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L Andreu

Showing results (221-230 of 313) with videos related to

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Revista Espanola De Anestesiologia Y Reanimacion|July 1, 1987
[Respiratory depression in the newborn due to a congenital anomaly in plasma cholinesterase]F Gómez Armenta, M S Carrasco Jiménez, A Ruz Ortiz, et al.
The Journal of Biological Chemistry|December 26, 2001
Altered thymidine metabolism due to defects of thymidine phosphorylaseAntonella Spinazzola, Ramon Marti, Ichizo Nishino, et al.
Genes, Brain, and Behavior|October 15, 2013
Identification and biochemical characterization of the novel mutation m.8839G>C in the mitochondrial ATP6 gene associated with NARP syndromeA Blanco-Grau, I Bonaventura-Ibars, J Coll-Cantí, 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.
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.
Journal of Medical Genetics|March 3, 2009
Novel mutations in patients with McArdle disease by analysis of skeletal muscle mRNAI García-Consuegra, J C Rubio, G Nogales-Gadea, 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.
Archives of Neurology|February 19, 2000
A novel missense mutation (W797R) in the myophosphorylase gene in Spanish patients with McArdle diseaseR Fernández, C Navarro, A L Andreu, et al.
Neurology|April 12, 2003
Reversion of mtDNA depletion in a patient with TK2 deficiencyM R Vilà, T Segovia-Silvestre, J Gámez, et al.
Pageof 32

Showing results (221-230 of 313) with videos related to

Sort By:
Pageof 32
Revista Espanola De Anestesiologia Y Reanimacion|July 1, 1987
[Respiratory depression in the newborn due to a congenital anomaly in plasma cholinesterase]F Gómez Armenta, M S Carrasco Jiménez, A Ruz Ortiz, et al.
The Journal of Biological Chemistry|December 26, 2001
Altered thymidine metabolism due to defects of thymidine phosphorylaseAntonella Spinazzola, Ramon Marti, Ichizo Nishino, et al.
Genes, Brain, and Behavior|October 15, 2013
Identification and biochemical characterization of the novel mutation m.8839G>C in the mitochondrial ATP6 gene associated with NARP syndromeA Blanco-Grau, I Bonaventura-Ibars, J Coll-Cantí, 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.
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.
Journal of Medical Genetics|March 3, 2009
Novel mutations in patients with McArdle disease by analysis of skeletal muscle mRNAI García-Consuegra, J C Rubio, G Nogales-Gadea, 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.
Archives of Neurology|February 19, 2000
A novel missense mutation (W797R) in the myophosphorylase gene in Spanish patients with McArdle diseaseR Fernández, C Navarro, A L Andreu, et al.
Neurology|April 12, 2003
Reversion of mtDNA depletion in a patient with TK2 deficiencyM R Vilà, T Segovia-Silvestre, J Gámez, et al.
Pageof 32