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Tracey Willis

Showing results (21-30 of 40) with videos related to

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Journal of Neurology|May 11, 2016
Design, set-up and utility of the UK facioscapulohumeral muscular dystrophy patient registryTeresinha Evangelista, Libby Wood, Roberto Fernandez-Torron, et al.
Neuromuscular Disorders : NMD|March 5, 2026
Framing childhood-onset facioscapulohumeral dystrophy: from first symptoms to future trialsJildou N Dijkstra, Corrie E Erasmus, Pierre Laurian, et al.
Journal of Neuromuscular Diseases|January 8, 2024
Risdiplam in Spinal Muscular Atrophy: Safety Profile and Use Through The Early Access to Medicine Scheme for the Paediatric Cohort in Great BritainNikki Cornell, Anne-Marie Childs, Elizabeth Wraige, et al.
Acta Neuropathologica Communications|August 29, 2019
Clinical, histological, and genetic characterization of PYROXD1-related myopathyXavière Lornage, Vanessa Schartner, Inès Balbueno, et al.
BMJ Open|December 22, 2018
Randomised placebo-controlled trial of combination ACE inhibitor and beta-blocker therapy to prevent cardiomyopathy in children with Duchenne muscular dystrophy? (DMD Heart Protection Study): a protocol studyJohn P Bourke, Gillian Watson, Francesco Muntoni, et al.
Muscle & Nerve|October 21, 2017
Chronic pain has a strong impact on quality of life in facioscapulohumeral muscular dystrophyGermán Morís, Libby Wood, Roberto FernáNdez-Torrón, et al.
Neuromuscular Disorders : NMD|August 23, 2018
ECEL1 gene related contractural syndrome: Long-term follow-up and update on clinical and pathological aspectsUrielle Ullmann, Luigi D'Argenzio, Shrey Mathur, et al.
Pilot and Feasibility Studies|March 31, 2017
Aquatic therapy for boys with Duchenne muscular dystrophy (DMD): an external pilot randomised controlled trialDaniel Hind, James Parkin, Victoria Whitworth, et al.
Health Technology Assessment (Winchester, England)|June 20, 2017
Aquatic therapy for children with Duchenne muscular dystrophy: a pilot feasibility randomised controlled trial and mixed-methods process evaluationDaniel Hind, James Parkin, Victoria Whitworth, 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.
Pageof 4

Showing results (21-30 of 40) with videos related to

Sort By:
Pageof 4
Journal of Neurology|May 11, 2016
Design, set-up and utility of the UK facioscapulohumeral muscular dystrophy patient registryTeresinha Evangelista, Libby Wood, Roberto Fernandez-Torron, et al.
Neuromuscular Disorders : NMD|March 5, 2026
Framing childhood-onset facioscapulohumeral dystrophy: from first symptoms to future trialsJildou N Dijkstra, Corrie E Erasmus, Pierre Laurian, et al.
Journal of Neuromuscular Diseases|January 8, 2024
Risdiplam in Spinal Muscular Atrophy: Safety Profile and Use Through The Early Access to Medicine Scheme for the Paediatric Cohort in Great BritainNikki Cornell, Anne-Marie Childs, Elizabeth Wraige, et al.
Acta Neuropathologica Communications|August 29, 2019
Clinical, histological, and genetic characterization of PYROXD1-related myopathyXavière Lornage, Vanessa Schartner, Inès Balbueno, et al.
BMJ Open|December 22, 2018
Randomised placebo-controlled trial of combination ACE inhibitor and beta-blocker therapy to prevent cardiomyopathy in children with Duchenne muscular dystrophy? (DMD Heart Protection Study): a protocol studyJohn P Bourke, Gillian Watson, Francesco Muntoni, et al.
Muscle & Nerve|October 21, 2017
Chronic pain has a strong impact on quality of life in facioscapulohumeral muscular dystrophyGermán Morís, Libby Wood, Roberto FernáNdez-Torrón, et al.
Neuromuscular Disorders : NMD|August 23, 2018
ECEL1 gene related contractural syndrome: Long-term follow-up and update on clinical and pathological aspectsUrielle Ullmann, Luigi D'Argenzio, Shrey Mathur, et al.
Pilot and Feasibility Studies|March 31, 2017
Aquatic therapy for boys with Duchenne muscular dystrophy (DMD): an external pilot randomised controlled trialDaniel Hind, James Parkin, Victoria Whitworth, et al.
Health Technology Assessment (Winchester, England)|June 20, 2017
Aquatic therapy for children with Duchenne muscular dystrophy: a pilot feasibility randomised controlled trial and mixed-methods process evaluationDaniel Hind, James Parkin, Victoria Whitworth, 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.
Pageof 4