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

Andres Nascimento

Showing results (1-10 of 55) with videos related to

Pageof 6
Sort By:
BMC Genomics|February 24, 2010
Comparative gene expression profiling between human cultured myotubes and skeletal muscle tissueFrederic Raymond, Sylviane Métairon, Martin Kussmann, et al.
Plos One|August 19, 2015
DMD Mutations in 576 Dystrophinopathy Families: A Step Forward in Genotype-Phenotype CorrelationsJonas Juan-Mateu, Lidia Gonzalez-Quereda, Maria Jose Rodriguez, et al.
Neuromuscular Disorders : NMD|June 30, 2006
Clinical spectrum of CMT4C disease in patients homozygous for the p.Arg1109X mutation in SH3TC2Jaume Colomer, Rebecca Gooding, Dora Angelicheva, et al.
Neuromuscular Disorders : NMD|December 17, 2016
Digital PCR quantification of miR-30c and miR-181a as serum biomarkers for Duchenne muscular dystrophyMonica Llano-Diez, Carlos Ignacio Ortez, Judit Armas Gay, et al.
Neurology and Therapy|November 3, 2025
Caregiver-reported Patient Experiences with Duchenne Muscular Dystrophy: Qualitative In-trial Interviews 1 Year After Delandistrogene Moxeparvovec in the Pivotal EMBARK TrialIvana Audhya, Alise B Nacson, Katherine Gooch, et al.
Frontiers in Neurology|May 7, 2020
Longitudinal Study of Three microRNAs in Duchenne Muscular Dystrophy and Becker Muscular DystrophySelena Trifunov, Daniel Natera-de Benito, Jesica Maria Exposito Escudero, et al.
Annals of Neurology|December 21, 2005
Cerebral folate deficiency and leukoencephalopathy caused by a mitochondrial DNA deletionMerce Pineda, Aida Ormazabal, Esther López-Gallardo, et al.
Mitochondrion|June 19, 2008
Mitochondrial diseases mimicking neurotransmitter defectsAngels Garcia-Cazorla, Sofia Duarte, Mercedes Serrano, et al.
Neuromuscular Disorders : NMD|January 2, 2017
Homozygous truncating mutation in prenatally expressed skeletal isoform of TTN gene results in arthrogryposis multiplex congenita and myopathy without cardiac involvementAna Fernández-Marmiesse, M Carmen Carrascosa-Romero, Blanca Alfaro Ponce, et al.
Journal of Neuropathology and Experimental Neurology|September 15, 2012
Muscle fiber atrophy and regeneration coexist in collagen VI-deficient human muscle: role of calpain-3 and nuclear factor-κB signalingSonia Paco, Isidre Ferrer, Cristina Jou, et al.
Pageof 6

Showing results (1-10 of 55) with videos related to

Sort By:
Pageof 6
BMC Genomics|February 24, 2010
Comparative gene expression profiling between human cultured myotubes and skeletal muscle tissueFrederic Raymond, Sylviane Métairon, Martin Kussmann, et al.
Plos One|August 19, 2015
DMD Mutations in 576 Dystrophinopathy Families: A Step Forward in Genotype-Phenotype CorrelationsJonas Juan-Mateu, Lidia Gonzalez-Quereda, Maria Jose Rodriguez, et al.
Neuromuscular Disorders : NMD|June 30, 2006
Clinical spectrum of CMT4C disease in patients homozygous for the p.Arg1109X mutation in SH3TC2Jaume Colomer, Rebecca Gooding, Dora Angelicheva, et al.
Neuromuscular Disorders : NMD|December 17, 2016
Digital PCR quantification of miR-30c and miR-181a as serum biomarkers for Duchenne muscular dystrophyMonica Llano-Diez, Carlos Ignacio Ortez, Judit Armas Gay, et al.
Neurology and Therapy|November 3, 2025
Caregiver-reported Patient Experiences with Duchenne Muscular Dystrophy: Qualitative In-trial Interviews 1 Year After Delandistrogene Moxeparvovec in the Pivotal EMBARK TrialIvana Audhya, Alise B Nacson, Katherine Gooch, et al.
Frontiers in Neurology|May 7, 2020
Longitudinal Study of Three microRNAs in Duchenne Muscular Dystrophy and Becker Muscular DystrophySelena Trifunov, Daniel Natera-de Benito, Jesica Maria Exposito Escudero, et al.
Annals of Neurology|December 21, 2005
Cerebral folate deficiency and leukoencephalopathy caused by a mitochondrial DNA deletionMerce Pineda, Aida Ormazabal, Esther López-Gallardo, et al.
Mitochondrion|June 19, 2008
Mitochondrial diseases mimicking neurotransmitter defectsAngels Garcia-Cazorla, Sofia Duarte, Mercedes Serrano, et al.
Neuromuscular Disorders : NMD|January 2, 2017
Homozygous truncating mutation in prenatally expressed skeletal isoform of TTN gene results in arthrogryposis multiplex congenita and myopathy without cardiac involvementAna Fernández-Marmiesse, M Carmen Carrascosa-Romero, Blanca Alfaro Ponce, et al.
Journal of Neuropathology and Experimental Neurology|September 15, 2012
Muscle fiber atrophy and regeneration coexist in collagen VI-deficient human muscle: role of calpain-3 and nuclear factor-κB signalingSonia Paco, Isidre Ferrer, Cristina Jou, et al.
Pageof 6