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familial amyotrophic lateral sclerosis


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'familial amyotrophic lateral sclerosis' can also refer to...

familial amyotrophic lateral sclerosis

familial amyotrophic lateral sclerosis (FALS)

NEK1 mutations in familial amyotrophic lateral sclerosis

Cortical hyperexcitability may precede the onset of familial amyotrophic lateral sclerosis

Familial versus sporadic amyotrophic lateral sclerosis—a false dichotomy?

The unfolded protein response in familial amyotrophic lateral sclerosis

Are CHCHD10 mutations indeed associated with familial amyotrophic lateral sclerosis?

Reply: Mutations in the CHCHD10 gene are a common cause of familial amyotrophic lateral sclerosis

Mitochondrial dysfunction in a cell culture model of familial amyotrophic lateral sclerosis

Familial frontotemporal dementia and amyotrophic lateral sclerosis associated with the C9ORF72 hexanucleotide repeat

Mutations in the CHCHD10 gene are a common cause of familial amyotrophic lateral sclerosis

Reply: Are CHCHD10 mutations indeed associated with familial amyotrophic lateral sclerosis?

Gain-of-function profilin 1 mutations linked to familial amyotrophic lateral sclerosis cause seed-dependent intracellular TDP-43 aggregation

Familial amyotrophic lateral sclerosis with frontotemporal dementia is linked to a locus on chromosome 9p13.2–21.3

Clinical characteristics of patients with familial amyotrophic lateral sclerosis carrying the pathogenic GGGGCC hexanucleotide repeat expansion of C9ORF72

Familial amyotrophic lateral sclerosis-linked SOD1 mutants perturb fast axonal transport to reduce axonal mitochondria content

Functional alterations of the ubiquitin-proteasome system in motor neurons of a mouse model of familial amyotrophic lateral sclerosis†

Variation in the Biochemical/Biophysical Properties of Mutant Superoxide Dismutase 1 Enzymes and the Rate of Disease Progression in Familial Amyotrophic Lateral Sclerosis Kindreds

Oxidative stress causes abnormal accumulation of familial amyotrophic lateral sclerosis-related mutant SOD1 in transgenic Caenorhabditis elegans

 

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The hereditary form of amyotrophic lateral sclerosis (ALS) (q.v.). Five to ten percent of the cases of ALS are hereditary and about 20% of these are due to SOD mutations. See superoxide dismutase.

Subjects: Genetics and Genomics.


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