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High-frequency motor rehabilitation in amyotrophic lateral sclerosis: a randomized clinical trial.
Not available
S-EPMC6529833
|
biostudies-literature
Cite
Valosin-containing protein (VCP) mutations in sporadic amyotrophic lateral sclerosis.
Not available
S-EPMC3391327
|
biostudies-literature
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Effect of tauroursodeoxycholic acid on survival and safety in amyotrophic lateral sclerosis: a retrospective population-based cohort study.
Not available
S-EPMC10570688
|
biostudies-literature
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ATNX2 is not a regulatory gene in Italian amyotrophic lateral sclerosis patients with C9ORF72 GGGGCC expansion.
Not available
S-EPMC4775342
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biostudies-literature
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Epidemiological, Clinical and Genetic Features of ALS in the Last Decade: A Prospective Population-Based Study in the Emilia Romagna Region of Italy.
Not available
S-EPMC9031824
|
biostudies-literature
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HFE p.H63D polymorphism does not influence ALS phenotype and survival.
Not available
S-EPMC5183653
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biostudies-literature
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A hexanucleotide repeat expansion in C9ORF72 is the cause of chromosome 9p21-linked ALS-FTD.
Not available
S-EPMC3200438
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biostudies-literature
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Mutations in the Matrin 3 gene cause familial amyotrophic lateral sclerosis.
Not available
S-EPMC4000579
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biostudies-literature
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