(Q48322876)

10 February 2018

title

Hereditary cerebral cavernous angiomas: clinical and genetic features in 57 French families. Société Française de Neurochirurgie. (English)

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10 February 2018

Elisabeth Tournier-Lasserve

author

5

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10 February 2018

Sophie Laberge

object named as

S Laberge

2

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author name string

P Labauge

1

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10 February 2018

L Brunereau

3

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10 February 2018

C Levy

4

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10 February 2018

language of work or name

English

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publication date

1 December 1998

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10 February 2018

published in

The Lancet

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10 February 2018

volume

352

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10 February 2018

page(s)

1892-1897

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10 February 2018

issue

9144

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10 February 2018

An analysis of the natural history of cavernous angiomas.

cites work

1 reference

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Cerebral cavernous malformations. Incidence and familial occurrence

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7 January 2021

The natural history of familial cavernous malformations: results of an ongoing study

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2898%2903011-6

7 January 2021

A gene responsible for cavernous malformations of the brain maps to chromosome 7q

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2898%2903011-6

7 January 2021

Mapping a gene causing cerebral cavernous malformation to 7q11.2-q21

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https://api.crossref.org/works/10.1016%2FS0140-6736%2898%2903011-6

7 January 2021

A locus for cerebral cavernous malformations maps to chromosome 7q in two families

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7 January 2021

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

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7 January 2021

Linkage of the locus for cerebral cavernous hemangiomas to human chromosome 7q in four families of Mexican-American descent.

1 reference

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7 January 2021

Familial cerebral cavernous angioma: a gene localized to a 15-cM interval on chromosome 7q

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2898%2903011-6

7 January 2021

Refined localization of the cerebral cavernous malformation gene (CCM1) to a 4-cM interval of chromosome 7q contained in a well-defined YAC contig

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2898%2903011-6

7 January 2021

Familial cavernous malformations in a large French kindred: mapping of the gene to the CCM1 locus on chromosome 7q.

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https://api.crossref.org/works/10.1016%2FS0140-6736%2898%2903011-6

7 January 2021

Proposal for revised classification of epilepsies and epileptic syndromes. Commission on Classification and Terminology of the International League Against Epilepsy

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Progressive vision loss. A rare manifestation of familial cavernous angiomas.

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7 January 2021

Cavernous angioma: a review of 126 collected and 12 new clinical cases

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https://api.crossref.org/works/10.1016%2FS0140-6736%2898%2903011-6

7 January 2021

Familial cerebral cavernous angiomas: clinical and radiologic studies

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2898%2903011-6

7 January 2021

Factors predisposing to clinical disability in patients with cavernous malformations of the brain.

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2898%2903011-6

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The natural history of cerebral cavernous malformations

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2898%2903011-6

7 January 2021

10.1016/S0140-6736(98)03011-6

Identifiers

DOI

1 reference

10 February 2018

PubMed ID

9863787

1 reference

10 February 2018