Frequency and phenotypes of cutaneous vascular malformations in a consecutive series of 417 patients with familial cerebral cavernous malformations

Journal of the European Academy of Dermatology and Venereology

Volumn 23, Issue 9, 2009, Pages 1066-1072

  Sirvente, J ^a   Enjolras, O ^b   Wassef, M ^c   Tournier Lasserve, E ^c,d   Labauge, P ^a  

^a DEPARTMENT OF NEUROLOGY   (France)

^b ARMAND TROUSSEAU HOSPITAL   (France)

^c HÔPITAL LARIBOISIÈRE   (France)

^d INSERM   (France)

Author keywords

CCM; Cerebral cavernomas; Cutaneous lesions; HCCVM

Indexed keywords

ADULT; ARTICLE; BRAIN MALFORMATION; CAVERNOUS SINUS; CLINICAL ARTICLE; CLINICAL ASSESSMENT; CLINICAL FEATURE; CONGENITAL BLOOD VESSEL MALFORMATION; DISEASE CLASSIFICATION; FAMILIAL CEREBRAL CAVERNOUS MALFORMATION; FAMILIAL DISEASE; FAMILY HISTORY; GENE MUTATION; GENOTYPE PHENOTYPE CORRELATION; HISTOLOGY; HUMAN; NEUROLOGICAL COMPLICATION; NUCLEAR MAGNETIC RESONANCE IMAGING; PHENOTYPE; PRIORITY JOURNAL; SKIN BIOPSY;

APOPTOSIS REGULATORY PROTEINS; BIOPSY; CARRIER PROTEINS; CENTRAL NERVOUS SYSTEM VASCULAR MALFORMATIONS; HUMANS; MEMBRANE PROTEINS; MICROTUBULE-ASSOCIATED PROTEINS; MUTATION; PHENOTYPE; PREVALENCE; PROSPECTIVE STUDIES; PROTO-ONCOGENE PROTEINS; RETROSPECTIVE STUDIES; SKIN; SKIN DISEASES, VASCULAR; VASCULAR MALFORMATIONS;

EID: 68749122242     PISSN: 09269959     EISSN: 14683083     Source Type: Journal    
DOI: 10.1111/j.1468-3083.2009.03263.x     Document Type: Article

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