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Y Campos

Showing results (61-70 of 121) with videos related to

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Anales Espanoles De Pediatria|January 1, 1993
[Mitochondrial myopathy caused by complex III and IV deficiency. A familial case]M Castro-Gago, I Novo-Rodríguez, T García Caballero, et al.
Journal of the Neurological Sciences|January 8, 1999
Myophosphorylase deficiency associated with a defect in complex I of the mitochondrial respiratory chainJ C Rubio, M A Martín, J Bautista, et al.
Revista De Neurologia|July 2, 2008
[Association between autistic spectrum and mitochondrial pathology]M Castro-Gago, O Blanco-Barca, C Gómez-Lado, et al.
Neurology|August 1, 1997
Leigh syndrome associated with the T9176C mutation in the ATPase 6 gene of mitochondrial DNAY Campos, M A Martín, J C Rubio, et al.
Revista De Neurologia|September 20, 2001
[MELAS syndrome masquerading as herpes encephalitis: genetic diagnosis]M de Toledo, J Díaz-Guzmán, D A Pérez-Martínez, et al.
Journal of the Neurological Sciences|November 10, 2001
Mitochondrial DNA point mutation in the COI gene in a patient with McArdle's diseaseI Aguilera, J R García-Lozano, A Muñoz, et al.
Neuromuscular Disorders : NMD|September 21, 2000
A mitochondrial tRNA(Lys) gene mutation (T8316C) in a patient with mitochondrial myopathy, lactic acidosis, and stroke-like episodesY Campos, G Lorenzo, M A Martín, et al.
The Journal of Pediatrics|November 1, 1994
Encephalopathy, petechiae, and acrocyanosis with ethylmalonic aciduria associated with muscle cytochrome c oxidase deficiencyM T García-Silva, Y Campos, A Ribes, et al.
Neurology|May 1, 1996
Respiratory-chain enzyme activities in isolated mitochondria of lymphocytes from untreated Parkinson's disease patients. Grupo-Centro de Trastornos del MovimientoM A Martín, J A Molina, F J Jiménez-Jiménez, et al.
Clinical Genetics|February 13, 2001
Resolution of a mispaired secondary structure intermediate could account for a novel micro-insertion/deletion (387 insA/del 8 bp) in the PYGM gene causing McArdle's diseaseM A Martín, J C Rubio, A García, et al.
Pageof 13

Showing results (61-70 of 121) with videos related to

Sort By:
Pageof 13
Anales Espanoles De Pediatria|January 1, 1993
[Mitochondrial myopathy caused by complex III and IV deficiency. A familial case]M Castro-Gago, I Novo-Rodríguez, T García Caballero, et al.
Journal of the Neurological Sciences|January 8, 1999
Myophosphorylase deficiency associated with a defect in complex I of the mitochondrial respiratory chainJ C Rubio, M A Martín, J Bautista, et al.
Revista De Neurologia|July 2, 2008
[Association between autistic spectrum and mitochondrial pathology]M Castro-Gago, O Blanco-Barca, C Gómez-Lado, et al.
Neurology|August 1, 1997
Leigh syndrome associated with the T9176C mutation in the ATPase 6 gene of mitochondrial DNAY Campos, M A Martín, J C Rubio, et al.
Revista De Neurologia|September 20, 2001
[MELAS syndrome masquerading as herpes encephalitis: genetic diagnosis]M de Toledo, J Díaz-Guzmán, D A Pérez-Martínez, et al.
Journal of the Neurological Sciences|November 10, 2001
Mitochondrial DNA point mutation in the COI gene in a patient with McArdle's diseaseI Aguilera, J R García-Lozano, A Muñoz, et al.
Neuromuscular Disorders : NMD|September 21, 2000
A mitochondrial tRNA(Lys) gene mutation (T8316C) in a patient with mitochondrial myopathy, lactic acidosis, and stroke-like episodesY Campos, G Lorenzo, M A Martín, et al.
The Journal of Pediatrics|November 1, 1994
Encephalopathy, petechiae, and acrocyanosis with ethylmalonic aciduria associated with muscle cytochrome c oxidase deficiencyM T García-Silva, Y Campos, A Ribes, et al.
Neurology|May 1, 1996
Respiratory-chain enzyme activities in isolated mitochondria of lymphocytes from untreated Parkinson's disease patients. Grupo-Centro de Trastornos del MovimientoM A Martín, J A Molina, F J Jiménez-Jiménez, et al.
Clinical Genetics|February 13, 2001
Resolution of a mispaired secondary structure intermediate could account for a novel micro-insertion/deletion (387 insA/del 8 bp) in the PYGM gene causing McArdle's diseaseM A Martín, J C Rubio, A García, et al.
Pageof 13