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 (71-80 of 93) with videos related to

Pageof 10
Sort By:
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.
American Journal of Human Genetics|August 12, 1999
A stop-codon mutation in the human mtDNA cytochrome c oxidase I gene disrupts the functional structure of complex IVC Bruno, A Martinuzzi, Y Tang, et al.
Neuromuscular Disorders : NMD|June 19, 2001
A new mtDNA mutation in the tRNA(Leu(UUR)) gene associated with ocular myopathyY Campos, J Gámez, A García, et al.
Annals of Neurology|January 23, 1999
A nonsense mutation (G15059A) in the cytochrome b gene in a patient with exercise intolerance and myoglobinuriaA L Andreu, C Bruno, T C Dunne, et al.
Neurology|February 27, 2001
Autosomal dominant limb-girdle muscular dystrophy: a large kindred with evidence for anticipationJ Gamez, C Navarro, A L Andreu, et al.
British Journal of Sports Medicine|July 26, 2006
Exercise capacity in a 78 year old patient with McArdle's disease: it is never too late to start exercisingM Perez, M A Martin, J C Rubio, et al.
The Journal of Pediatrics|June 4, 1999
Infantile encephalopathy associated with the MELAS A3243G mutationC M Sue, C Bruno, A L Andreu, et al.
British Journal of Sports Medicine|June 30, 2006
Mobilisation of mesenchymal cells into blood in response to skeletal muscle injuryM Ramírez, A Lucia, F Gómez-Gallego, et al.
The New England Journal of Medicine|September 30, 1999
Exercise intolerance due to mutations in the cytochrome b gene of mitochondrial DNAA L Andreu, M G Hanna, H Reichmann, et al.
Pageof 10

Showing results (71-80 of 93) with videos related to

Sort By:
Pageof 10
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.
American Journal of Human Genetics|August 12, 1999
A stop-codon mutation in the human mtDNA cytochrome c oxidase I gene disrupts the functional structure of complex IVC Bruno, A Martinuzzi, Y Tang, et al.
Neuromuscular Disorders : NMD|June 19, 2001
A new mtDNA mutation in the tRNA(Leu(UUR)) gene associated with ocular myopathyY Campos, J Gámez, A García, et al.
Annals of Neurology|January 23, 1999
A nonsense mutation (G15059A) in the cytochrome b gene in a patient with exercise intolerance and myoglobinuriaA L Andreu, C Bruno, T C Dunne, et al.
Neurology|February 27, 2001
Autosomal dominant limb-girdle muscular dystrophy: a large kindred with evidence for anticipationJ Gamez, C Navarro, A L Andreu, et al.
British Journal of Sports Medicine|July 26, 2006
Exercise capacity in a 78 year old patient with McArdle's disease: it is never too late to start exercisingM Perez, M A Martin, J C Rubio, et al.
The Journal of Pediatrics|June 4, 1999
Infantile encephalopathy associated with the MELAS A3243G mutationC M Sue, C Bruno, A L Andreu, et al.
British Journal of Sports Medicine|June 30, 2006
Mobilisation of mesenchymal cells into blood in response to skeletal muscle injuryM Ramírez, A Lucia, F Gómez-Gallego, et al.
The New England Journal of Medicine|September 30, 1999
Exercise intolerance due to mutations in the cytochrome b gene of mitochondrial DNAA L Andreu, M G Hanna, H Reichmann, et al.
Pageof 10