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Neurobiology of Aging
|
December 15, 2022
Whole genome sequencing analysis reveals post-zygotic mutation variability in monozygotic twins discordant for amyotrophic lateral sclerosis
Gijs H P Tazelaar, Paul J Hop, Meinie Seelen, et al.
Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration
|
July 15, 2016
Multicenter validation of CSF neurofilaments as diagnostic biomarkers for ALS
Patrick Oeckl, Claude Jardel, François Salachas, et al.
Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration
|
May 31, 2023
COURAGE-ALS: a randomized, double-blind phase 3 study designed to improve participant experience and increase the probability of success
Jeremy M Shefner, Ammar Al-Chalabi, Jinsy A Andrews, 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.
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.
Neurobiology of Aging
|
October 22, 2018
Association of NIPA1 repeat expansions with amyotrophic lateral sclerosis in a large international cohort
Gijs H P Tazelaar, Annelot M Dekker, Joke J F A van Vugt, et al.
Brain Communications
|
September 21, 2020
<i>ATXN1</i> repeat expansions confer risk for amyotrophic lateral sclerosis and contribute to TDP-43 mislocalization
Gijs H P Tazelaar, Steven Boeynaems, Mathias De Decker, et al.
Page
of 24
Search research articles
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Showing results (211-220 of 238) with videos related to
Sort By:
Page
of 24
Neurobiology of Aging
|
December 15, 2022
Whole genome sequencing analysis reveals post-zygotic mutation variability in monozygotic twins discordant for amyotrophic lateral sclerosis
Gijs H P Tazelaar, Paul J Hop, Meinie Seelen, et al.
Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration
|
July 15, 2016
Multicenter validation of CSF neurofilaments as diagnostic biomarkers for ALS
Patrick Oeckl, Claude Jardel, François Salachas, et al.
Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration
|
May 31, 2023
COURAGE-ALS: a randomized, double-blind phase 3 study designed to improve participant experience and increase the probability of success
Jeremy M Shefner, Ammar Al-Chalabi, Jinsy A Andrews, 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.
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.
Neurobiology of Aging
|
October 22, 2018
Association of NIPA1 repeat expansions with amyotrophic lateral sclerosis in a large international cohort
Gijs H P Tazelaar, Annelot M Dekker, Joke J F A van Vugt, et al.
Brain Communications
|
September 21, 2020
<i>ATXN1</i> repeat expansions confer risk for amyotrophic lateral sclerosis and contribute to TDP-43 mislocalization
Gijs H P Tazelaar, Steven Boeynaems, Mathias De Decker, et al.
Page
of 24