(Q71230071)

English

Counting strokes

scientific article published on 01 August 1996

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scholarly article

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8696326%20AND%20SRC:MED&resulttype=core&format=json

17 October 2019

Counting strokes (English)

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8696326%20AND%20SRC:MED&resulttype=core&format=json

17 October 2019

author name string

Günel M

1

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17 October 2019

Lifton RP

2

1 reference

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17 October 2019

publication date

1 August 1996

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17 October 2019

Nature Genetics

1 reference

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17 October 2019

13

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17 October 2019

4

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17 October 2019

384-385

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17 October 2019

https://scigraph.springernature.com/pub.10.1038/ng0896-384

0 references

Chromosomal mapping of quantitative trait loci contributing to stroke in a rat model of complex human disease

1 reference

https://api.crossref.org/works/10.1038%2FNG0896-384

7 January 2021

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Blood pressure, stroke, and coronary heart disease. Part 1, Prolonged differences in blood pressure: prospective observational studies corrected for the regression dilution bias

1 reference

https://api.crossref.org/works/10.1038%2FNG0896-384

7 January 2021

based on heuristic

inferred from DOI database lookup

Molecular genetics of human blood pressure variation

1 reference

https://api.crossref.org/works/10.1038%2FNG0896-384

7 January 2021

based on heuristic

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A study of twins and stroke

1 reference

https://api.crossref.org/works/10.1038%2FNG0896-384

7 January 2021

based on heuristic

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Familial aggregation of stroke. The Framingham Study

1 reference

https://api.crossref.org/works/10.1038%2FNG0896-384

7 January 2021

based on heuristic

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Genetic aspects of cerebrovascular disease

1 reference

https://api.crossref.org/works/10.1038%2FNG0896-384

7 January 2021

based on heuristic

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Family history in patients with transient ischemic attacks

1 reference

https://api.crossref.org/works/10.1038%2FNG0896-384

7 January 2021

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Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy maps to chromosome 19q12

1 reference

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7 January 2021

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Mutation of the Alzheimer's disease amyloid gene in hereditary cerebral hemorrhage, Dutch type.

1 reference

https://api.crossref.org/works/10.1038%2FNG0896-384

7 January 2021

based on heuristic

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Familial intracranial aneurysms

1 reference

https://api.crossref.org/works/10.1038%2FNG0896-384

7 January 2021

based on heuristic

inferred from DOI database lookup

A founder mutation as a cause of cerebral cavernous malformation in Hispanic Americans

1 reference

https://api.crossref.org/works/10.1038%2FNG0896-384

7 January 2021

based on heuristic

inferred from DOI database lookup

Endoglin, a TGF-beta binding protein of endothelial cells, is the gene for hereditary haemorrhagic telangiectasia type 1

1 reference

https://api.crossref.org/works/10.1038%2FNG0896-384

7 January 2021

based on heuristic

inferred from DOI database lookup

Mutations in the activin receptor-like kinase 1 gene in hereditary haemorrhagic telangiectasia type 2.

1 reference

https://api.crossref.org/works/10.1038%2FNG0896-384

7 January 2021

based on heuristic

inferred from DOI database lookup

Identifiers

10.1038/NG0896-384

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8696326%20AND%20SRC:MED&resulttype=core&format=json

17 October 2019

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8696326%20AND%20SRC:MED&resulttype=core&format=json

17 October 2019

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