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Journal of Neurology, Neurosurgery, and Psychiatry
|
June 5, 2016
Defining SOD1 ALS natural history to guide therapeutic clinical trial design
Taha Bali, Wade Self, Jingxia Liu, et al.
Cell
|
August 27, 2025
Molecular impact of antisense oligonucleotide therapy in C9orf72-associated ALS
Zachary T McEachin, Mingee Chung, Sabrina A Stratton, 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.
Neurobiology of Aging
|
July 24, 2018
ALS-associated missense and nonsense TBK1 mutations can both cause loss of kinase function
Martina de Majo, Simon D Topp, Bradley N Smith, et al.
Annals of Neurology
|
January 3, 2021
The Effect of SMN Gene Dosage on ALS Risk and Disease Severity
Matthieu Moisse, Ramona A J Zwamborn, Joke van Vugt, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
February 13, 2025
Oligogenic structure of amyotrophic lateral sclerosis has genetic testing, counselling and therapeutic implications
Alfredo Iacoangeli, Allison A Dilliott, Ahmad Al Khleifat, et al.
Neuron
|
May 7, 2020
Chimeric Peptide Species Contribute to Divergent Dipeptide Repeat Pathology in c9ALS/FTD and SCA36
Zachary T McEachin, Tania F Gendron, Nisha Raj, et al.
Frontiers in Cellular Neuroscience
|
March 20, 2023
Large-scale analyses of CAV1 and CAV2 suggest their expression is higher in post-mortem ALS brain tissue and affects survival
Brett N Adey, Johnathan Cooper-Knock, Ahmad Al Khleifat, et al.
Brain : a Journal of Neurology
|
April 12, 2023
Genetic variability in sporadic amyotrophic lateral sclerosis
Sien Hilde Van Daele, Matthieu Moisse, Joke J F A van Vugt, et al.
Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration
|
December 14, 2017
Reconsidering the causality of TIA1 mutations in ALS
Rick A van der Spek, Wouter van Rheenen, Sara L Pulit, et al.
Page
of 67
Search research articles
Search
Showing results (621-630 of 667) with videos related to
Sort By:
Page
of 67
Journal of Neurology, Neurosurgery, and Psychiatry
|
June 5, 2016
Defining SOD1 ALS natural history to guide therapeutic clinical trial design
Taha Bali, Wade Self, Jingxia Liu, et al.
Cell
|
August 27, 2025
Molecular impact of antisense oligonucleotide therapy in C9orf72-associated ALS
Zachary T McEachin, Mingee Chung, Sabrina A Stratton, 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.
Neurobiology of Aging
|
July 24, 2018
ALS-associated missense and nonsense TBK1 mutations can both cause loss of kinase function
Martina de Majo, Simon D Topp, Bradley N Smith, et al.
Annals of Neurology
|
January 3, 2021
The Effect of SMN Gene Dosage on ALS Risk and Disease Severity
Matthieu Moisse, Ramona A J Zwamborn, Joke van Vugt, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
February 13, 2025
Oligogenic structure of amyotrophic lateral sclerosis has genetic testing, counselling and therapeutic implications
Alfredo Iacoangeli, Allison A Dilliott, Ahmad Al Khleifat, et al.
Neuron
|
May 7, 2020
Chimeric Peptide Species Contribute to Divergent Dipeptide Repeat Pathology in c9ALS/FTD and SCA36
Zachary T McEachin, Tania F Gendron, Nisha Raj, et al.
Frontiers in Cellular Neuroscience
|
March 20, 2023
Large-scale analyses of CAV1 and CAV2 suggest their expression is higher in post-mortem ALS brain tissue and affects survival
Brett N Adey, Johnathan Cooper-Knock, Ahmad Al Khleifat, et al.
Brain : a Journal of Neurology
|
April 12, 2023
Genetic variability in sporadic amyotrophic lateral sclerosis
Sien Hilde Van Daele, Matthieu Moisse, Joke J F A van Vugt, et al.
Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration
|
December 14, 2017
Reconsidering the causality of TIA1 mutations in ALS
Rick A van der Spek, Wouter van Rheenen, Sara L Pulit, et al.
Page
of 67