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Lancet (London, England)
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June 11, 2019
Genotype-phenotype association in patients with SCN4A mutation - Authors' reply
Emma Matthews, Roope Männikkö, Elijah Behr, et al.
Neurologic Clinics
|
July 25, 2020
Skeletal Muscle Channelopathies
Vinojini Vivekanandam, Pinki Munot, Michael G Hanna, et al.
Expert Review of Molecular Diagnostics
|
July 14, 2020
Improving genetic diagnostics of skeletal muscle channelopathies
Vinojini Vivekanandam, Roope Männikkö, Emma Matthews, et al.
The Lancet. Child & Adolescent Health
|
March 7, 2020
Muscle and brain sodium channelopathies: genetic causes, clinical phenotypes, and management approaches
Emma Matthews, Simona Balestrini, Sanjay M Sisodiya, et al.
The Lancet. Child & Adolescent Health
|
May 7, 2022
Accelerating the genetic diagnosis of neurological disorders presenting with episodic apnoea in infancy
Bryony Silksmith, Pinki Munot, Luke Starling, et al.
The Cochrane Database of Systematic Reviews
|
May 6, 2016
Corticosteroids for the treatment of Duchenne muscular dystrophy
Emma Matthews, Ruth Brassington, Thierry Kuntzer, et al.
Archives of Neurology
|
January 12, 2011
Stridor as a neonatal presentation of skeletal muscle sodium channelopathy
Emma Matthews, Adnan Y Manzur, Richa Sud, et al.
Zeitschrift Fur Evidenz, Fortbildung Und Qualitat Im Gesundheitswesen
|
June 23, 2023
Insights into Advance Care Planning in Africa
Dianah Basirika, Anne Merriman, Nelson Gumoyesige, et al.
Journal of Human Genetics
|
February 19, 2024
Leigh syndrome with developmental regression and ataxia due to a novel splicing variant in the PMPCB gene
Emma Matthews, Ella F Whittle, Faraan Khan, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
May 18, 2018
Acetazolamide can improve symptoms and signs in ion channel-related congenital myopathy
Emma Matthews, Louise Hartley, Richa Sud, et al.
Page
of 8
Search research articles
Search
Showing results (11-20 of 71) with videos related to
Sort By:
Page
of 8
Lancet (London, England)
|
June 11, 2019
Genotype-phenotype association in patients with SCN4A mutation - Authors' reply
Emma Matthews, Roope Männikkö, Elijah Behr, et al.
Neurologic Clinics
|
July 25, 2020
Skeletal Muscle Channelopathies
Vinojini Vivekanandam, Pinki Munot, Michael G Hanna, et al.
Expert Review of Molecular Diagnostics
|
July 14, 2020
Improving genetic diagnostics of skeletal muscle channelopathies
Vinojini Vivekanandam, Roope Männikkö, Emma Matthews, et al.
The Lancet. Child & Adolescent Health
|
March 7, 2020
Muscle and brain sodium channelopathies: genetic causes, clinical phenotypes, and management approaches
Emma Matthews, Simona Balestrini, Sanjay M Sisodiya, et al.
The Lancet. Child & Adolescent Health
|
May 7, 2022
Accelerating the genetic diagnosis of neurological disorders presenting with episodic apnoea in infancy
Bryony Silksmith, Pinki Munot, Luke Starling, et al.
The Cochrane Database of Systematic Reviews
|
May 6, 2016
Corticosteroids for the treatment of Duchenne muscular dystrophy
Emma Matthews, Ruth Brassington, Thierry Kuntzer, et al.
Archives of Neurology
|
January 12, 2011
Stridor as a neonatal presentation of skeletal muscle sodium channelopathy
Emma Matthews, Adnan Y Manzur, Richa Sud, et al.
Zeitschrift Fur Evidenz, Fortbildung Und Qualitat Im Gesundheitswesen
|
June 23, 2023
Insights into Advance Care Planning in Africa
Dianah Basirika, Anne Merriman, Nelson Gumoyesige, et al.
Journal of Human Genetics
|
February 19, 2024
Leigh syndrome with developmental regression and ataxia due to a novel splicing variant in the PMPCB gene
Emma Matthews, Ella F Whittle, Faraan Khan, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
May 18, 2018
Acetazolamide can improve symptoms and signs in ion channel-related congenital myopathy
Emma Matthews, Louise Hartley, Richa Sud, et al.
Page
of 8