Search research articles
Contact Us
Filters
Showing results (161-170 of 167) with videos related to
Page
of 17
Sort By:
You have reached the last page of results.
This site can display upto 167 results.
Orphanet Journal of Rare Diseases
|
July 21, 2023
Digital health and Clinical Patient Management System (CPMS) platform utility for data sharing of neuromuscular patients: the Italian EURO-NMD experience
Fernanda Fortunato, Francesca Bianchi, Giulia Ricci, et al.
European Journal of Neurology
|
September 23, 2022
Effect of RNS60 in amyotrophic lateral sclerosis: a phase II multicentre, randomized, double-blind, placebo-controlled trial
Ettore Beghi, Elisabetta Pupillo, Elisa Bianchi, et al.
Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration
|
February 17, 2022
Clinical trials in pediatric ALS: a TRICALS feasibility study
Tessa Kliest, Ruben P A Van Eijk, Ammar Al-Chalabi, et al.
Cell Genomics
|
October 22, 2024
Mechanism-free repurposing of drugs for C9orf72-related ALS/FTD using large-scale genomic data
Sara Saez-Atienzar, Cleide Dos Santos Souza, Ruth Chia, et al.
Nature Genetics
|
July 26, 2016
Genome-wide association analyses identify new risk variants and the genetic architecture of amyotrophic lateral sclerosis
Wouter van Rheenen, Aleksey Shatunov, Annelot M Dekker, et al.
Neuron
|
March 24, 2018
Genome-wide Analyses Identify KIF5A as a Novel ALS Gene
Aude Nicolas, Kevin P Kenna, Alan E Renton, et al.
JAMA Neurology
|
August 30, 2021
Association of Variants in the SPTLC1 Gene With Juvenile Amyotrophic Lateral Sclerosis
Janel O Johnson, Ruth Chia, Danny E Miller, et al.
Page
of 17
Search research articles
Search
Showing results (161-170 of 167) with videos related to
Sort By:
Page
of 17
You have reached the last page of results.
This site can display upto 167 results.
Orphanet Journal of Rare Diseases
|
July 21, 2023
Digital health and Clinical Patient Management System (CPMS) platform utility for data sharing of neuromuscular patients: the Italian EURO-NMD experience
Fernanda Fortunato, Francesca Bianchi, Giulia Ricci, et al.
European Journal of Neurology
|
September 23, 2022
Effect of RNS60 in amyotrophic lateral sclerosis: a phase II multicentre, randomized, double-blind, placebo-controlled trial
Ettore Beghi, Elisabetta Pupillo, Elisa Bianchi, et al.
Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration
|
February 17, 2022
Clinical trials in pediatric ALS: a TRICALS feasibility study
Tessa Kliest, Ruben P A Van Eijk, Ammar Al-Chalabi, et al.
Cell Genomics
|
October 22, 2024
Mechanism-free repurposing of drugs for C9orf72-related ALS/FTD using large-scale genomic data
Sara Saez-Atienzar, Cleide Dos Santos Souza, Ruth Chia, et al.
Nature Genetics
|
July 26, 2016
Genome-wide association analyses identify new risk variants and the genetic architecture of amyotrophic lateral sclerosis
Wouter van Rheenen, Aleksey Shatunov, Annelot M Dekker, et al.
Neuron
|
March 24, 2018
Genome-wide Analyses Identify KIF5A as a Novel ALS Gene
Aude Nicolas, Kevin P Kenna, Alan E Renton, et al.
JAMA Neurology
|
August 30, 2021
Association of Variants in the SPTLC1 Gene With Juvenile Amyotrophic Lateral Sclerosis
Janel O Johnson, Ruth Chia, Danny E Miller, et al.
Page
of 17