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

Y Campos

Showing results (21-30 of 121) with videos related to

Pageof 13
Sort By:
Neurologia (Barcelona, Spain)|March 17, 2007
[Hepatomioneuropathy secondary to mitochondrial DNA depletion]M O Blanco-Barca, C Gómez-Lado, Y Campos-González, et al.
Muscle & Nerve|February 1, 1996
Sporadic MERRF/MELAS overlap syndrome associated with the 3243 tRNA(Leu(UUR)) mutation of mitochondrial DNAY Campos, M A Martin, G Lorenzo, et al.
Journal of Food Science and Technology|July 4, 2025
Inclusion of endophytes in hydroponic cultivation of basils enhances hydroxycinnamic acid levels and antioxidant capacityGabriela Y Campos Espinosa, Patricia Dörr de Quadros, Roberta R Fulthorpe, et al.
Journal of Inherited Metabolic Disease|January 1, 1994
Variable clinical expression associated with the mutation 3243 np of mitochondrial DNAY Campos, J Bautista, E Gutierrez-Rivas, et al.
Journal of Inherited Metabolic Disease|January 1, 1996
Clinical variability associated with the mutation at nucleotide position 8344 of the mitochondrial DNAY Campos, M A Martín, J Vaamonde, et al.
Pediatric Neurology|July 1, 1995
Mitochondrial DNA deletion in a patient with mitochondrial myopathy, lactic acidosis, and stroke-like episodes (MELAS) and Fanconi's syndromeY Campos, T Garcia-Silva, C R Barrionuevo, et al.
FEBS Letters|March 14, 1994
Effects of L-carnitine on the pyruvate dehydrogenase complex and carnitine palmitoyl transferase activities in muscle of endurance athletesJ Arenas, R Huertas, Y Campos, et al.
Muscle & Nerve|December 11, 1999
A missense mutation W797R in the myophosphorylase gene in a Spanish patient with McArdle's diseaseJ C Rubio, M A Martín, Y Campos, et al.
Human Mutation|February 19, 2000
Two homozygous mutations (R193W and 794/795 delAA) in the myophosphorylase gene in a patient with McArdle's diseaseM A Martín, J C Rubio, Y Campos, et al.
Journal of Inherited Metabolic Disease|January 1, 1996
Multiple deletions of mitochondrial DNA in muscle from a patient with benign progressive external ophthalmoplegiaY Campos, M A Martín, J C Rubio, et al.
Pageof 13

Showing results (21-30 of 121) with videos related to

Sort By:
Pageof 13
Neurologia (Barcelona, Spain)|March 17, 2007
[Hepatomioneuropathy secondary to mitochondrial DNA depletion]M O Blanco-Barca, C Gómez-Lado, Y Campos-González, et al.
Muscle & Nerve|February 1, 1996
Sporadic MERRF/MELAS overlap syndrome associated with the 3243 tRNA(Leu(UUR)) mutation of mitochondrial DNAY Campos, M A Martin, G Lorenzo, et al.
Journal of Food Science and Technology|July 4, 2025
Inclusion of endophytes in hydroponic cultivation of basils enhances hydroxycinnamic acid levels and antioxidant capacityGabriela Y Campos Espinosa, Patricia Dörr de Quadros, Roberta R Fulthorpe, et al.
Journal of Inherited Metabolic Disease|January 1, 1994
Variable clinical expression associated with the mutation 3243 np of mitochondrial DNAY Campos, J Bautista, E Gutierrez-Rivas, et al.
Journal of Inherited Metabolic Disease|January 1, 1996
Clinical variability associated with the mutation at nucleotide position 8344 of the mitochondrial DNAY Campos, M A Martín, J Vaamonde, et al.
Pediatric Neurology|July 1, 1995
Mitochondrial DNA deletion in a patient with mitochondrial myopathy, lactic acidosis, and stroke-like episodes (MELAS) and Fanconi's syndromeY Campos, T Garcia-Silva, C R Barrionuevo, et al.
FEBS Letters|March 14, 1994
Effects of L-carnitine on the pyruvate dehydrogenase complex and carnitine palmitoyl transferase activities in muscle of endurance athletesJ Arenas, R Huertas, Y Campos, et al.
Muscle & Nerve|December 11, 1999
A missense mutation W797R in the myophosphorylase gene in a Spanish patient with McArdle's diseaseJ C Rubio, M A Martín, Y Campos, et al.
Human Mutation|February 19, 2000
Two homozygous mutations (R193W and 794/795 delAA) in the myophosphorylase gene in a patient with McArdle's diseaseM A Martín, J C Rubio, Y Campos, et al.
Journal of Inherited Metabolic Disease|January 1, 1996
Multiple deletions of mitochondrial DNA in muscle from a patient with benign progressive external ophthalmoplegiaY Campos, M A Martín, J C Rubio, et al.
Pageof 13