(Q58477846)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18060566%20AND%20SRC:MED&resulttype=core&format=json

29 December 2019

title

Birth order and the genetics of amyotrophic lateral sclerosis (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18060566%20AND%20SRC:MED&resulttype=core&format=json

amyotrophic lateral sclerosis

29 December 2019

main subject

0 references

author

Christopher Shaw

4

1 reference

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29 December 2019

Ammar Al-Chalabi

7

1 reference

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29 December 2019

3

Diane McKenna-Yasek

1 reference

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29 December 2019

1

Umesh Vivekananda

1 reference

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29 December 2019

6

Robert H Brown

1 reference

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29 December 2019

author name string

Clare Johnston

2

1 reference

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29 December 2019

P Nigel Leigh

5

1 reference

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29 December 2019

publication date

19 December 2007

1 reference

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29 December 2019

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18060566%20AND%20SRC:MED&resulttype=core&format=json

29 December 2019

volume

255

1 reference

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29 December 2019

issue

1

1 reference

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29 December 2019

page(s)

99-102

1 reference

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https://scigraph.springernature.com/pub.10.1007/s00415-007-0709-2

29 December 2019

exact match

0 references

cites work

Parental age at child's birth and son's risk of prostate cancer. The Framingham Study.

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FS00415-007-0709-2

High rate of constitutional chromosomal rearrangements in apparently sporadic ALS

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FS00415-007-0709-2

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

21 January 2018

1 reference

12 December 2020

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

1 reference

12 December 2020

Phenotypic heterogeneity in motor neuron disease patients with CuZn-superoxide dismutase mutations in Scandinavia.

1 reference

12 December 2020

Spontaneous mutation and parental age in humans

1 reference

12 December 2020

Amyotrophic lateral sclerosis in an urban setting

1 reference

12 December 2020

On the origin of deletions and point mutations in Duchenne muscular dystrophy: most deletions arise in oogenesis and most point mutations result from events in spermatogenesis

1 reference

12 December 2020

?True? sporadic ALS associated with a novel SOD-1 mutation

1 reference

12 December 2020

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

1 reference

12 December 2020

The origins, patterns and implications of human spontaneous mutation

1 reference

12 December 2020

Parental age and mutation

1 reference

12 December 2020

Paternal age and the risk of congenital heart defects

1 reference

12 December 2020

Prolonged survival in motor neuron disease: a descriptive study of the King's database 1990-2002

1 reference

12 December 2020

10.1007/S00415-007-0709-2

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18060566%20AND%20SRC:MED&resulttype=core&format=json

29 December 2019

1 reference