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Mutations in Cu/Zn superoxide dismutase gene are associated with familial amyotrophic lateral sclerosis

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Nonparametric Statistical Methods

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1995 • 683 citations

Benefit of vitamin E, riluzole, and gababapentin in a transgenic model of familial amyotrophic lateral sclerosis

1996 • 654 citations

Superoxide Dismutase Activity, Oxidative Damage, and Mitochondrial Energy Metabolism in Familial and Sporadic Amyotrophic Lateral Sclerosis

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Superoxide dismutase 1 with mutations linked to familial amyotrophic lateral sclerosis possesses significant activity.

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Familial adult motor neuron disease: amyotrophic lateralsclerosis

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Linkage of a Gene Causing Familial Amyotrophic Lateral Sclerosis to Chromosome 21 and Evidence of Genetic-Locus Heterogeneity

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Onset, natural history and outcome in idiopathic adult motor neuron disease

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A rating scale for amyotrophic lateral sclerosis: Description and preliminary experience

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Linkage of recessive familial amyotrophic lateral sclerosis to chromosome 2q33–q35

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Rapid Communication: Cu/Zn Superoxide Dismutase Activity in Familial and Sporadic Amyotrophic Lateral Sclerosis

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The natural history of motoneuron loss in amyotrophic lateral sclerosis

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Duration of amyotrophic lateral sclerosis is age dependent

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Merritt's Textbook of Neurology

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Incidence and Prevalence of Amyotrophic Lateral Sclerosis in Harris County, Texas, 1985-1988

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Survival prediction in amyotrophic lateral sclerosis

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Familial amyotrophic lateral sclerosis (ALS) in Japan associated with H46R mutation in superoxide dismutase gene: A possible new subtype of familial ALS

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Variance of age at onset in a Japanese family with amyotrophic lateral sclerosis associated with a novel cu/zn superoxide dismutase mutation

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Familial amyotrophic lateral sclerosis with a mutation in the Cu/Zn superoxide dismutase gene

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SOD1 missense mutation in an Italian family with ALS

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Superoxide dismutase in familial amyotrophic lateral sclerosis: models for gain of function

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A New Variant Cu/Zn Superoxide Dismutase (Val7→Glu) Deduced from Lymphocyte mRNA Sequences from Japanese Patients with Familial Amyotrophic Lateral Sclerosis

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Spinal cord TRH deficiency is associated with incomplete recovery of denervated muscle in the rat

1988 • 26 citations

A novel point mutation in the Cu/Zn superoxide dismutase gene in a patient with familial amyotrophic lateral sclerosis

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Phenotypic and genotypic heterogeneity of dominantly inherited amyotrophic lateral sclerosis

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Superoxide dismutase (glu100 → gly) in a family with inherited motor neuron disease: detection of mutant superoxide dismutase activity and the presence of heterodimers

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Parental sex effect in familial amyotrophic lateral sclerosis

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Dinculeotide repeat polymorphism in the HOX4E locus

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Mortality risk stratification in amyotrophic lateral sclerosis

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