Epilepsy and outcome in FOXG1-related disorders

Epilepsia

Volumn 55, Issue 8, 2014, Pages 1292-1300

  Seltzer, Laurie E ^a   Ma, Mandy ^b   Ahmed, Sohnee ^a   Bertrand, Mary ^c   Dobyns, William B ^d   Wheless, James ^e   Paciorkowski, Alex R ^a  

^a UNIVERSITY OF ROCHESTER MEDICAL CENTER   (United States)

^b UNIVERSITY AT BUFFALO   (United States)

^c WASHINGTON UNIVERSITY   (United States)

^d UNIVERSITY OF WASHINGTON   (United States)

^e UNIVERSITY OF TENNESSEE HEALTH SCIENCE CENTER   (United States)

Author keywords

14q12; Developmental outcome; Epilepsy; FOXG1; Infantile spasms

Indexed keywords

ANTICONVULSIVE AGENT;

ADOLESCENT; ADULT; ANTICONVULSANT THERAPY; ARTICLE; AUTISM; CHILD; CLINICAL ARTICLE; CLINICAL FEATURE; DISEASE SEVERITY; EPILEPSY; FEMALE; FOLLOW UP; FOXG1 GENE; FOXG1 RELATED DISORDER; GENE; GENE DELETION; GENE DUPLICATION; GENE MUTATION; GENE SEQUENCE; GENETIC DISORDER; HAND; HORMONAL THERAPY; HUMAN; INFANTILE SPASM; INTRACTABLE EPILEPSY; LANGUAGE DISABILITY; MALE; MEDICAL RECORD; MICROARRAY ANALYSIS; NERVE CELL DIFFERENTIATION; NEUROIMAGING; NEUROLOGIST; PRESCHOOL CHILD; PRIORITY JOURNAL; QUESTIONNAIRE; SCHOOL CHILD; SOCIAL BEHAVIOR; STANDARDIZATION; TELEPHONE INTERVIEW; YOUNG ADULT;

14Q12; DEVELOPMENTAL OUTCOME; EPILEPSY; FOXG1; INFANTILE SPASMS;

ADOLESCENT; ADULT; CHILD; CHILD, PRESCHOOL; COHORT STUDIES; EPILEPSY; FEMALE; FOLLOW-UP STUDIES; FORKHEAD TRANSCRIPTION FACTORS; HUMANS; INFANT; MALE; MUTATION; NERVE TISSUE PROTEINS; TREATMENT OUTCOME; YOUNG ADULT;

EID: 84905564999     PISSN: 00139580     EISSN: 15281167     Source Type: Journal    
DOI: 10.1111/epi.12648     Document Type: Article

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