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Volker Straub

Showing results (231-240 of 374) with videos related to

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Neuromuscular Disorders : NMD|September 18, 2012
Muscle MRI findings in limb girdle muscular dystrophy type 2LAnna Sarkozy, Marcus Deschauer, Robert-Yves Carlier, et al.
Proteomics. Clinical Applications|January 25, 2014
Fibronectin is a serum biomarker for Duchenne muscular dystrophyF Cynthia Martin, Monika Hiller, Pietro Spitali, et al.
Brain : a Journal of Neurology|September 20, 2007
Refining genotype phenotype correlations in muscular dystrophies with defective glycosylation of dystroglycanCaroline Godfrey, Emma Clement, Rachael Mein, et al.
Lancet (London, England)|July 26, 2011
Exon skipping and dystrophin restoration in patients with Duchenne muscular dystrophy after systemic phosphorodiamidate morpholino oligomer treatment: an open-label, phase 2, dose-escalation studySebahattin Cirak, Virginia Arechavala-Gomeza, Michela Guglieri, et al.
American Journal of Human Genetics|October 18, 2016
Association Study of Exon Variants in the NF-κB and TGFβ Pathways Identifies CD40 as a Modifier of Duchenne Muscular DystrophyLuca Bello, Kevin M Flanigan, Robert B Weiss, et al.
Muscle & Nerve|October 4, 2021
Genotype-related respiratory progression in Duchenne muscular dystrophy-A multicenter international studyFederica Trucco, Deborah Ridout, Joana Domingos, et al.
Neurology. Genetics|May 24, 2019
Muscular dystrophy with arrhythmia caused by loss-of-function mutations in <i>BVES</i>Willem De Ridder, Isabelle Nelson, Bob Asselbergh, et al.
Annals of Clinical and Translational Neurology|June 19, 2019
Natural history of limb girdle muscular dystrophy R9 over 6 years: searching for trial endpointsAlexander P Murphy, Jasper Morrow, Julia R Dahlqvist, et al.
European Journal of Human Genetics : EJHG|December 4, 2008
In-frame deletion in the seventh immunoglobulin-like repeat of filamin C in a family with myofibrillar myopathyAlexey Shatunov, Montse Olivé, Zagaa Odgerel, et al.
Annals of Clinical and Translational Neurology|October 7, 2025
SNUPN-Related Muscular Dystrophy: Novel Phenotypic, Pathological and Functional Protein InsightsNuria Muelas, Pablo Iruzubieta, Alberto Damborenea, et al.
Pageof 38

Showing results (231-240 of 374) with videos related to

Sort By:
Pageof 38
Neuromuscular Disorders : NMD|September 18, 2012
Muscle MRI findings in limb girdle muscular dystrophy type 2LAnna Sarkozy, Marcus Deschauer, Robert-Yves Carlier, et al.
Proteomics. Clinical Applications|January 25, 2014
Fibronectin is a serum biomarker for Duchenne muscular dystrophyF Cynthia Martin, Monika Hiller, Pietro Spitali, et al.
Brain : a Journal of Neurology|September 20, 2007
Refining genotype phenotype correlations in muscular dystrophies with defective glycosylation of dystroglycanCaroline Godfrey, Emma Clement, Rachael Mein, et al.
Lancet (London, England)|July 26, 2011
Exon skipping and dystrophin restoration in patients with Duchenne muscular dystrophy after systemic phosphorodiamidate morpholino oligomer treatment: an open-label, phase 2, dose-escalation studySebahattin Cirak, Virginia Arechavala-Gomeza, Michela Guglieri, et al.
American Journal of Human Genetics|October 18, 2016
Association Study of Exon Variants in the NF-κB and TGFβ Pathways Identifies CD40 as a Modifier of Duchenne Muscular DystrophyLuca Bello, Kevin M Flanigan, Robert B Weiss, et al.
Muscle & Nerve|October 4, 2021
Genotype-related respiratory progression in Duchenne muscular dystrophy-A multicenter international studyFederica Trucco, Deborah Ridout, Joana Domingos, et al.
Neurology. Genetics|May 24, 2019
Muscular dystrophy with arrhythmia caused by loss-of-function mutations in <i>BVES</i>Willem De Ridder, Isabelle Nelson, Bob Asselbergh, et al.
Annals of Clinical and Translational Neurology|June 19, 2019
Natural history of limb girdle muscular dystrophy R9 over 6 years: searching for trial endpointsAlexander P Murphy, Jasper Morrow, Julia R Dahlqvist, et al.
European Journal of Human Genetics : EJHG|December 4, 2008
In-frame deletion in the seventh immunoglobulin-like repeat of filamin C in a family with myofibrillar myopathyAlexey Shatunov, Montse Olivé, Zagaa Odgerel, et al.
Annals of Clinical and Translational Neurology|October 7, 2025
SNUPN-Related Muscular Dystrophy: Novel Phenotypic, Pathological and Functional Protein InsightsNuria Muelas, Pablo Iruzubieta, Alberto Damborenea, et al.
Pageof 38