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Antoni L Andreu

Showing results (31-40 of 77) with videos related to

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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.
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.
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.
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.
Stroke|November 8, 2003
Safety profile of tissue plasminogen activator treatment among stroke patients carrying a common polymorphism (C-1562T) in the promoter region of the matrix metalloproteinase-9 geneJoan Montaner, Israel Fernández-Cadenas, Carlos A Molina, et al.
The Journal of Pediatrics|January 15, 2004
Mitochondrial DNA abnormalities and autistic spectrum disordersRoser Pons, Antoni L Andreu, Nicoletta Checcarelli, et al.
Journal of Medical Case Reports|August 30, 2008
Impaired expression of mitochondrial and adipogenic genes in adipose tissue from a patient with acquired partial lipodystrophy (Barraquer-Simons syndrome): a case reportJordi P Guallar, Ricardo Rojas-Garcia, Elena Garcia-Arumi, et al.
Neuroscience Letters|July 17, 2007
Genotype modulators of clinical severity in McArdle diseaseJuan C Rubio, Félix Gómez-Gallego, Catalina Santiago, et al.
Neuromuscular Disorders : NMD|February 5, 2013
Identification of the novel mutation m.5658T>C in the mitochondrial tRNA(Asn) gene in a patient with myopathy, bilateral ptosis and ophthalmoparesisTomàs Pinós, Maria Jesús Melià, Nicolau Ortiz, et al.
Pageof 8

Showing results (31-40 of 77) with videos related to

Sort By:
Pageof 8
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.
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.
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.
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.
Stroke|November 8, 2003
Safety profile of tissue plasminogen activator treatment among stroke patients carrying a common polymorphism (C-1562T) in the promoter region of the matrix metalloproteinase-9 geneJoan Montaner, Israel Fernández-Cadenas, Carlos A Molina, et al.
The Journal of Pediatrics|January 15, 2004
Mitochondrial DNA abnormalities and autistic spectrum disordersRoser Pons, Antoni L Andreu, Nicoletta Checcarelli, et al.
Journal of Medical Case Reports|August 30, 2008
Impaired expression of mitochondrial and adipogenic genes in adipose tissue from a patient with acquired partial lipodystrophy (Barraquer-Simons syndrome): a case reportJordi P Guallar, Ricardo Rojas-Garcia, Elena Garcia-Arumi, et al.
Neuroscience Letters|July 17, 2007
Genotype modulators of clinical severity in McArdle diseaseJuan C Rubio, Félix Gómez-Gallego, Catalina Santiago, et al.
Neuromuscular Disorders : NMD|February 5, 2013
Identification of the novel mutation m.5658T>C in the mitochondrial tRNA(Asn) gene in a patient with myopathy, bilateral ptosis and ophthalmoparesisTomàs Pinós, Maria Jesús Melià, Nicolau Ortiz, et al.
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