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Y Campos

Showing results (71-80 of 121) with videos related to

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Muscle & Nerve|July 1, 1993
Muscle carnitine deficiency and lipid storage myopathy in patients with mitochondrial myopathyY Campos, R Huertas, J Bautista, et al.
Neurologia (Barcelona, Spain)|August 1, 1994
[Complex I and IV deficits in the mitochondrial respiratory chain in two siblings with type I glutaric aciduria]A Martínez Bermejo, I Pascual Castroviejo, B Merinero, et al.
Human Mutation|September 15, 2004
Four novel mutations in patients from the Middle East with the infantile form of GM1-gangliosidosisT Georgiou, A Drousiotou, Y Campos, et al.
Neuromuscular Disorders : NMD|March 17, 2007
A novel mutation in the mitochondrial DNA tRNA Leu (UUR) gene associated with late-onset ocular myopathyE Maeso, A Rueda, S Jiménez, et al.
Journal of Biochemical and Biophysical Methods|October 12, 2002
Comparison of different ligand densities for the manufacture of CB Hep-1 immunosorbentsL Gómez, R Hernández, N Ibarra, et al.
Muscle & Nerve|March 15, 2000
Lipomatosis, proximal myopathy, and the mitochondrial 8344 mutation. A lipid storage myopathy?A Muñoz-Málaga, J Bautista, J A Salazar, et al.
Acta Neurologica Scandinavica|October 1, 1994
Benign mitochondrial myopathy with decreased succinate cytochrome C reductase activityJ Arpa, Y Campos, M Gutiérrez-Molina, et al.
Biochimica Et Biophysica Acta|November 9, 2000
Myocardial carnitine and carnitine palmitoyltransferase deficiencies in patients with severe heart failureM A Martín, M A Gómez, F Guillén, et al.
Stroke|November 3, 2001
Mitochondrial disease and strokeE Martínez-Fernández, A Gil-Peralta, R García-Lozano, et al.
Neurologia (Barcelona, Spain)|October 1, 1994
[Clinical and investigative approaches in mitochondrial diseases. A review of 15 cases]J Arpa, Y Campos, A Cruz Martínez, et al.
Pageof 13

Showing results (71-80 of 121) with videos related to

Sort By:
Pageof 13
Muscle & Nerve|July 1, 1993
Muscle carnitine deficiency and lipid storage myopathy in patients with mitochondrial myopathyY Campos, R Huertas, J Bautista, et al.
Neurologia (Barcelona, Spain)|August 1, 1994
[Complex I and IV deficits in the mitochondrial respiratory chain in two siblings with type I glutaric aciduria]A Martínez Bermejo, I Pascual Castroviejo, B Merinero, et al.
Human Mutation|September 15, 2004
Four novel mutations in patients from the Middle East with the infantile form of GM1-gangliosidosisT Georgiou, A Drousiotou, Y Campos, et al.
Neuromuscular Disorders : NMD|March 17, 2007
A novel mutation in the mitochondrial DNA tRNA Leu (UUR) gene associated with late-onset ocular myopathyE Maeso, A Rueda, S Jiménez, et al.
Journal of Biochemical and Biophysical Methods|October 12, 2002
Comparison of different ligand densities for the manufacture of CB Hep-1 immunosorbentsL Gómez, R Hernández, N Ibarra, et al.
Muscle & Nerve|March 15, 2000
Lipomatosis, proximal myopathy, and the mitochondrial 8344 mutation. A lipid storage myopathy?A Muñoz-Málaga, J Bautista, J A Salazar, et al.
Acta Neurologica Scandinavica|October 1, 1994
Benign mitochondrial myopathy with decreased succinate cytochrome C reductase activityJ Arpa, Y Campos, M Gutiérrez-Molina, et al.
Biochimica Et Biophysica Acta|November 9, 2000
Myocardial carnitine and carnitine palmitoyltransferase deficiencies in patients with severe heart failureM A Martín, M A Gómez, F Guillén, et al.
Stroke|November 3, 2001
Mitochondrial disease and strokeE Martínez-Fernández, A Gil-Peralta, R García-Lozano, et al.
Neurologia (Barcelona, Spain)|October 1, 1994
[Clinical and investigative approaches in mitochondrial diseases. A review of 15 cases]J Arpa, Y Campos, A Cruz Martínez, et al.
Pageof 13