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L Andreu

Showing results (191-200 of 313) with videos related to

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Neuromuscular Disorders : NMD|November 2, 1999
Manifesting heterozygotes in a Japanese family with a novel mutation in the muscle-specific phosphoglycerate mutase (PGAM-M) geneG M Hadjigeorgiou, N Kawashima, C Bruno, et al.
European Journal of Pain (London, England)|June 12, 2010
Pain relief by applying transcutaneous electrical nerve stimulation (TENS) during unsedated colonoscopy: a randomized double-blind placebo-controlled trialJ J Amer-Cuenca, C Goicoechea, A Girona-López, et al.
Mitochondrion|September 4, 2010
A novel mutation in the mitochondrial tRNA(Ala) gene (m.5636T>C) in a patient with progressive external ophthalmoplegiaTomàs Pinós, Mario Marotta, Eduard Gallardo, et al.
Archives of Neurology|December 19, 2006
Novel mutation in the PYGM gene resulting in McArdle diseaseJuan C Rubio, Alejandro Lucia, Israel Fernández-Cadenas, et al.
The British Journal of Surgery|June 1, 1995
Clinical improvement after liver transplantation for type I familial amyloid polyneuropathyP Parrilla, P Ramirez, F S Bueno, et al.
Disease Models & Mechanisms|March 13, 2015
Sodium valproate increases the brain isoform of glycogen phosphorylase: looking for a compensation mechanism in McArdle disease using a mouse primary skeletal-muscle culture in vitroNoemí de Luna, Astrid Brull, Josep Maria Guiu, et al.
The Journal of Physiology|April 16, 2015
Phenotype consequences of myophosphorylase dysfunction: insights from the McArdle mouse modelAstrid Brull, Noemí de Luna, Albert Blanco-Grau, et al.
Journal of Personalized Medicine|July 27, 2022
Evaluating Translational Methods for Personalized Medicine-A Scoping ReviewVibeke Fosse, Emanuela Oldoni, Chiara Gerardi, et al.
Neurology|July 23, 1998
Molecular genetic analysis of McArdle's disease in Spanish patientsA L Andreu, C Bruno, J Gamez, et al.
Neurology|September 15, 2006
Infusion of platelets transiently reduces nucleoside overload in MNGIEM C Lara, B Weiss, I Illa, et al.
Pageof 32

Showing results (191-200 of 313) with videos related to

Sort By:
Pageof 32
Neuromuscular Disorders : NMD|November 2, 1999
Manifesting heterozygotes in a Japanese family with a novel mutation in the muscle-specific phosphoglycerate mutase (PGAM-M) geneG M Hadjigeorgiou, N Kawashima, C Bruno, et al.
European Journal of Pain (London, England)|June 12, 2010
Pain relief by applying transcutaneous electrical nerve stimulation (TENS) during unsedated colonoscopy: a randomized double-blind placebo-controlled trialJ J Amer-Cuenca, C Goicoechea, A Girona-López, et al.
Mitochondrion|September 4, 2010
A novel mutation in the mitochondrial tRNA(Ala) gene (m.5636T>C) in a patient with progressive external ophthalmoplegiaTomàs Pinós, Mario Marotta, Eduard Gallardo, et al.
Archives of Neurology|December 19, 2006
Novel mutation in the PYGM gene resulting in McArdle diseaseJuan C Rubio, Alejandro Lucia, Israel Fernández-Cadenas, et al.
The British Journal of Surgery|June 1, 1995
Clinical improvement after liver transplantation for type I familial amyloid polyneuropathyP Parrilla, P Ramirez, F S Bueno, et al.
Disease Models & Mechanisms|March 13, 2015
Sodium valproate increases the brain isoform of glycogen phosphorylase: looking for a compensation mechanism in McArdle disease using a mouse primary skeletal-muscle culture in vitroNoemí de Luna, Astrid Brull, Josep Maria Guiu, et al.
The Journal of Physiology|April 16, 2015
Phenotype consequences of myophosphorylase dysfunction: insights from the McArdle mouse modelAstrid Brull, Noemí de Luna, Albert Blanco-Grau, et al.
Journal of Personalized Medicine|July 27, 2022
Evaluating Translational Methods for Personalized Medicine-A Scoping ReviewVibeke Fosse, Emanuela Oldoni, Chiara Gerardi, et al.
Neurology|July 23, 1998
Molecular genetic analysis of McArdle's disease in Spanish patientsA L Andreu, C Bruno, J Gamez, et al.
Neurology|September 15, 2006
Infusion of platelets transiently reduces nucleoside overload in MNGIEM C Lara, B Weiss, I Illa, et al.
Pageof 32