De Neurologia|November 12, 1998
[Molecular genetics of alterations in the mitochondrial respiratory chain]M A Martín, Y Campos, F de Bustos, et al.
Controlled Clinical Trials|June 1, 1996
Differences in basal nocturnal, meal-stimulated, and pentagastrin-stimulated gastric secretion values in a sample of healthy volunteers in basal conditions and under ranitidine influenceJ Carranza-Madrigal, J E Herrera-Abaraca, F Chavez-Carbajal, et al.
Journal of Internal Medicine|February 27, 2003
Intestinal pseudo-obstruction and urinary retention: cardinal features of a mitochondrial DNA-related diseaseA García-Velasco, C Gómez-Escalonilla, J M Guerra-Vales, et al.
Neuroscience Letters|December 18, 2016
Regional differences in mu-opioid receptor-dependent modulation of basal dopamine transmission in rat striatumY Campos-Jurado, L Martí-Prats, T Zornoza, et al.
Neurologia (Barcelona, Spain)|May 1, 1991
[Complex I (NADH coenzyme-Q-reductase) deficiency, MELAS syndrome and hypertrophic cardiomyopathy]C Márquez, J Bautista, J Arenas, et al.
Neurologia (Barcelona, Spain)|December 29, 1999
[Mitochondrial encephalomyopathy of late presentation with progressive ophthalmoplegia, tremor and diffuse leukoencephalopathy]E Franco, J Bautista, R Luque, et al.
Neuromuscular Disorders : NMD|June 26, 1999
McArdle's disease associated with homozygosity for the missense mutation Gly204Ser of the myophosphorylase gene in a Spanish patientJ C Rubio, M A Martín, A García, et al.
Pageof 13