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Kate Bushby

Showing results (41-50 of 151) with videos related to

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Neuromuscular Disorders : NMD|November 11, 2008
Sarcoglycanopathies: can muscle immunoanalysis predict the genotype?Lars Klinge, Gabriele Dekomien, Ahmed Aboumousa, et al.
Physical Medicine and Rehabilitation Clinics of North America|November 10, 2012
Novel approaches to corticosteroid treatment in Duchenne muscular dystrophyEric P Hoffman, Erica Reeves, Jesse Damsker, et al.
The Journal of Biological Chemistry|December 22, 2007
Caveolin regulates endocytosis of the muscle repair protein, dysferlinDelia J Hernández-Deviez, Mark T Howes, Steven H Laval, et al.
Orphanet Journal of Rare Diseases|October 24, 2013
The TREAT-NMD care and trial site registry: an online registry to facilitate clinical research for neuromuscular diseasesSunil Rodger, Hanns Lochmüller, Adrian Tassoni, et al.
JAMA Neurology|March 12, 2019
Fractures and Linear Growth in a Nationwide Cohort of Boys With Duchenne Muscular Dystrophy With and Without Glucocorticoid Treatment: Results From the UK NorthStar DatabaseShuko Joseph, Cunyi Wang, Kate Bushby, et al.
Journal of Neuromuscular Diseases|February 13, 2016
Muscle-Derived Proteins as Serum Biomarkers for Monitoring Disease Progression in Three Forms of Muscular DystrophyPeter M Burch, Oksana Pogoryelova, Richard Goldstein, et al.
Plos Currents|June 22, 2013
Undiagnosed genetic muscle disease in the north of England: an in depth phenotype analysisElizabeth Harris, Steve Laval, Judith Hudson, et al.
Human Molecular Genetics|September 20, 2011
Abnormal vascular development in zebrafish models for fukutin and FKRP deficiencyAlasdair J Wood, Juliane S Müller, Catherine D Jepson, et al.
European Journal of Human Genetics : EJHG|March 5, 2009
Does delta-sarcoglycan-associated autosomal-dominant cardiomyopathy exist?Ralf Bauer, Judith Hudson, Harald D Müller, et al.
Annals of Neurology|February 29, 2008
Dysferlin-deficient muscular dystrophy features amyloidosisSimone Spuler, Miriam Carl, Joanna Zabojszcza, et al.
Pageof 16

Showing results (41-50 of 151) with videos related to

Sort By:
Pageof 16
Neuromuscular Disorders : NMD|November 11, 2008
Sarcoglycanopathies: can muscle immunoanalysis predict the genotype?Lars Klinge, Gabriele Dekomien, Ahmed Aboumousa, et al.
Physical Medicine and Rehabilitation Clinics of North America|November 10, 2012
Novel approaches to corticosteroid treatment in Duchenne muscular dystrophyEric P Hoffman, Erica Reeves, Jesse Damsker, et al.
The Journal of Biological Chemistry|December 22, 2007
Caveolin regulates endocytosis of the muscle repair protein, dysferlinDelia J Hernández-Deviez, Mark T Howes, Steven H Laval, et al.
Orphanet Journal of Rare Diseases|October 24, 2013
The TREAT-NMD care and trial site registry: an online registry to facilitate clinical research for neuromuscular diseasesSunil Rodger, Hanns Lochmüller, Adrian Tassoni, et al.
JAMA Neurology|March 12, 2019
Fractures and Linear Growth in a Nationwide Cohort of Boys With Duchenne Muscular Dystrophy With and Without Glucocorticoid Treatment: Results From the UK NorthStar DatabaseShuko Joseph, Cunyi Wang, Kate Bushby, et al.
Journal of Neuromuscular Diseases|February 13, 2016
Muscle-Derived Proteins as Serum Biomarkers for Monitoring Disease Progression in Three Forms of Muscular DystrophyPeter M Burch, Oksana Pogoryelova, Richard Goldstein, et al.
Plos Currents|June 22, 2013
Undiagnosed genetic muscle disease in the north of England: an in depth phenotype analysisElizabeth Harris, Steve Laval, Judith Hudson, et al.
Human Molecular Genetics|September 20, 2011
Abnormal vascular development in zebrafish models for fukutin and FKRP deficiencyAlasdair J Wood, Juliane S Müller, Catherine D Jepson, et al.
European Journal of Human Genetics : EJHG|March 5, 2009
Does delta-sarcoglycan-associated autosomal-dominant cardiomyopathy exist?Ralf Bauer, Judith Hudson, Harald D Müller, et al.
Annals of Neurology|February 29, 2008
Dysferlin-deficient muscular dystrophy features amyloidosisSimone Spuler, Miriam Carl, Joanna Zabojszcza, et al.
Pageof 16