Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

A L Andreu

Showing results (51-60 of 93) with videos related to

Pageof 10
Sort By:
The European Respiratory Journal|July 2, 2011
Effect of an ambulatory diagnostic and treatment programme in patients with sleep apnoeaA L Andreu, E Chiner, J N Sancho-Chust, et al.
Biochemical and Biophysical Research Communications|December 5, 1998
Reduced mitochondrial DNA transcription in senescent rat heartA L Andreu, M A Arbos, A Perez-Martos, et al.
Neuroscience Letters|December 29, 2007
McArdle disease: another systemic low-inflammation disorder?Alejandro Lucia, Lucille Smith, Melissa Naidoo, et al.
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.
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.
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.
Pageof 10

Showing results (51-60 of 93) with videos related to

Sort By:
Pageof 10
The European Respiratory Journal|July 2, 2011
Effect of an ambulatory diagnostic and treatment programme in patients with sleep apnoeaA L Andreu, E Chiner, J N Sancho-Chust, et al.
Biochemical and Biophysical Research Communications|December 5, 1998
Reduced mitochondrial DNA transcription in senescent rat heartA L Andreu, M A Arbos, A Perez-Martos, et al.
Neuroscience Letters|December 29, 2007
McArdle disease: another systemic low-inflammation disorder?Alejandro Lucia, Lucille Smith, Melissa Naidoo, et al.
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.
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.
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.
Pageof 10