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Volker Straub

Showing results (241-250 of 374) with videos related to

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Neuromuscular Disorders : NMD|November 16, 2019
MYO-MRI diagnostic protocols in genetic myopathiesJodi Warman Chardon, Jordi Díaz-Manera, Giorgio Tasca, et al.
Neuromuscular Disorders : NMD|June 29, 2025
Levels of exercise exposure among people living with neuromuscular disorders: lessons learned from real-world dataMark Richardson, Virginie Kinet, Karen Wong, et al.
Muscle & Nerve|May 4, 2022
Comparison of strength testing modalities in dysferlinopathyNatalie F Reash, Meredith K James, Lindsay N Alfano, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|April 4, 2014
Two recurrent mutations are associated with GNE myopathy in the North of BritainAmina Chaouch, Kathryn M Brennan, Judith Hudson, et al.
Human Gene Therapy|December 1, 2022
T Cell Responses to Dystrophin in a Natural History Study of Duchenne Muscular DystrophyKaren Anthony, Pierpaolo Ala, Francesco Catapano, et al.
Acta Neuropathologica|October 20, 2022
Loss of function variants in DNAJB4 cause a myopathy with early respiratory failureConrad C Weihl, Ana Töpf, Rocio Bengoechea, et al.
Plos One|August 23, 2013
Quantitative muscle MRI as an assessment tool for monitoring disease progression in LGMD2I: a multicentre longitudinal studyTracey A Willis, Kieren G Hollingsworth, Anna Coombs, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|November 28, 2017
Limb girdle muscular dystrophy due to mutations in <i>POMT2</i>Sofie Thurø Østergaard, Katherine Johnson, Tanya Stojkovic, et al.
Medrxiv : the Preprint Server for Health Sciences|January 10, 2024
Loss of Function of the Cytoplasmic Fe-S Assembly Protein CIAO1 Causes a Neuromuscular Disorder with Compromise of Nucleocytoplasmic Fe-S EnzymesNunziata Maio, Rotem Orbach, Irina Zaharieva, et al.
The Lancet. Neurology|June 16, 2016
Stakeholder cooperation to overcome challenges in orphan medicine development: the example of Duchenne muscular dystrophyVolker Straub, Pavel Balabanov, Kate Bushby, et al.
Pageof 38

Showing results (241-250 of 374) with videos related to

Sort By:
Pageof 38
Neuromuscular Disorders : NMD|November 16, 2019
MYO-MRI diagnostic protocols in genetic myopathiesJodi Warman Chardon, Jordi Díaz-Manera, Giorgio Tasca, et al.
Neuromuscular Disorders : NMD|June 29, 2025
Levels of exercise exposure among people living with neuromuscular disorders: lessons learned from real-world dataMark Richardson, Virginie Kinet, Karen Wong, et al.
Muscle & Nerve|May 4, 2022
Comparison of strength testing modalities in dysferlinopathyNatalie F Reash, Meredith K James, Lindsay N Alfano, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|April 4, 2014
Two recurrent mutations are associated with GNE myopathy in the North of BritainAmina Chaouch, Kathryn M Brennan, Judith Hudson, et al.
Human Gene Therapy|December 1, 2022
T Cell Responses to Dystrophin in a Natural History Study of Duchenne Muscular DystrophyKaren Anthony, Pierpaolo Ala, Francesco Catapano, et al.
Acta Neuropathologica|October 20, 2022
Loss of function variants in DNAJB4 cause a myopathy with early respiratory failureConrad C Weihl, Ana Töpf, Rocio Bengoechea, et al.
Plos One|August 23, 2013
Quantitative muscle MRI as an assessment tool for monitoring disease progression in LGMD2I: a multicentre longitudinal studyTracey A Willis, Kieren G Hollingsworth, Anna Coombs, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|November 28, 2017
Limb girdle muscular dystrophy due to mutations in <i>POMT2</i>Sofie Thurø Østergaard, Katherine Johnson, Tanya Stojkovic, et al.
Medrxiv : the Preprint Server for Health Sciences|January 10, 2024
Loss of Function of the Cytoplasmic Fe-S Assembly Protein CIAO1 Causes a Neuromuscular Disorder with Compromise of Nucleocytoplasmic Fe-S EnzymesNunziata Maio, Rotem Orbach, Irina Zaharieva, et al.
The Lancet. Neurology|June 16, 2016
Stakeholder cooperation to overcome challenges in orphan medicine development: the example of Duchenne muscular dystrophyVolker Straub, Pavel Balabanov, Kate Bushby, et al.
Pageof 38