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L Andreu

Showing results (201-210 of 313) with videos related to

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Archives of Neurology|April 13, 2005
Leigh syndrome associated with mitochondrial complex I deficiency due to a novel mutation in the NDUFS1 geneMiguel A Martín, Alberto Blázquez, Luis G Gutierrez-Solana, et al.
Neurology|November 18, 1998
Missense mutation in the mtDNA cytochrome b gene in a patient with myopathyA L Andreu, C Bruno, S Shanske, et al.
Revista De Neurologia|July 23, 2002
[Leigh syndrome resulting from a de novo mitochondrial DNA mutation (T8993G)]A Playán, A Solano-Palacios, J B González de la Rosa, et al.
Neuromuscular Disorders : NMD|October 4, 2005
Increased muscle nucleoside levels associated with a novel frameshift mutation in the thymidine phosphorylase gene in a Spanish patient with MNGIEA Blazquez, M A Martín, M C Lara, et al.
Neurology|July 23, 1998
Familial multiple symmetric lipomatosis associated with the A8344G mutation of mitochondrial DNAJ Gámez, A Playán, A L Andreu, et al.
Human Mutation|January 16, 2007
A proposed molecular diagnostic flowchart for myophosphorylase deficiency (McArdle disease) in blood samples from Spanish patientsJuan C Rubio, Ines Garcia-Consuegra, Gisela Nogales-Gadea, et al.
Archivos De Bronconeumologia|June 24, 2026
Mitochondrial Dysfunction and Telomeric Shortening as Long-term Complications After COVID-19Alba Mulet, Jaime Signes-Costa, Estrella Fernández-Fabrellas, et al.
Acta Neuropathologica|December 10, 2002
The A8344G mutation in mitochondrial DNA associated with stroke-like episodes and gastrointestinal dysfunctionKurenai Tanji, Josep Gamez, Carles Cervera, et al.
Neurology|August 15, 2002
Phenotypic variability in a Spanish family with MNGIEJ Gamez, C Ferreiro, M L Accarino, et al.
British Journal of Sports Medicine|September 27, 2006
Can patients with McArdle's disease run?M Pérez, M Moran, C Cardona, et al.
Pageof 32

Showing results (201-210 of 313) with videos related to

Sort By:
Pageof 32
Archives of Neurology|April 13, 2005
Leigh syndrome associated with mitochondrial complex I deficiency due to a novel mutation in the NDUFS1 geneMiguel A Martín, Alberto Blázquez, Luis G Gutierrez-Solana, et al.
Neurology|November 18, 1998
Missense mutation in the mtDNA cytochrome b gene in a patient with myopathyA L Andreu, C Bruno, S Shanske, et al.
Revista De Neurologia|July 23, 2002
[Leigh syndrome resulting from a de novo mitochondrial DNA mutation (T8993G)]A Playán, A Solano-Palacios, J B González de la Rosa, et al.
Neuromuscular Disorders : NMD|October 4, 2005
Increased muscle nucleoside levels associated with a novel frameshift mutation in the thymidine phosphorylase gene in a Spanish patient with MNGIEA Blazquez, M A Martín, M C Lara, et al.
Neurology|July 23, 1998
Familial multiple symmetric lipomatosis associated with the A8344G mutation of mitochondrial DNAJ Gámez, A Playán, A L Andreu, et al.
Human Mutation|January 16, 2007
A proposed molecular diagnostic flowchart for myophosphorylase deficiency (McArdle disease) in blood samples from Spanish patientsJuan C Rubio, Ines Garcia-Consuegra, Gisela Nogales-Gadea, et al.
Archivos De Bronconeumologia|June 24, 2026
Mitochondrial Dysfunction and Telomeric Shortening as Long-term Complications After COVID-19Alba Mulet, Jaime Signes-Costa, Estrella Fernández-Fabrellas, et al.
Acta Neuropathologica|December 10, 2002
The A8344G mutation in mitochondrial DNA associated with stroke-like episodes and gastrointestinal dysfunctionKurenai Tanji, Josep Gamez, Carles Cervera, et al.
Neurology|August 15, 2002
Phenotypic variability in a Spanish family with MNGIEJ Gamez, C Ferreiro, M L Accarino, et al.
British Journal of Sports Medicine|September 27, 2006
Can patients with McArdle's disease run?M Pérez, M Moran, C Cardona, et al.
Pageof 32