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Neurology
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January 21, 2021
Population-Based Prevalence of Myotonic Dystrophy Type 1 Using Genetic Analysis of Statewide Blood Screening Program
Nicholas E Johnson, Russell J Butterfield, Katie Mayne, et al.
Muscle & Nerve
|
January 7, 2022
Evaluation of effects of continued corticosteroid treatment on cardiac and pulmonary function in non-ambulatory males with Duchenne muscular dystrophy from MD STARnet
Russell J Butterfield, Sergey Kirkov, Kristin M Conway, et al.
Children (Basel, Switzerland)
|
October 23, 2021
Characteristics of Clinical Trial Participants with Duchenne Muscular Dystrophy: Data from the Muscular Dystrophy Surveillance, Tracking, and Research Network (MD STAR<i>net</i>)
Katherine D Mathews, Kristin M Conway, Amber M Gedlinske, et al.
Molecular Genetics & Genomic Medicine
|
February 24, 2021
High throughput screening for expanded CTG repeats in myotonic dystrophy type 1 using melt curve analysis
Russell J Butterfield, Carina Imburgia, Katie Mayne, et al.
The Lancet. Respiratory Medicine
|
April 1, 2022
Cardiorespiratory management of Duchenne muscular dystrophy: emerging therapies, neuromuscular genetics, and new clinical challenges
David J Birnkrant, Luca Bello, Russell J Butterfield, et al.
Journal of Immunology (Baltimore, Md. : 1950)
|
July 23, 2002
Interacting quantitative trait loci control loss of peripheral tolerance and susceptibility to autoimmune ovarian dysgenesis after day 3 thymectomy in mice
Randall J Roper, Runlin Z Ma, Julia E Biggins, et al.
Neurology
|
February 15, 2024
Neurobehavioral Phenotype of Children With Congenital Myotonic Dystrophy
Namita Patel, Kiera N Berggren, Man Hung, et al.
Muscle & Nerve
|
June 15, 2018
Orofacial strength, dysarthria, and dysphagia in congenital myotonic dystrophy
Kiera N Berggren, Man Hung, Melissa M Dixon, et al.
Scientific Reports
|
November 6, 2022
Dual-energy X-ray absorptiometry measures of lean body mass as a biomarker for progression in boys with Duchenne muscular dystrophy
Sarah P Sherlock, Jeffrey Palmer, Kathryn R Wagner, et al.
Neurology
|
May 14, 2025
Delandistrogene Moxeparvovec Gene Therapy in Individuals With Duchenne Muscular Dystrophy: Evidence in Focus: Report of the AAN Guidelines Subcommittee
Maryam Oskoui, Tracie Anne Caller, Julie A Parsons, et al.
Page
of 8
Search research articles
Search
Showing results (21-30 of 73) with videos related to
Sort By:
Page
of 8
Neurology
|
January 21, 2021
Population-Based Prevalence of Myotonic Dystrophy Type 1 Using Genetic Analysis of Statewide Blood Screening Program
Nicholas E Johnson, Russell J Butterfield, Katie Mayne, et al.
Muscle & Nerve
|
January 7, 2022
Evaluation of effects of continued corticosteroid treatment on cardiac and pulmonary function in non-ambulatory males with Duchenne muscular dystrophy from MD STARnet
Russell J Butterfield, Sergey Kirkov, Kristin M Conway, et al.
Children (Basel, Switzerland)
|
October 23, 2021
Characteristics of Clinical Trial Participants with Duchenne Muscular Dystrophy: Data from the Muscular Dystrophy Surveillance, Tracking, and Research Network (MD STAR<i>net</i>)
Katherine D Mathews, Kristin M Conway, Amber M Gedlinske, et al.
Molecular Genetics & Genomic Medicine
|
February 24, 2021
High throughput screening for expanded CTG repeats in myotonic dystrophy type 1 using melt curve analysis
Russell J Butterfield, Carina Imburgia, Katie Mayne, et al.
The Lancet. Respiratory Medicine
|
April 1, 2022
Cardiorespiratory management of Duchenne muscular dystrophy: emerging therapies, neuromuscular genetics, and new clinical challenges
David J Birnkrant, Luca Bello, Russell J Butterfield, et al.
Journal of Immunology (Baltimore, Md. : 1950)
|
July 23, 2002
Interacting quantitative trait loci control loss of peripheral tolerance and susceptibility to autoimmune ovarian dysgenesis after day 3 thymectomy in mice
Randall J Roper, Runlin Z Ma, Julia E Biggins, et al.
Neurology
|
February 15, 2024
Neurobehavioral Phenotype of Children With Congenital Myotonic Dystrophy
Namita Patel, Kiera N Berggren, Man Hung, et al.
Muscle & Nerve
|
June 15, 2018
Orofacial strength, dysarthria, and dysphagia in congenital myotonic dystrophy
Kiera N Berggren, Man Hung, Melissa M Dixon, et al.
Scientific Reports
|
November 6, 2022
Dual-energy X-ray absorptiometry measures of lean body mass as a biomarker for progression in boys with Duchenne muscular dystrophy
Sarah P Sherlock, Jeffrey Palmer, Kathryn R Wagner, et al.
Neurology
|
May 14, 2025
Delandistrogene Moxeparvovec Gene Therapy in Individuals With Duchenne Muscular Dystrophy: Evidence in Focus: Report of the AAN Guidelines Subcommittee
Maryam Oskoui, Tracie Anne Caller, Julie A Parsons, et al.
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of 8