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Brain : a Journal of Neurology
|
November 14, 2018
A novel ATP1A2 mutation in a patient with hypokalaemic periodic paralysis and CNS symptoms
Marisol Sampedro Castañeda, Edmar Zanoteli, Renata S Scalco, et al.
Brain : a Journal of Neurology
|
December 17, 2021
Andersen-Tawil syndrome: deep phenotyping reveals significant cardiac and neuromuscular morbidity
Vinojini Vivekanandam, Roope Männikkö, Iwona Skorupinska, et al.
Brain : a Journal of Neurology
|
June 18, 2013
Non-dystrophic myotonia: prospective study of objective and patient reported outcomes
Jaya R Trivedi, Brian Bundy, Jeffrey Statland, et al.
JAMA
|
October 4, 2012
Mexiletine for symptoms and signs of myotonia in nondystrophic myotonia: a randomized controlled trial
Jeffrey M Statland, Brian N Bundy, Yunxia Wang, et al.
Muscle & Nerve
|
April 10, 2020
Guidelines on clinical presentation and management of nondystrophic myotonias
Bas C Stunnenberg, Samantha LoRusso, W David Arnold, et al.
JAMA
|
December 12, 2018
Effect of Mexiletine on Muscle Stiffness in Patients With Nondystrophic Myotonia Evaluated Using Aggregated N-of-1 Trials
Bas C Stunnenberg, Joost Raaphorst, Hans M Groenewoud, et al.
Neurology
|
January 5, 2018
Atypical periodic paralysis and myalgia: A novel <i>RYR1</i> phenotype
Emma Matthews, Christoph Neuwirth, Fatima Jaffer, et al.
Neuromuscular Disorders : NMD
|
January 19, 2010
Multi-minicore disease and atypical periodic paralysis associated with novel mutations in the skeletal muscle ryanodine receptor (RYR1) gene
Haiyan Zhou, Suzanne Lillis, Ryan E Loy, et al.
Human Mutation
|
June 24, 2018
The analysis of myotonia congenita mutations discloses functional clusters of amino acids within the CBS2 domain and the C-terminal peptide of the ClC-1 channel
Concetta Altamura, Sabrina Lucchiari, Dalila Sahbani, et al.
Muscle & Nerve
|
September 19, 2012
A quantitative measure of handgrip myotonia in non-dystrophic myotonia
Jeffrey M Statland, Brian N Bundy, Yunxia Wang, et al.
Page
of 8
Search research articles
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Showing results (51-60 of 71) with videos related to
Sort By:
Page
of 8
Brain : a Journal of Neurology
|
November 14, 2018
A novel ATP1A2 mutation in a patient with hypokalaemic periodic paralysis and CNS symptoms
Marisol Sampedro Castañeda, Edmar Zanoteli, Renata S Scalco, et al.
Brain : a Journal of Neurology
|
December 17, 2021
Andersen-Tawil syndrome: deep phenotyping reveals significant cardiac and neuromuscular morbidity
Vinojini Vivekanandam, Roope Männikkö, Iwona Skorupinska, et al.
Brain : a Journal of Neurology
|
June 18, 2013
Non-dystrophic myotonia: prospective study of objective and patient reported outcomes
Jaya R Trivedi, Brian Bundy, Jeffrey Statland, et al.
JAMA
|
October 4, 2012
Mexiletine for symptoms and signs of myotonia in nondystrophic myotonia: a randomized controlled trial
Jeffrey M Statland, Brian N Bundy, Yunxia Wang, et al.
Muscle & Nerve
|
April 10, 2020
Guidelines on clinical presentation and management of nondystrophic myotonias
Bas C Stunnenberg, Samantha LoRusso, W David Arnold, et al.
JAMA
|
December 12, 2018
Effect of Mexiletine on Muscle Stiffness in Patients With Nondystrophic Myotonia Evaluated Using Aggregated N-of-1 Trials
Bas C Stunnenberg, Joost Raaphorst, Hans M Groenewoud, et al.
Neurology
|
January 5, 2018
Atypical periodic paralysis and myalgia: A novel <i>RYR1</i> phenotype
Emma Matthews, Christoph Neuwirth, Fatima Jaffer, et al.
Neuromuscular Disorders : NMD
|
January 19, 2010
Multi-minicore disease and atypical periodic paralysis associated with novel mutations in the skeletal muscle ryanodine receptor (RYR1) gene
Haiyan Zhou, Suzanne Lillis, Ryan E Loy, et al.
Human Mutation
|
June 24, 2018
The analysis of myotonia congenita mutations discloses functional clusters of amino acids within the CBS2 domain and the C-terminal peptide of the ClC-1 channel
Concetta Altamura, Sabrina Lucchiari, Dalila Sahbani, et al.
Muscle & Nerve
|
September 19, 2012
A quantitative measure of handgrip myotonia in non-dystrophic myotonia
Jeffrey M Statland, Brian N Bundy, Yunxia Wang, et al.
Page
of 8