Genetics of sporadic ALS. (Q34315173)

1 August 2017

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title

Genetics of sporadic ALS. (English)

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amyotrophic lateral sclerosis

1 August 2017

main subject

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Andersen PM

1

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1 August 2017

publication date

1 March 2001

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Amyotrophic lateral sclerosis and other motor neuron disorders : official publication of the World Federation of Neurology, Research Group on Motor Neuron Diseases

1 August 2017

published in

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1 August 2017

volume

2 Suppl 1

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1 August 2017

page(s)

S37-41

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Longitudinal Gompertzian analysis of amyotrophic lateral sclerosis mortality in the U.S., 1977-1986: evidence for an inherently susceptible population subset

1 August 2017

cites work

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https://api.crossref.org/works/10.1080%2F14660820152415726

Longitudinal Gompertzian analysis of ALS mortality in England and Wales, 1963-1989: estimates of susceptibility in the general population

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F14660820152415726

Rising amyotrophic lateral sclerosis mortality in France 1968-1990: increased life expectancy and inter-disease competition as an explanation

21 January 2018

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https://api.crossref.org/works/10.1080%2F14660820152415726

Decline and rise of mortality from motor neuron disease in Spain, 1960-1989: demographic, environmental and competitive influences

21 January 2018

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https://api.crossref.org/works/10.1080%2F14660820152415726

Natural history of amyotrophic lateral sclerosis in a database population Validation of a scoring system and a model for survival prediction

21 January 2018

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https://api.crossref.org/works/10.1080%2F14660820152415726

Evidence of reduced DNA repair in amyotrophic lateral sclerosis brain tissue

21 January 2018

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https://api.crossref.org/works/10.1080%2F14660820152415726

Sequence variants in human neurofilament proteins: absence of linkage to familial amyotrophic lateral sclerosis

21 January 2018

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https://api.crossref.org/works/10.1080%2F14660820152415726

Deletions causing spinal muscular atrophy do not predispose to amyotrophic lateral sclerosis

21 January 2018

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https://api.crossref.org/works/10.1080%2F14660820152415726

Adult onset motor neuronopathy in the juvenile type of hexosaminidase A and B deficiency

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F14660820152415726

The EAAT2 (GLT-1) gene in motor neuron disease: absence of mutations in amyotrophic lateral sclerosis and a point mutation in patients with hereditary spastic paraplegia

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F14660820152415726

D90A heterozygosity in the SOD1 gene is associated with familial and apparently sporadic amyotrophic lateral sclerosis

21 January 2018

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https://api.crossref.org/works/10.1080%2F14660820152415726

Copper/zinc superoxide dismutase 1 and sporadic amyotrophic lateral sclerosis: analysis of 155 cases and identification of a novel insertion mutation.

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F14660820152415726

Cu/Zn superoxide dismutase gene mutations in amyotrophic lateral sclerosis: correlation between genotype and clinical features

21 January 2018

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https://api.crossref.org/works/10.1080%2F14660820152415726

Superoxide dismutase mutations in an unselected cohort of Scottish amyotrophic lateral sclerosis patients

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F14660820152415726

Evolution of CuZn superoxide dismutase and the Greek key beta-barrel structural motif

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F14660820152415726

How sensitive is PCR-SSCP?

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F14660820152415726

Analysis of chromosome 5q13 genes in amyotrophic lateral sclerosis: Homozygous naip deletion in a sporadic case

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F14660820152415726

10.1080/14660820152415726

21 January 2018

Identifiers

DOI

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1 August 2017

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