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Katherine D Mathews

Showing results (71-80 of 125) with videos related to

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Orphanet Journal of Rare Diseases|August 8, 2013
Genotype-phenotype correlations in recessive RYR1-related myopathiesKimberly Amburgey, Angela Bailey, Jean H Hwang, et al.
Journal of Child Neurology|December 17, 2008
Mutation analysis in a population-based cohort of boys with Duchenne or Becker muscular dystrophyChristopher Cunniff, Jennifer Andrews, F John Meaney, et al.
Journal of the Neurological Sciences|November 9, 2007
Antioxidant use in Friedreich ataxiaLauren Myers, Jennifer M Farmer, Robert B Wilson, et al.
The Journal of Pediatrics|April 28, 2009
Delayed diagnosis in duchenne muscular dystrophy: data from the Muscular Dystrophy Surveillance, Tracking, and Research Network (MD STARnet)Emma Ciafaloni, Deborah J Fox, Shree Pandya, et al.
Nature|July 26, 2002
Post-translational disruption of dystroglycan-ligand interactions in congenital muscular dystrophiesDaniel E Michele, Rita Barresi, Motoi Kanagawa, et al.
Journal of Child Neurology|December 14, 2011
Use of complementary and alternative medicine by males with Duchenne or Becker muscular dystrophySarah K Nabukera, Paul A Romitti, Kimberly A Campbell, et al.
Journal of Child Neurology|March 9, 2010
Use of corticosteroids in a population-based cohort of boys with duchenne and becker muscular dystrophyDennis J Matthews, Katherine A James, Lisa A Miller, et al.
The American Journal of Cardiology|November 15, 2011
Analysis of echocardiograms in a large heterogeneous cohort of patients with friedreich ataxiaSean R Regner, Sarah J Lagedrost, Ted Plappert, et al.
Muscle & Nerve|April 25, 2020
Spinal muscular atrophy care in the COVID-19 pandemic eraAravindhan Veerapandiyan, Anne M Connolly, Richard S Finkel, et al.
Neurology. Genetics|February 12, 2020
Psychometric properties of the Friedreich Ataxia Rating ScaleChristian Rummey, Louise A Corben, Martin B Delatycki, et al.
Pageof 13

Showing results (71-80 of 125) with videos related to

Sort By:
Pageof 13
Orphanet Journal of Rare Diseases|August 8, 2013
Genotype-phenotype correlations in recessive RYR1-related myopathiesKimberly Amburgey, Angela Bailey, Jean H Hwang, et al.
Journal of Child Neurology|December 17, 2008
Mutation analysis in a population-based cohort of boys with Duchenne or Becker muscular dystrophyChristopher Cunniff, Jennifer Andrews, F John Meaney, et al.
Journal of the Neurological Sciences|November 9, 2007
Antioxidant use in Friedreich ataxiaLauren Myers, Jennifer M Farmer, Robert B Wilson, et al.
The Journal of Pediatrics|April 28, 2009
Delayed diagnosis in duchenne muscular dystrophy: data from the Muscular Dystrophy Surveillance, Tracking, and Research Network (MD STARnet)Emma Ciafaloni, Deborah J Fox, Shree Pandya, et al.
Nature|July 26, 2002
Post-translational disruption of dystroglycan-ligand interactions in congenital muscular dystrophiesDaniel E Michele, Rita Barresi, Motoi Kanagawa, et al.
Journal of Child Neurology|December 14, 2011
Use of complementary and alternative medicine by males with Duchenne or Becker muscular dystrophySarah K Nabukera, Paul A Romitti, Kimberly A Campbell, et al.
Journal of Child Neurology|March 9, 2010
Use of corticosteroids in a population-based cohort of boys with duchenne and becker muscular dystrophyDennis J Matthews, Katherine A James, Lisa A Miller, et al.
The American Journal of Cardiology|November 15, 2011
Analysis of echocardiograms in a large heterogeneous cohort of patients with friedreich ataxiaSean R Regner, Sarah J Lagedrost, Ted Plappert, et al.
Muscle & Nerve|April 25, 2020
Spinal muscular atrophy care in the COVID-19 pandemic eraAravindhan Veerapandiyan, Anne M Connolly, Richard S Finkel, et al.
Neurology. Genetics|February 12, 2020
Psychometric properties of the Friedreich Ataxia Rating ScaleChristian Rummey, Louise A Corben, Martin B Delatycki, et al.
Pageof 13