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L Andreu

Showing results (211-220 of 313) with videos related to

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Annals of Neurology|June 9, 1999
Exercise intolerance due to a nonsense mutation in the mtDNA ND4 geneA L Andreu, K Tanji, C Bruno, et al.
Human Molecular Genetics|August 11, 2011
'Progress' renders detrimental an ancient mitochondrial DNA genetic variantDavid Pacheu-Grau, Aurora Gómez-Durán, Ester López-Gallardo, et al.
Neurology|October 27, 2004
Lack of gastrointestinal symptoms in a 60-year-old patient with MNGIEM A Martín, A Blázquez, R Martí, et al.
Journal of the Neurological Sciences|July 13, 1999
A new mitochondrial DNA mutation (A3288G) in the tRNA(Leu(UUR)) gene associated with familial myopathyG M Hadjigeorgiou, S H Kim, K H Fischbeck, et al.
Annals of Neurology|October 2, 2003
Bilateral striatal necrosis associated with a novel mutation in the mitochondrial ND6 geneAbelardo Solano, Manuel Roig, Cristofol Vives-Bauza, et al.
Human Gene Therapy|March 24, 2016
Long-Term Restoration of Thymidine Phosphorylase Function and Nucleoside Homeostasis Using Hematopoietic Gene Therapy in a Murine Model of Mitochondrial Neurogastrointestinal EncephalomyopathyJavier Torres-Torronteras, Raquel Cabrera-Pérez, Ignasi Barba, et al.
Pediatric Research|April 28, 2010
Hearing loss in a patient with the myopathic form of mitochondrial DNA depletion syndrome and a novel mutation in the TK2 geneRamon Martí, Andrés Nascimento, Jaume Colomer, et al.
Revista De Neurologia|September 19, 2007
[Private mutations in the myophosphorylase gene: the first case in a patient of Latin American descent]I Fernandez-Cadenas, G Nogales-Gadea, D Llige, et al.
Pediatric Nephrology (Berlin, Germany)|May 11, 2004
De Toni-Debré-Fanconi syndrome due to a palindrome-flanked deletion in mitochondrial DNAAbelardo Solano, Giovanna Russo, Ana Playán, et al.
Human Genetics|March 26, 2009
Novel human pathological mutations. Gene symbol: PYGM. Disease: McArdle diseaseInes Garcia-Consuegra, J C Rubio, G Nogales-Gadea, et al.
Pageof 32

Showing results (211-220 of 313) with videos related to

Sort By:
Pageof 32
Annals of Neurology|June 9, 1999
Exercise intolerance due to a nonsense mutation in the mtDNA ND4 geneA L Andreu, K Tanji, C Bruno, et al.
Human Molecular Genetics|August 11, 2011
'Progress' renders detrimental an ancient mitochondrial DNA genetic variantDavid Pacheu-Grau, Aurora Gómez-Durán, Ester López-Gallardo, et al.
Neurology|October 27, 2004
Lack of gastrointestinal symptoms in a 60-year-old patient with MNGIEM A Martín, A Blázquez, R Martí, et al.
Journal of the Neurological Sciences|July 13, 1999
A new mitochondrial DNA mutation (A3288G) in the tRNA(Leu(UUR)) gene associated with familial myopathyG M Hadjigeorgiou, S H Kim, K H Fischbeck, et al.
Annals of Neurology|October 2, 2003
Bilateral striatal necrosis associated with a novel mutation in the mitochondrial ND6 geneAbelardo Solano, Manuel Roig, Cristofol Vives-Bauza, et al.
Human Gene Therapy|March 24, 2016
Long-Term Restoration of Thymidine Phosphorylase Function and Nucleoside Homeostasis Using Hematopoietic Gene Therapy in a Murine Model of Mitochondrial Neurogastrointestinal EncephalomyopathyJavier Torres-Torronteras, Raquel Cabrera-Pérez, Ignasi Barba, et al.
Pediatric Research|April 28, 2010
Hearing loss in a patient with the myopathic form of mitochondrial DNA depletion syndrome and a novel mutation in the TK2 geneRamon Martí, Andrés Nascimento, Jaume Colomer, et al.
Revista De Neurologia|September 19, 2007
[Private mutations in the myophosphorylase gene: the first case in a patient of Latin American descent]I Fernandez-Cadenas, G Nogales-Gadea, D Llige, et al.
Pediatric Nephrology (Berlin, Germany)|May 11, 2004
De Toni-Debré-Fanconi syndrome due to a palindrome-flanked deletion in mitochondrial DNAAbelardo Solano, Giovanna Russo, Ana Playán, et al.
Human Genetics|March 26, 2009
Novel human pathological mutations. Gene symbol: PYGM. Disease: McArdle diseaseInes Garcia-Consuegra, J C Rubio, G Nogales-Gadea, et al.
Pageof 32