Severe myoclonic epilepsy in infancy: clinical analysis and relation to SCN1A mutations in a Japanese cohort.

Advances in neurology

Volumn 95, Issue , 2005, Pages 103-117

  Oguni, Hirokazu ^a   Hayashi, Kitami ^a   Osawa, Makiko ^a   Awaya, Yutaka ^a   Fukuyama, Yukio ^a   Fukuma, Goryu ^a   Hirose, Shinichi ^a   Mitsudome, Akihisa ^a   Kaneko, Sunao ^a  

^a TOKYO WOMEN'S MEDICAL UNIVERSITY   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

NERVE PROTEIN; SODIUM CHANNEL; SODIUM CHANNEL, VOLTAGE GATED, TYPE I, ALPHA PROTEIN; SODIUM CHANNEL, VOLTAGE-GATED, TYPE I, ALPHA PROTEIN;

BODY TEMPERATURE; CASE REPORT; CLASSIFICATION; COHORT ANALYSIS; ELECTROENCEPHALOGRAPHY; ETHNOLOGY; FEMALE; GENETICS; GENOTYPE; HUMAN; INFANT; JAPAN; MALE; MENTAL DISEASE; METHODOLOGY; MUTATION; MYOCLONUS EPILEPSY; NEWBORN; PATHOPHYSIOLOGY; PHENOTYPE; PHYSIOLOGY; REFLEX EPILEPSY; REVIEW; TREATMENT OUTCOME;

BODY TEMPERATURE; COHORT STUDIES; ELECTROENCEPHALOGRAPHY; EPILEPSIES, MYOCLONIC; EPILEPSY, REFLEX; FEMALE; GENOTYPE; HUMANS; INFANT; INFANT, NEWBORN; JAPAN; MALE; MENTAL DISORDERS; MUTATION; NERVE TISSUE PROTEINS; PHENOTYPE; SODIUM CHANNELS; TREATMENT OUTCOME;

EID: 16544394846     PISSN: 00913952     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Review

References (46)