(Q38334383)

2 September 2017

Identification of six novel SOD1 gene mutations in familial amyotrophic lateral sclerosis (English)

1 reference

amyotrophic lateral sclerosis

2 September 2017

0 references

8

Rouleau GA

1 reference

2 September 2017

Boukaftane Y

1

1 reference

2 September 2017

Khoris J

2

1 reference

2 September 2017

Moulard B

3

1 reference

2 September 2017

Salachas F

4

1 reference

2 September 2017

Meininger V

5

1 reference

2 September 2017

Malafosse A

6

1 reference

2 September 2017

Camu W

7

1 reference

2 September 2017

1 August 1998

1 reference

Canadian Journal of Neurological Sciences

2 September 2017

1 reference

2 September 2017

25

1 reference

2 September 2017

3

1 reference

2 September 2017

192-196

1 reference

Identification of a novel SOD1 mutation in an apparently sporadic amyotrophic lateral sclerosis patient and the detection of Ile113Thr in three others

2 September 2017

1 reference

https://api.crossref.org/works/10.1017%2FS0317167100034004

7 January 2021

Strand-separating conformational polymorphism analysis: efficacy of detection of point mutations in the human ornithine delta-aminotransferase gene

1 reference

https://api.crossref.org/works/10.1017%2FS0317167100034004

7 January 2021

Amyotrophic lateral sclerosis: Part 1. Clinical features, pathology, and ethical issues in management.

1 reference

https://api.crossref.org/works/10.1017%2FS0317167100034004

7 January 2021

Motor neuron degeneration in mice that express a human Cu,Zn superoxide dismutase mutation

1 reference

https://api.crossref.org/works/10.1017%2FS0317167100034004

7 January 2021

Autosomal recessive adult-onset amyotrophic lateral sclerosis associated with homozygosity for Asp90Ala CuZn-superoxide dismutase mutation. A clinical and genealogical study of 36 patients

1 reference

https://api.crossref.org/works/10.1017%2FS0317167100034004

7 January 2021

Amyotrophic lateral sclerosis associated with homozygosity for an Asp90Ala mutation in CuZn-superoxide dismutase

1 reference

https://api.crossref.org/works/10.1017%2FS0317167100034004

7 January 2021

Amyotrophic lateral sclerosis: Part 2. Etiopathogenesis

1 reference

https://api.crossref.org/works/10.1017%2FS0317167100034004

7 January 2021

Linkage of a gene causing familial amyotrophic lateral sclerosis to chromosome 21 and evidence of genetic-locus heterogeneity

1 reference

https://api.crossref.org/works/10.1017%2FS0317167100034004

7 January 2021

Zinc, a neurotoxin to cultured neurons, contaminates cycad flour prepared by traditional guamanian methods.

1 reference

https://api.crossref.org/works/10.1017%2FS0317167100034004

7 January 2021

Familial adult motor neuron disease: amyotrophic lateral sclerosis

1 reference

https://api.crossref.org/works/10.1017%2FS0317167100034004

7 January 2021

Hippocampal zinc thionein and pyridoxal phosphate modulate synaptic functions

1 reference

https://api.crossref.org/works/10.1017%2FS0317167100034004

7 January 2021

Amyotrophic lateral sclerosis and structural defects in Cu,Zn superoxide dismutase

1 reference

https://api.crossref.org/works/10.1017%2FS0317167100034004

7 January 2021

El Escorial World Federation of Neurology criteria for the diagnosis of amyotrophic lateral sclerosis. Subcommittee on Motor Neuron Diseases/Amyotrophic Lateral Sclerosis of the World Federation of Neurology Research Group on Neuromuscular Diseases a

1 reference

https://api.crossref.org/works/10.1017%2FS0317167100034004

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1017%2FS0317167100034004

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1017%2FS0317167100034004

7 January 2021

Mechanisms of selective motor neuron death in transgenic mouse models of motor neuron disease.

1 reference

https://api.crossref.org/works/10.1017%2FS0317167100034004

7 January 2021

Genetics of amyotrophic lateral sclerosis

1 reference

https://api.crossref.org/works/10.1017%2FS0317167100034004

7 January 2021

A frequent ala 4 to val superoxide dismutase-1 mutation is associated with a rapidly progressive familial amyotrophic lateral sclerosis

1 reference

https://api.crossref.org/works/10.1017%2FS0317167100034004

7 January 2021

Detection of polymorphisms of human DNA by gel electrophoresis as single-strand conformation polymorphisms

1 reference

https://api.crossref.org/works/10.1017%2FS0317167100034004

7 January 2021

An improved protocol for the analysis of SOD1 gene mutations, and a new mutation in exon 4.

1 reference

https://api.crossref.org/works/10.1017%2FS0317167100034004

7 January 2021

Zinc neurotoxicity in cortical cell culture

1 reference

https://api.crossref.org/works/10.1017%2FS0317167100034004

7 January 2021

10.1017/S0317167100034004

Identifiers

DOI

0 references

1 reference