Familial versus sporadic cavernous malformations: Differences in developmental venous anomaly association and lesion phenotype

American Journal of Neuroradiology

Volumn 31, Issue 2, 2010, Pages 377-382

  Petersen, T A ^a   Morrison, L A ^a   Schrader, R M ^a   Hart, Blaine L ^b  

^a UNIVERSITY OF NEW MEXICO HEALTH SCIENCES CENTER   (United States)

^b UNIVERSITY OF NEW MEXICO SCHOOL OF MEDICINE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

GADOLINIUM;

ADOLESCENT; ADULT; AGED; ARTICLE; BRAIN DAMAGE; CAVERNOUS SINUS; CEREBRAL CAVERNOUS MALFORMATION; CEREBROVASCULAR MALFORMATION; CEREBROVASCULAR SURGERY; CHILD; CONTROLLED STUDY; DEVELOPMENTAL DISORDER; DISEASE ASSOCIATION; FAMILY HISTORY; FEMALE; GENE MUTATION; HISPANIC; HUMAN; MAJOR CLINICAL STUDY; MALE; NEUROIMAGING; NUCLEAR MAGNETIC RESONANCE IMAGING; PATHOPHYSIOLOGY; PHENOTYPE; PRESCHOOL CHILD; RETROSPECTIVE STUDY; SCHOOL CHILD; UNITED STATES; VASCULAR LESION;

ADOLESCENT; ADULT; AGED; AGED, 80 AND OVER; CEREBRAL VEINS; CHILD; CHILD, PRESCHOOL; FEMALE; GENETIC PREDISPOSITION TO DISEASE; HEMANGIOMA, CAVERNOUS, CENTRAL NERVOUS SYSTEM; HUMANS; INFANT; MAGNETIC RESONANCE IMAGING; MALE; MICROTUBULE-ASSOCIATED PROTEINS; MIDDLE AGED; PHENOTYPE; PROTO-ONCOGENE PROTEINS; RETROSPECTIVE STUDIES; RISK FACTORS; YOUNG ADULT;

EID: 76749130195     PISSN: 01956108     EISSN: None     Source Type: Journal    
DOI: 10.3174/ajnr.A1822     Document Type: Article

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