|
Volumn 74, Issue 11, 2010, Pages 909-912
|
Epilepsy and the natural history of Rett syndrome
|
Author keywords
[No Author keywords available]
|
Indexed keywords
METHYL CPG BINDING PROTEIN 2;
MECP2 PROTEIN, HUMAN;
ADULT;
ARTICLE;
CHILD;
CLINICAL ASSESSMENT;
CLINICAL EVALUATION;
CLINICAL TRIAL;
COMMUNICATION DISORDER;
DISEASE ASSOCIATION;
DISEASE SEVERITY;
EPILEPSY;
ETHNICITY;
FEMALE;
FUNDING;
HEALTH STATUS;
HUMAN;
INFANT;
MAJOR CLINICAL STUDY;
MUTATION;
NATIONAL HEALTH ORGANIZATION;
ONSET AGE;
PRESCHOOL CHILD;
PRIORITY JOURNAL;
RACE;
RETT SYNDROME;
SAMPLE SIZE;
SCHOOL CHILD;
SEIZURE;
WALKING DIFFICULTY;
ADOLESCENT;
AGE;
GENETIC PREDISPOSITION;
GENETICS;
HOSPITALIZATION;
MALE;
MIDDLE AGED;
PHENOTYPE;
REGRESSION ANALYSIS;
SEX DIFFERENCE;
ADOLESCENT;
ADULT;
AGE FACTORS;
AGE OF ONSET;
CHILD;
CHILD, PRESCHOOL;
EPILEPSY;
FEMALE;
GENETIC PREDISPOSITION TO DISEASE;
HUMANS;
INFANT;
MALE;
METHYL-CPG-BINDING PROTEIN 2;
MIDDLE AGED;
PHENOTYPE;
REGRESSION ANALYSIS;
RETT SYNDROME;
SEVERITY OF ILLNESS INDEX;
SEX FACTORS;
YOUNG ADULT;
|
EID: 77950503200
PISSN: 00283878
EISSN: 1526632X
Source Type: Journal
DOI: 10.1212/WNL.0b013e3181d6b852 Document Type: Article |
Times cited : (169)
|
References (7)
|