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Neurology. Clinical Practice
|
February 18, 2026
Assessing the Relationship of Quality of Life With Functional Status in a Large Cohort of Adult Patients With Neuromuscular Disorders
Karen S W Wong, Anando Sen, Jassi Michell-Sodhi, et al.
Brain : a Journal of Neurology
|
May 8, 2007
Molecular mechanisms and phenotypic variation in RYR1-related congenital myopathies
Haiyan Zhou, Heinz Jungbluth, Caroline A Sewry, et al.
Brain : a Journal of Neurology
|
December 28, 2010
A founder mutation in Anoctamin 5 is a major cause of limb-girdle muscular dystrophy
Debbie Hicks, Anna Sarkozy, Nuria Muelas, et al.
The Lancet. Neurology
|
September 12, 2014
Safety and efficacy of drisapersen for the treatment of Duchenne muscular dystrophy (DEMAND II): an exploratory, randomised, placebo-controlled phase 2 study
Thomas Voit, Haluk Topaloglu, Volker Straub, et al.
Neurology
|
October 31, 2014
Dystrophin quantification: Biological and translational research implications
Karen Anthony, Virginia Arechavala-Gomeza, Laura E Taylor, et al.
Journal of Neuromuscular Diseases
|
September 27, 2021
Effects of Chronic, Maximal Phosphorodiamidate Morpholino Oligomer (PMO) Dosing on Muscle Function and Dystrophin Restoration in a Mouse Model of Duchenne Muscular Dystrophy
Margaret E Benny Klimek, Maria Candida Vila, Katie Edwards, et al.
Neurology
|
February 1, 2023
<i>DMD</i> Genotypes and Motor Function in Duchenne Muscular Dystrophy: A Multi-institution Meta-analysis With Implications for Clinical Trials
Francesco Muntoni, James Signorovitch, Gautam Sajeev, et al.
Neuromuscular Disorders : NMD
|
March 9, 2010
Genotype-phenotype correlation in a large population of muscular dystrophy patients with LAMA2 mutations
Fatemeh Geranmayeh, Emma Clement, Lucy H Feng, et al.
Brain : a Journal of Neurology
|
November 22, 2011
Dystrophin quantification and clinical correlations in Becker muscular dystrophy: implications for clinical trials
Karen Anthony, Sebahattin Cirak, Silvia Torelli, et al.
Plos One
|
April 26, 2023
Determining minimal clinically important differences in the North Star Ambulatory Assessment (NSAA) for patients with Duchenne muscular dystrophy
Vandana Ayyar Gupta, Jacqueline M Pitchforth, Joana Domingos, et al.
Page
of 38
Search research articles
Search
Showing results (221-230 of 374) with videos related to
Sort By:
Page
of 38
Neurology. Clinical Practice
|
February 18, 2026
Assessing the Relationship of Quality of Life With Functional Status in a Large Cohort of Adult Patients With Neuromuscular Disorders
Karen S W Wong, Anando Sen, Jassi Michell-Sodhi, et al.
Brain : a Journal of Neurology
|
May 8, 2007
Molecular mechanisms and phenotypic variation in RYR1-related congenital myopathies
Haiyan Zhou, Heinz Jungbluth, Caroline A Sewry, et al.
Brain : a Journal of Neurology
|
December 28, 2010
A founder mutation in Anoctamin 5 is a major cause of limb-girdle muscular dystrophy
Debbie Hicks, Anna Sarkozy, Nuria Muelas, et al.
The Lancet. Neurology
|
September 12, 2014
Safety and efficacy of drisapersen for the treatment of Duchenne muscular dystrophy (DEMAND II): an exploratory, randomised, placebo-controlled phase 2 study
Thomas Voit, Haluk Topaloglu, Volker Straub, et al.
Neurology
|
October 31, 2014
Dystrophin quantification: Biological and translational research implications
Karen Anthony, Virginia Arechavala-Gomeza, Laura E Taylor, et al.
Journal of Neuromuscular Diseases
|
September 27, 2021
Effects of Chronic, Maximal Phosphorodiamidate Morpholino Oligomer (PMO) Dosing on Muscle Function and Dystrophin Restoration in a Mouse Model of Duchenne Muscular Dystrophy
Margaret E Benny Klimek, Maria Candida Vila, Katie Edwards, et al.
Neurology
|
February 1, 2023
<i>DMD</i> Genotypes and Motor Function in Duchenne Muscular Dystrophy: A Multi-institution Meta-analysis With Implications for Clinical Trials
Francesco Muntoni, James Signorovitch, Gautam Sajeev, et al.
Neuromuscular Disorders : NMD
|
March 9, 2010
Genotype-phenotype correlation in a large population of muscular dystrophy patients with LAMA2 mutations
Fatemeh Geranmayeh, Emma Clement, Lucy H Feng, et al.
Brain : a Journal of Neurology
|
November 22, 2011
Dystrophin quantification and clinical correlations in Becker muscular dystrophy: implications for clinical trials
Karen Anthony, Sebahattin Cirak, Silvia Torelli, et al.
Plos One
|
April 26, 2023
Determining minimal clinically important differences in the North Star Ambulatory Assessment (NSAA) for patients with Duchenne muscular dystrophy
Vandana Ayyar Gupta, Jacqueline M Pitchforth, Joana Domingos, et al.
Page
of 38