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Katherine D Mathews

Showing results (61-70 of 125) with videos related to

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Neurology|January 15, 2017
Comparison of brain MRI findings with language and motor function in the dystroglycanopathiesBrianna N Brun, Shelley R H Mockler, Katie M Laubscher, et al.
American Journal of Medical Genetics. Part A|December 15, 2012
Reproductive patterns among mothers of males diagnosed with Duchenne or Becker muscular dystrophySarah K Nabukera, Paul A Romitti, Kristin M Caspers, et al.
Journal of Neuropathology and Experimental Neurology|August 23, 2020
Cobblestone Malformation in LAMA2 Congenital Muscular Dystrophy (MDC1A)Himali Jayakody, Sanam Zarei, Huy Nguyen, et al.
Neurology. Clinical Practice|August 4, 2025
Limb-Girdle Muscular Dystrophy Scientific Workshop: A Multistakeholder Discussion Focused on Charting the Path Forward for Drug DevelopmentMatthew P Wicklund, Lindsay N Alfano, Nicholas E Johnson, et al.
Human Mutation|August 28, 2015
GMPPB-Associated Dystroglycanopathy: Emerging Common Variants with Phenotype CorrelationBraden S Jensen, Tobias Willer, Dimah N Saade, et al.
Journal of Neurology|December 3, 2022
Double blind trial of a deuterated form of linoleic acid (RT001) in Friedreich ataxiaDavid R Lynch, Katherine D Mathews, Susan Perlman, et al.
Cells|March 29, 2023
A De Novo Sequence Variant in Barrier-to-Autointegration Factor Is Associated with Dominant Motor NeuronopathyAgathe Marcelot, Felipe Rodriguez-Tirado, Philippe Cuniasse, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|January 12, 2010
Measuring the rate of progression in Friedreich ataxia: implications for clinical trial designLisa S Friedman, Jennifer M Farmer, Susan Perlman, et al.
Muscle & Nerve|September 11, 2020
Cardiomyopathy in limb girdle muscular dystrophy R9, FKRP relatedEric M Libell, Julia A Richardson, Katie L Lutz, et al.
Neuromuscular Disorders : NMD|March 4, 2014
Diagnostic approach to the congenital muscular dystrophiesCarsten G Bönnemann, Ching H Wang, Susana Quijano-Roy, et al.
Pageof 13

Showing results (61-70 of 125) with videos related to

Sort By:
Pageof 13
Neurology|January 15, 2017
Comparison of brain MRI findings with language and motor function in the dystroglycanopathiesBrianna N Brun, Shelley R H Mockler, Katie M Laubscher, et al.
American Journal of Medical Genetics. Part A|December 15, 2012
Reproductive patterns among mothers of males diagnosed with Duchenne or Becker muscular dystrophySarah K Nabukera, Paul A Romitti, Kristin M Caspers, et al.
Journal of Neuropathology and Experimental Neurology|August 23, 2020
Cobblestone Malformation in LAMA2 Congenital Muscular Dystrophy (MDC1A)Himali Jayakody, Sanam Zarei, Huy Nguyen, et al.
Neurology. Clinical Practice|August 4, 2025
Limb-Girdle Muscular Dystrophy Scientific Workshop: A Multistakeholder Discussion Focused on Charting the Path Forward for Drug DevelopmentMatthew P Wicklund, Lindsay N Alfano, Nicholas E Johnson, et al.
Human Mutation|August 28, 2015
GMPPB-Associated Dystroglycanopathy: Emerging Common Variants with Phenotype CorrelationBraden S Jensen, Tobias Willer, Dimah N Saade, et al.
Journal of Neurology|December 3, 2022
Double blind trial of a deuterated form of linoleic acid (RT001) in Friedreich ataxiaDavid R Lynch, Katherine D Mathews, Susan Perlman, et al.
Cells|March 29, 2023
A De Novo Sequence Variant in Barrier-to-Autointegration Factor Is Associated with Dominant Motor NeuronopathyAgathe Marcelot, Felipe Rodriguez-Tirado, Philippe Cuniasse, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|January 12, 2010
Measuring the rate of progression in Friedreich ataxia: implications for clinical trial designLisa S Friedman, Jennifer M Farmer, Susan Perlman, et al.
Muscle & Nerve|September 11, 2020
Cardiomyopathy in limb girdle muscular dystrophy R9, FKRP relatedEric M Libell, Julia A Richardson, Katie L Lutz, et al.
Neuromuscular Disorders : NMD|March 4, 2014
Diagnostic approach to the congenital muscular dystrophiesCarsten G Bönnemann, Ching H Wang, Susana Quijano-Roy, et al.
Pageof 13