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Journal of Neurology, Neurosurgery, and Psychiatry
|
January 7, 2026
Spectrum of dominant Charcot-Marie-Tooth disease due to <i>SLC12A6</i> variants
Christopher J Record, Tiffany Grider, Adriana P Rebelo, et al.
Clinical Neurophysiology : Official Journal of the International Federation of Clinical Neurophysiology
|
May 28, 2018
Implementing Motor Unit Number Index (MUNIX) in a large clinical trial: Real world experience from 27 centres
Christoph Neuwirth, Nathalie Braun, Kristl G Claeys, et al.
Brain : a Journal of Neurology
|
March 13, 2023
Anoctamin-5 related muscle disease: clinical and genetic findings in a large European cohort
Alexander de Bruyn, Federica Montagnese, Sonja Holm-Yildiz, et al.
Brain : a Journal of Neurology
|
January 18, 2018
Hot-spot KIF5A mutations cause familial ALS
David Brenner, Rüstem Yilmaz, Kathrin Müller, et al.
Orphanet Journal of Rare Diseases
|
February 14, 2024
EURO-NMD registry: federated FAIR infrastructure, innovative technologies and concepts of a patient-centred registry for rare neuromuscular disorders
Antonio Atalaia, Dagmar Wandrei, Nawel Lalout, et al.
Nature Communications
|
March 29, 2019
Myoglobinopathy is an adult-onset autosomal dominant myopathy with characteristic sarcoplasmic inclusions
Montse Olivé, Martin Engvall, Gianina Ravenscroft, et al.
Brain : a Journal of Neurology
|
May 23, 2006
MFN2 mutation distribution and genotype/phenotype correlation in Charcot-Marie-Tooth type 2
Kristien Verhoeven, Kristl G Claeys, Stephan Züchner, et al.
Annals of Clinical and Translational Neurology
|
December 31, 2025
Whole-Body Pattern of Muscle Degeneration and Progression in Sarcoglycanopathies
Laura Costa-Comellas, Mauro Monforte, Angel Sanchez-Montañez, et al.
The Lancet. Neurology
|
October 5, 2007
Multicentre search for genetic susceptibility loci in sporadic epilepsy syndrome and seizure types: a case-control study
Gianpiero L Cavalleri, Michael E Weale, Kevin V Shianna, et al.
Brain : a Journal of Neurology
|
May 15, 2023
The emerging spectrum of fetal acetylcholine receptor antibody-related disorders (FARAD)
Nicholas M Allen, Mark O'Rahelly, Bruno Eymard, et al.
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of 24
Search research articles
Search
Showing results (221-230 of 239) with videos related to
Sort By:
Page
of 24
Journal of Neurology, Neurosurgery, and Psychiatry
|
January 7, 2026
Spectrum of dominant Charcot-Marie-Tooth disease due to <i>SLC12A6</i> variants
Christopher J Record, Tiffany Grider, Adriana P Rebelo, et al.
Clinical Neurophysiology : Official Journal of the International Federation of Clinical Neurophysiology
|
May 28, 2018
Implementing Motor Unit Number Index (MUNIX) in a large clinical trial: Real world experience from 27 centres
Christoph Neuwirth, Nathalie Braun, Kristl G Claeys, et al.
Brain : a Journal of Neurology
|
March 13, 2023
Anoctamin-5 related muscle disease: clinical and genetic findings in a large European cohort
Alexander de Bruyn, Federica Montagnese, Sonja Holm-Yildiz, et al.
Brain : a Journal of Neurology
|
January 18, 2018
Hot-spot KIF5A mutations cause familial ALS
David Brenner, Rüstem Yilmaz, Kathrin Müller, et al.
Orphanet Journal of Rare Diseases
|
February 14, 2024
EURO-NMD registry: federated FAIR infrastructure, innovative technologies and concepts of a patient-centred registry for rare neuromuscular disorders
Antonio Atalaia, Dagmar Wandrei, Nawel Lalout, et al.
Nature Communications
|
March 29, 2019
Myoglobinopathy is an adult-onset autosomal dominant myopathy with characteristic sarcoplasmic inclusions
Montse Olivé, Martin Engvall, Gianina Ravenscroft, et al.
Brain : a Journal of Neurology
|
May 23, 2006
MFN2 mutation distribution and genotype/phenotype correlation in Charcot-Marie-Tooth type 2
Kristien Verhoeven, Kristl G Claeys, Stephan Züchner, et al.
Annals of Clinical and Translational Neurology
|
December 31, 2025
Whole-Body Pattern of Muscle Degeneration and Progression in Sarcoglycanopathies
Laura Costa-Comellas, Mauro Monforte, Angel Sanchez-Montañez, et al.
The Lancet. Neurology
|
October 5, 2007
Multicentre search for genetic susceptibility loci in sporadic epilepsy syndrome and seizure types: a case-control study
Gianpiero L Cavalleri, Michael E Weale, Kevin V Shianna, et al.
Brain : a Journal of Neurology
|
May 15, 2023
The emerging spectrum of fetal acetylcholine receptor antibody-related disorders (FARAD)
Nicholas M Allen, Mark O'Rahelly, Bruno Eymard, et al.
Page
of 24