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Article

Hyperkeratotic cutaneous vascular malformation associated with familial cerebral cavernous malformations (FCCM) with KRIT1/CCM1 mutation.

European journal of dermatology : EJD - 1 Jan 2000

Feldmeyer Laurence, Baumann-Vogel Heide, Tournier-Lasserve Elisabeth, Riant Florence, Jung Hans H, French Lars E, Kamarashev Jivko

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Share to Hemangioma, Cavernous, Central Nervous System
Share to Keratosis
Share to KRIT1 Protein

Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

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Identifiers

PMID: 24721395
DOI: 10.1684/ejd.2014.2280

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Hyperkeratotic cutaneous vascular malformation associated with familial cerebral cavernous malformations (FCCM) with KRIT1/CCM1 mutation.PMID 24721395Read ↗

Frequency and phenotypes of cutaneous vascular malformations in a consecutive series of 417 patients with familial cerebral cavernous malformations.Semantic proximity Read ↗

Cutaneous venous malformations in familial cerebral cavernomatosis caused by KRIT1 gene mutations.Semantic proximity Read ↗

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KRIT1 is mutated in hyperkeratotic cutaneous capillary-venous malformation associated with cerebral capillary malformation.Semantic proximity Read ↗

Clinical, neuroradiological and genetic findings in a cohort of patients with multiple Cerebral Cavernous Malformations.Semantic proximity Read ↗

Cerebral cavernous malformations as a disease of vascular permeability: from bench to bedside with caution.Semantic proximity Read ↗

Cerebral cavernous malformations associated with cutaneous angiokeratomas and hemangiomas.Semantic proximity Read ↗

A Novel MGC4607/CCM2 Gene Mutation Associated with Cerebral Spinal and Cutaneous Cavernous Angiomas.Semantic proximity Read ↗

KRIT1 Gene in Patients with Cerebral Cavernous Malformations: Clinical Features and Molecular Characterization of Novel Variants.Semantic proximity Read ↗

Cutaneous findings of familial cerebral cavernous malformation syndrome due to the common Hispanic mutation.Semantic proximity Read ↗

Cerebral cavernous malformations and unilateral moyamoya in a patient with a new mutation in the KRIT-1 /CCM1 gene.Semantic proximity Read ↗

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