(Q48773459)

15 February 2018

title

Familial cerebral cavernous malformation: report of a further Italian family. (English)

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15 February 2018

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2

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15 February 2018

Silvana Penco

8

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15 February 2018

Serena Nannucci

object named as

Serena Nannucci

1

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author name string

Anna Poggesi

3

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15 February 2018

Laura Ciolli

4

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15 February 2018

Maria Cristina Patrosso

5

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15 February 2018

Alessandro Marocchi

6

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15 February 2018

Domenico Inzitari

7

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15 February 2018

Leonardo Pantoni

9

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15 February 2018

publication date

30 January 2009

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15 February 2018

published in

Neurological Sciences

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15 February 2018

volume

30

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15 February 2018

issue

2

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15 February 2018

page(s)

143-147

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15 February 2018

https://scigraph.springernature.com/pub.10.1007/s10072-009-0020-3

exact match

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cites work

Familial cavernous angiomas

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FS10072-009-0020-3

Cerebral cavernous malformations. Incidence and familial occurrence

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FS10072-009-0020-3

Molecular genetic investigations in the CCM1 gene in sporadic cerebral cavernomas

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FS10072-009-0020-3

[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

An association between autosomal dominant cerebral cavernomas and a distinctive hyperkeratotic cutaneous vascular malformation in 4 families.

1 reference

12 December 2020

Mutations within the MGC4607 gene cause cerebral cavernous malformations

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

Identification of two novel mutations and of a novel critical region in the KRIT1 gene.

1 reference

12 December 2020

Highly variable penetrance in subjects affected with cavernous cerebral angiomas (CCM) carrying novel CCM1 and CCM2 mutations.

1 reference

12 December 2020

Familial form of intracranial cavernous angioma: MR imaging findings in 51 families. French Society of Neurosurgery

1 reference

12 December 2020

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

1 reference

12 December 2020

Frequency of retinal cavernomas in 60 patients with familial cerebral cavernomas: a clinical and genetic study

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

The natural history of familial cerebral cavernomas: a retrospective MRI study of 40 patients

1 reference

12 December 2020

Genetics of cavernous angiomas

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12 December 2020

The MRI appearance of cavernous malformations (angiomas).

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

Multiple cerebral cavernous malformations associated with extracranial mesenchymal anomalies

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12 December 2020

Cerebral cavernous malformation: new molecular and clinical insights

1 reference

12 December 2020

Different spectra of genomic deletions within the CCM genes between Italian and American CCM patient cohorts

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

Low frequency of PDCD10 mutations in a panel of CCM3 probands: potential for a fourth CCM locus

1 reference

12 December 2020

Familial cerebral cavernous angiomas: clinical and radiologic studies

1 reference

12 December 2020

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

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12 December 2020

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

1 reference

12 December 2020

Cavernous angiomas of the central nervous system

1 reference

12 December 2020

Mutations within the programmed cell death 10 gene cause cerebral cavernous malformations

1 reference

12 December 2020

Vertebral and spinal cavernous angiomas associated with familial cerebral cavernous malformation

1 reference

12 December 2020

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

12 December 2020

Natural history of the cavernous angioma.

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

Identification of a novel KRIT1 mutation in an Italian family with cerebral cavernous malformation by the protein truncation test

1 reference

12 December 2020

Spectrum and expression analysis of KRIT1 mutations in 121 consecutive and unrelated patients with Cerebral Cavernous Malformations.

1 reference

12 December 2020

An analysis of the natural history of cavernous angiomas.

1 reference

12 December 2020

Clinical, magnetic resonance imaging, and genetic study of 5 Italian families with cerebral cavernous malformation

1 reference

12 December 2020

Cerebral cavernous angiomas in the first year of life

1 reference

12 December 2020

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

1 reference

12 December 2020

CCM1 and CCM2 protein interactions in cell signaling: implications for cerebral cavernous malformations pathogenesis

1 reference

12 December 2020

Intramedullary cavernous angioma of the spinal cord in a pediatric patient, with multiple cavernomas, familial occurrence and partial spontaneous regression: case report and review of the literature.

1 reference

12 December 2020

10.1007/S10072-009-0020-3

Identifiers

DOI

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15 February 2018

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15 February 2018