The relationship of spinal muscular atrophy to motor neuron disease: investigation of SMN and NAIP gene deletions in sporadic and familial ALS (Q73161770)

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scientific article published on 01 January 1997

Language	Label	Description	Also known as
English	The relationship of spinal muscular atrophy to motor neuron disease: investigation of SMN and NAIP gene deletions in sporadic and familial ALS	scientific article published on 01 January 1997

Statements

scholarly article

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9073029%20AND%20SRC:MED&resulttype=core&format=json

1 November 2019

The relationship of spinal muscular atrophy to motor neuron disease: investigation of SMN and NAIP gene deletions in sporadic and familial ALS (English)

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9073029%20AND%20SRC:MED&resulttype=core&format=json

1 November 2019

spinal muscular atrophy

1 reference

based on heuristic

inferred from title

amyotrophic lateral sclerosis

1 reference

based on heuristic

inferred from title

muscular atrophy

1 reference

based on heuristic

inferred from title

author name string

R W Orrell

1

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9073029%20AND%20SRC:MED&resulttype=core&format=json

1 November 2019

J J Habgood

2

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9073029%20AND%20SRC:MED&resulttype=core&format=json

1 November 2019

J S de Belleroche

3

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9073029%20AND%20SRC:MED&resulttype=core&format=json

1 November 2019

R J Lane

4

1 reference

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1 November 2019

publication date

1 January 1997

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1 November 2019

Journal of the Neurological Sciences

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9073029%20AND%20SRC:MED&resulttype=core&format=json

1 November 2019

145

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1 November 2019

1

1 reference

Europe PubMed Central

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1 November 2019

55-61

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9073029%20AND%20SRC:MED&resulttype=core&format=json

1 November 2019

Intrafamilial heterogeneity in hereditary motor neuron disease

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2896%2900240-7

7 January 2021

Werdnig-Hoffmann disease and chronic distal spinal muscular atrophy with apparent autosomal dominant inheritance

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2896%2900240-7

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/10.1016%2FS0022-510X%2896%2900240-7

7 January 2021

"Wetherbee Ail"; the inheritance of progressive muscular atrophy as a dominant trait in two New England families

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2896%2900240-7

7 January 2021

SMN gene deletions in adult-onset spinal muscular atrophy

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2896%2900240-7

7 January 2021

The Brown-Vialetto-van Laere syndrome: a case report and literature review

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2896%2900240-7

7 January 2021

Familial amyotrophic lateral sclerosis/motor neurone disease (FALS): a review of current developments

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2896%2900240-7

7 January 2021

Familial amyotrophic lateral sclerosis occurring in 4 generations. Report of a case

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2896%2900240-7

7 January 2021

Chronic asymmetrical spinal muscular atrophy

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2896%2900240-7

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2896%2900240-7

7 January 2021

Hereditary motor peripheral neuropathy predominantly affecting the arms

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2896%2900240-7

7 January 2021

Identification and characterization of a spinal muscular atrophy-determining gene

1 reference

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7 January 2021

Familial adult motor neuron disease: amyotrophic lateral sclerosis

1 reference

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7 January 2021

Phenotypic heterogeneity of spinal muscular atrophy mapping to chromosome 5q11.2-13.3 (SMA 5q).

1 reference

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7 January 2021

Distal chronic spinal muscular atrophy involving the hands

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2896%2900240-7

7 January 2021

A clinical and genetic study of spinal muscular atrophy of adult onset: the autosomal recessive form as a discrete disease entity

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2896%2900240-7

7 January 2021

Classification of spinal muscular atrophies

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2896%2900240-7

7 January 2021

Clinical variability of autosomal dominant spinal muscular atrophy

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2896%2900240-7

7 January 2021

The gene for neuronal apoptosis inhibitory protein is partially deleted in individuals with spinal muscular atrophy

1 reference

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7 January 2021

Lower motor neuron degeneration and familial predisposition to colonic neoplasia in two adult siblings

1 reference

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7 January 2021

Adult-onset motor neuron disease and infantile Werdnig-Hoffmann disease (spinal muscular atrophy type 1) in the same family

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2896%2900240-7

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/10.1016%2FS0022-510X%2896%2900240-7

7 January 2021

Linkage analysis of distal hereditary motor neuropathy type II (distal HMN II) in a single pedigree

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2896%2900240-7

7 January 2021

PCR-based DNA test to confirm clinical diagnosis of autosomal recessive spinal muscular atrophy

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2896%2900240-7

7 January 2021

Identifiers

10.1016/S0022-510X(96)00240-7

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9073029%20AND%20SRC:MED&resulttype=core&format=json

1 November 2019

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9073029%20AND%20SRC:MED&resulttype=core&format=json

1 November 2019

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