Articles with "neuromuscular disorder" as a keyword



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Parents’ perceptions of power wheelchair prescription for children with a neuromuscular disorder: a scoping review

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Published in 2018 at "Disability and Rehabilitation"

DOI: 10.1080/09638288.2018.1474496

Abstract: Abstract Purpose: To conduct a scoping review of the published evidence on parents’ perceptions of power wheelchair prescription for children with a neuromuscular disorder and clinicians’ influence on timely wheelchair implementation. Method: Nine electronic databases… read more here.

Keywords: neuromuscular disorder; wheelchair prescription; power wheelchair; wheelchair ... See more keywords
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Causes of HyperCKemia in Children: A Retrospective Cohort Study

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Published in 2022 at "Journal of Child Neurology"

DOI: 10.1177/08830738221147808

Abstract: Background and Objectives: Creatine kinase (CK) is a commonly used screening test for neuromuscular disorders (NMDs). However, hyperCKemia can result from several pathologic and physiologic causes. We analyzed neuromuscular disorders in noninfant children with hyperCKemia… read more here.

Keywords: limit normal; upper limit; neuromuscular disorders; neuromuscular disorder ... See more keywords
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Overview of Neuromuscular Disorder Molecular Diagnostic Experience for the Population of Latvia

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Published in 2022 at "Neurology: Genetics"

DOI: 10.1212/nxg.0000000000000685

Abstract: Background and Objectives Genetic testing has become an integral part of health care, allowing the confirmation of thousands of hereditary diseases, including neuromuscular disorders (NMDs). The reported average prevalence of individual inherited NMDs is 3.7–4.99… read more here.

Keywords: prevalence; population latvia; neuromuscular disorder; overview neuromuscular ... See more keywords
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Of rAAV and Men: From Genetic Neuromuscular Disorder Efficacy and Toxicity Preclinical Studies to Clinical Trials and Back

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Published in 2020 at "Journal of Personalized Medicine"

DOI: 10.3390/jpm10040258

Abstract: Neuromuscular disorders are a large group of rare pathologies characterised by skeletal muscle atrophy and weakness, with the common involvement of respiratory and/or cardiac muscles. These diseases lead to life-long motor deficiencies and specific organ… read more here.

Keywords: efficacy; clinical trials; men genetic; raav men ... See more keywords