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Emma Matthews

Showing results (31-40 of 71) with videos related to

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Muscle & Nerve|November 24, 2021
The long exercise test as a functional marker of periodic paralysisAna Ribeiro, Karen J Suetterlin, Iwona Skorupinska, et al.
Muscle & Nerve|July 29, 2023
Muscle MRI in periodic paralysis shows myopathy is common and correlates with intramuscular fat accumulationVinojini Vivekanandam, Karen Suetterlin, Emma Matthews, et al.
Epilepsia Open|August 24, 2019
Possible role of <i>SCN4A</i> skeletal muscle mutation in apnea during seizureDilşad Türkdoğan, Emma Matthews, Sunay Usluer, et al.
Annals of Neurology|March 10, 2011
Refined exercise testing can aid DNA-based diagnosis in muscle channelopathiesS Veronica Tan, Emma Matthews, Melissa Barber, et al.
Muscle & Nerve|June 24, 2011
Sodium and chloride channelopathies with myositis: coincidence or connection?Emma Matthews, James A L Miller, Malcolm R MacLeod, et al.
Pediatric Blood & Cancer|July 16, 2024
CD3<sup>+</sup>TCRαβ/CD19<sup>+</sup>-depleted stem cell boost and CD45RO<sup>+</sup> memory T-cell add-back as a successful salvage treatment for poor graft function unresponsive to eltrombopag, following a second allogenic HSCTSubramaniam Ramanathan, Wing Roberts, Zohreh Nademi, et al.
Journal of Neuromuscular Diseases|October 19, 2020
Andersen-Tawil Syndrome Presenting with Complete Heart BlockKaren Suetterlin, Roope Männikkö, Enrico Flossmann, et al.
Scientific Reports|June 28, 2018
Hypokalaemic periodic paralysis and myotonia in a patient with homozygous mutation p.R1451L in Na<sub>V</sub>1.4Sushan Luo, Marisol Sampedro Castañeda, Emma Matthews, et al.
Brain : a Journal of Neurology|January 17, 2022
Gene variant effects across sodium channelopathies predict function and guide precision therapyAndreas Brunklaus, Tony Feng, Tobias Brünger, et al.
Circulation. Genomic and Precision Medicine|March 14, 2020
Triadin Knockout Syndrome Is Absent in a Multi-Center Molecular Autopsy Cohort of Sudden Infant Death Syndrome and Sudden Unexplained Death in the Young and Is Extremely Rare in the General PopulationDaniel J Clemens, Belinda Gray, Richard D Bagnall, et al.
Pageof 8

Showing results (31-40 of 71) with videos related to

Sort By:
Pageof 8
Muscle & Nerve|November 24, 2021
The long exercise test as a functional marker of periodic paralysisAna Ribeiro, Karen J Suetterlin, Iwona Skorupinska, et al.
Muscle & Nerve|July 29, 2023
Muscle MRI in periodic paralysis shows myopathy is common and correlates with intramuscular fat accumulationVinojini Vivekanandam, Karen Suetterlin, Emma Matthews, et al.
Epilepsia Open|August 24, 2019
Possible role of <i>SCN4A</i> skeletal muscle mutation in apnea during seizureDilşad Türkdoğan, Emma Matthews, Sunay Usluer, et al.
Annals of Neurology|March 10, 2011
Refined exercise testing can aid DNA-based diagnosis in muscle channelopathiesS Veronica Tan, Emma Matthews, Melissa Barber, et al.
Muscle & Nerve|June 24, 2011
Sodium and chloride channelopathies with myositis: coincidence or connection?Emma Matthews, James A L Miller, Malcolm R MacLeod, et al.
Pediatric Blood & Cancer|July 16, 2024
CD3<sup>+</sup>TCRαβ/CD19<sup>+</sup>-depleted stem cell boost and CD45RO<sup>+</sup> memory T-cell add-back as a successful salvage treatment for poor graft function unresponsive to eltrombopag, following a second allogenic HSCTSubramaniam Ramanathan, Wing Roberts, Zohreh Nademi, et al.
Journal of Neuromuscular Diseases|October 19, 2020
Andersen-Tawil Syndrome Presenting with Complete Heart BlockKaren Suetterlin, Roope Männikkö, Enrico Flossmann, et al.
Scientific Reports|June 28, 2018
Hypokalaemic periodic paralysis and myotonia in a patient with homozygous mutation p.R1451L in Na<sub>V</sub>1.4Sushan Luo, Marisol Sampedro Castañeda, Emma Matthews, et al.
Brain : a Journal of Neurology|January 17, 2022
Gene variant effects across sodium channelopathies predict function and guide precision therapyAndreas Brunklaus, Tony Feng, Tobias Brünger, et al.
Circulation. Genomic and Precision Medicine|March 14, 2020
Triadin Knockout Syndrome Is Absent in a Multi-Center Molecular Autopsy Cohort of Sudden Infant Death Syndrome and Sudden Unexplained Death in the Young and Is Extremely Rare in the General PopulationDaniel J Clemens, Belinda Gray, Richard D Bagnall, et al.
Pageof 8