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Katherine D Mathews

Showing results (11-20 of 125) with videos related to

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American Family Physician|January 16, 2015
Recognition and management of motor delay and muscle weakness in childrenJoseph G Lurio, Holly L Peay, Katherine D Mathews
The Annals of Otology, Rhinology, and Laryngology|July 26, 2014
The boy who lost his smile: facioscapulohumeral dystrophy in the head and neckJonathan C Kopelovich, Scott Owen, Katherine D Mathews, et al.
Neurology|January 14, 2021
CLIA Laboratory Testing for Facioscapulohumeral Dystrophy: A Retrospective AnalysisAutumn Rieken, Aaron D Bossler, Katherine D Mathews, et al.
Advances in Neurology|March 23, 2002
Limb-girdle muscular dystrophiesFederica Piccolo, Steven A Moore, Katherine D Mathews, et al.
Muscle & Nerve|September 25, 2004
The sarcolemma in the Large(myd) mousePatrick W Reed, Katherine D Mathews, Kathleen A Mills, et al.
Journal of Neuromuscular Diseases|April 5, 2021
Vitamin D Level Stability in Dystrophinopathy Patients on Vitamin D SupplementationNaomi Vather-Wu, Matthew D Krasowski, Katherine D Mathews, et al.
Journal of the Peripheral Nervous System : JPNS|April 3, 2012
Infantile onset CMT2D/dSMA V in monozygotic twins due to a mutation in the anticodon-binding domain of GARSJamie M Eskuri, Christine M Stanley, Steven A Moore, et al.
Journal of Child Neurology|May 22, 2018
Descriptive Phenotype of Obsessive Compulsive Symptoms in Males With Duchenne Muscular DystrophyAngela J Lee, Edward T Buckingham, Aaron J Kauer, et al.
Neurology|September 18, 2013
Clinical and genetic features of hearing loss in facioscapulohumeral muscular dystrophyKatie L Lutz, Lenore Holte, Stephanie A Kliethermes, et al.
Journal of Clinical Neuromuscular Disease|May 23, 2023
DMD Gene and Dystrophinopathy Phenotypes Associated With Mutations: A Systematic Review for CliniciansJennifer G Andrews, Maureen Kelly Galindo, Shiny Thomas, et al.
Pageof 13

Showing results (11-20 of 125) with videos related to

Sort By:
Pageof 13
American Family Physician|January 16, 2015
Recognition and management of motor delay and muscle weakness in childrenJoseph G Lurio, Holly L Peay, Katherine D Mathews
The Annals of Otology, Rhinology, and Laryngology|July 26, 2014
The boy who lost his smile: facioscapulohumeral dystrophy in the head and neckJonathan C Kopelovich, Scott Owen, Katherine D Mathews, et al.
Neurology|January 14, 2021
CLIA Laboratory Testing for Facioscapulohumeral Dystrophy: A Retrospective AnalysisAutumn Rieken, Aaron D Bossler, Katherine D Mathews, et al.
Advances in Neurology|March 23, 2002
Limb-girdle muscular dystrophiesFederica Piccolo, Steven A Moore, Katherine D Mathews, et al.
Muscle & Nerve|September 25, 2004
The sarcolemma in the Large(myd) mousePatrick W Reed, Katherine D Mathews, Kathleen A Mills, et al.
Journal of Neuromuscular Diseases|April 5, 2021
Vitamin D Level Stability in Dystrophinopathy Patients on Vitamin D SupplementationNaomi Vather-Wu, Matthew D Krasowski, Katherine D Mathews, et al.
Journal of the Peripheral Nervous System : JPNS|April 3, 2012
Infantile onset CMT2D/dSMA V in monozygotic twins due to a mutation in the anticodon-binding domain of GARSJamie M Eskuri, Christine M Stanley, Steven A Moore, et al.
Journal of Child Neurology|May 22, 2018
Descriptive Phenotype of Obsessive Compulsive Symptoms in Males With Duchenne Muscular DystrophyAngela J Lee, Edward T Buckingham, Aaron J Kauer, et al.
Neurology|September 18, 2013
Clinical and genetic features of hearing loss in facioscapulohumeral muscular dystrophyKatie L Lutz, Lenore Holte, Stephanie A Kliethermes, et al.
Journal of Clinical Neuromuscular Disease|May 23, 2023
DMD Gene and Dystrophinopathy Phenotypes Associated With Mutations: A Systematic Review for CliniciansJennifer G Andrews, Maureen Kelly Galindo, Shiny Thomas, et al.
Pageof 13