ALS Compendium
Identification of a FUS splicing mutation in a large family with amyotrophic lateral sclerosis
The effects of dexpramipexole (KNS-760704) in individuals with amyotrophic lateral sclerosis
Expanded GGGGCC hexanucleotide repeat in noncoding region of C9ORF72 causes chromosome 9p-linked FTD and ALS
Enhanced neuronal Met signalling levels in ALS mice delay disease onset
An ALS-associated mutation affecting TDP-43 enhances protein aggregation, fibril formation and neurotoxicity
Astrocytes from familial and sporadic ALS patients are toxic to motor neurons
CNS-targeted viral delivery of G-CSF in an animal model for ALS: improved efficacy and preservation of the neuromuscular unit
Long pre-mRNA depletion and RNA missplicing contribute to neuronal vulnerability from loss of TDP-43
A hexanucleotide repeat expansion in C9ORF72 is the cause of chromosome 9p21-linked ALS-FTD
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