(Q34554938)

3 August 2017

title

Familial cavernous malformations of the central nervous system. A clinical and genetic study of 15 German families (English)

1 reference

3 August 2017

16

Rouleau GA

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3 August 2017

Siegel AM

1

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3 August 2017

Bertalanffy H

2

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3 August 2017

Dichgans JJ

3

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3 August 2017

Elger CE

4

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3 August 2017

Hopf H

5

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3 August 2017

Hopf N

6

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3 August 2017

Keidel M

7

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3 August 2017

Kleider A

8

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3 August 2017

Nowak G

9

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3 August 2017

Pfeiffer RA

10

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3 August 2017

Schramm J

11

1 reference

3 August 2017

Spuck S

12

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3 August 2017

Stefan H

13

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3 August 2017

Sure U

14

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3 August 2017

Baumann CR

15

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3 August 2017

Verlaan DJ

17

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3 August 2017

Andermann E

18

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3 August 2017

Andermann F

19

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3 August 2017

publication date

1 February 2005

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3 August 2017

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3 August 2017

volume

76

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3 August 2017

issue

2

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3 August 2017

page(s)

175-180

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

3 August 2017

cites work

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FS00115-004-1779-3

Cerebral cavernous malformations: mutations in Krit1

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FS00115-004-1779-3

CCM1 mutation screen of sporadic cases with cerebral cavernous malformations

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FS00115-004-1779-3

[131 cases of cavernous angioma (cavernomas) of the CNS, discovered by retrospective analysis of 24,535 autopsies]

21 January 2018

1 reference

12 December 2020

Association of Krev-1/rap1a with Krit1, a novel ankyrin repeat-containing protein encoded by a gene mapping to 7q21-22

1 reference

12 December 2020

Mutations in the gene encoding KRIT1, a Krev-1/rap1a binding protein, cause cerebral cavernous malformations (CCM1)

1 reference

12 December 2020

Cerebral cavernous malformations. Incidence and familial occurrence

1 reference

12 December 2020

Genetic heterogeneity of inherited cerebral cavernous malformation

1 reference

12 December 2020

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

1 reference

12 December 2020

Multiple familial cavernous malformations evaluated over three generations with MR

1 reference

12 December 2020

Interaction of the integrin beta1 cytoplasmic domain with ICAP-1 protein

1 reference

12 December 2020

Multilocus linkage identifies two new loci for a mendelian form of stroke, cerebral cavernous malformation, at 7p15-13 and 3q25.2-27.

1 reference

12 December 2020

Trinucleotide repeats not the only cause of anticipation.

1 reference

12 December 2020

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

1 reference

12 December 2020

Cerebral cavernomas in the adult. Review of the literature and analysis of 72 surgically treated patients

1 reference

12 December 2020

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

1 reference

12 December 2020

Interaction between krit1 and icap1alpha infers perturbation of integrin beta1-mediated angiogenesis in the pathogenesis of cerebral cavernous malformation

1 reference

12 December 2020

Krit1 missense mutations lead to splicing errors in cerebral cavernous malformation

1 reference

12 December 2020

CCM1 gene mutations in families segregating cerebral cavernous malformations

1 reference

12 December 2020

Mutations in a gene encoding a novel protein containing a phosphotyrosine-binding domain cause type 2 cerebral cavernous malformations

1 reference

12 December 2020

Familial cavernous angiomas: natural history and genetic study over a 5-year period.

1 reference

12 December 2020

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

1 reference

12 December 2020

KRIT1 association with the integrin-binding protein ICAP-1: a new direction in the elucidation of cerebral cavernous malformations (CCM1) pathogenesis

1 reference

12 December 2020

ICAP-1, a novel beta1 integrin cytoplasmic domain-associated protein, binds to a conserved and functionally important NPXY sequence motif of beta1 integrin

1 reference

12 December 2020

De novo lesions in familial form of cerebral cavernous malformations: clinical and MR features in 29 non-Hispanic families

1 reference

12 December 2020

CCM2 mutations account for 13% of cases in a large collection of kindreds with hereditary cavernous malformations

1 reference

12 December 2020

Truncating mutations in CCM1, encoding KRIT1, cause hereditary cavernous angiomas

1 reference

12 December 2020

Endothelial proliferation, neoangiogenesis, and potential de novo generation of cerebrovascular malformations

1 reference

12 December 2020

Anticipation in familial cavernous angioma: ascertainment bias or genetic cause.

1 reference

12 December 2020

Cavernous angiomas of the nervous system in Italy: clinical and genetic study

1 reference

12 December 2020

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

1 reference

12 December 2020

Natural history of the cavernous angioma

1 reference

12 December 2020

Familial cavernous angioma: an unknown, known disease

1 reference

12 December 2020

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

1 reference

12 December 2020

Treatment-induced neoangiogenesis in cerebral arteriovenous malformations.

1 reference

12 December 2020

An analysis of the natural history of cavernous angiomas

1 reference

12 December 2020

Cavernous haemangiomas (angiomas) of the brain: clinically significant lesions

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

Anticipation in familial cavernous angioma: a study of 52 families from International Familial Cavernous Angioma Study. IFCAS Group.

1 reference

12 December 2020

Linkage to the CCM2 locus and genetic heterogeneity in familial cerebral cavernous malformation

1 reference

12 December 2020

10.1007/S00115-004-1779-3

Identifiers

DOI

1 reference

Dimensions Publication ID

3 August 2017

1001057395

0 references

1 reference