Periventricular nodular heterotopia in patients with filamin-1 gene mutations: Neuroimaging findings

Pediatric Radiology

Volumn 30, Issue 11, 2000, Pages 748-755

  Poussaint, T Y ^a   Fox, J W ^b   Dobyns, W B ^c   Radtke, R ^d   Scheffer, I E ^e   Berkovic, S F ^e   Barnes, P D ^a   Huttenlocher, P R ^c   Walsh, C A ^b  

^a BOSTON CHILDREN S HOSPITAL   (United States)

^b HARVARD MEDICAL SCHOOL   (United States)

^c UNIVERSITY OF CHICAGO   (United States)

^d DUKE UNIVERSITY MEDICAL CENTER   (United States)

^e UNIVERSITY OF MELBOURNE   (Australia)

Author keywords

[No Author keywords available]

Indexed keywords

FILAMIN;

ADOLESCENT; ADULT; ARTICLE; AUTOSOMAL DOMINANT INHERITANCE; BRAIN DEVELOPMENT; BRAIN MALFORMATION; BRAIN SCINTISCANNING; CELL MIGRATION; CLINICAL ARTICLE; CLINICAL FEATURE; DATA ANALYSIS; FEMALE; GENE MUTATION; GENETIC ANALYSIS; GENETIC COUNSELING; GENETIC SUSCEPTIBILITY; HETEROTOPIA; HUMAN; IMAGE ANALYSIS; INFANT; INTELLIGENCE QUOTIENT; MALE; MEDICAL RECORD; NERVE CELL; NUCLEAR MAGNETIC RESONANCE IMAGING; PEDIGREE ANALYSIS; PRESCHOOL CHILD; PRIORITY JOURNAL; PROGENY; RETROSPECTIVE STUDY; REVIEW; RISK ASSESSMENT; SEIZURE; SEX DIFFERENCE; X CHROMOSOME LINKAGE;

EID: 0033736569     PISSN: 03010449     EISSN: None     Source Type: Journal    
DOI: 10.1007/s002470000312     Document Type: Article

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