Mutations of the SCN1A gene in acute encephalopathy

Epilepsia

Volumn 53, Issue 3, 2012, Pages 558-564

  Saitoh, Makiko ^a   Shinohara, Mayu ^a   Hoshino, Hideki ^b   Kubota, Masaya ^b   Amemiya, Kaoru ^c   Takanashi, Jun Lchi ^d   Hwang, Su Kyeong ^e   Hirose, Shinichi ^e   Mizuguchi, Masashi ^a  

^a UNIVERSITY OF TOKYO   (Japan)

^b NATIONAL CENTER FOR CHILD HEALTH AND DEVELOPMENT   (Japan)

^c Tokyo Metropolitan Hachioji Children's Hospital   (Japan)

^d KAMEDA MEDICAL CENTER   (Japan)

^e FUKUOKA UNIVERSITY   (Japan)

Author keywords

Acute encephalopathy status epilepticus; Ion channel gene defect; SCN1A; Seizure susceptibility

Indexed keywords

AMINOTRANSFERASE; ANTICONVULSIVE AGENT; C REACTIVE PROTEIN; CARBAMAZEPINE; IMMUNOGLOBULIN; LACTATE DEHYDROGENASE; METHYLPREDNISOLONE; PHENYTOIN; SODIUM CHANNEL NAV1.1; THEOPHYLLINE; THIOPENTAL; VALPROIC ACID;

ACUTE BRAIN DISEASE; ARTICLE; ARTIFICIAL VENTILATION; ASTHMA; BLOOD EXAMINATION; BRAIN ATROPHY; BRAIN EDEMA; CEREBROSPINAL FLUID EXAMINATION; CHILD; COMA; COMPUTER ASSISTED TOMOGRAPHY; CONSCIOUSNESS DISORDER; CONTINUOUS INFUSION; CONTROLLED STUDY; CONVULSION; DIARRHEA; DRUG PULSE THERAPY; ELECTROENCEPHALOGRAPHY; ENZYME BLOOD LEVEL; EPILEPTIC STATE; FEBRILE CONVULSION; FEMALE; FEVER; FOCAL EPILEPSY; GASTROENTERITIS; GENERAL ANESTHESIA; GENETIC ASSOCIATION; GENETIC PREDISPOSITION; GESTATION PERIOD; GLASGOW COMA SCALE; HUMAN; LEIGH DISEASE; MAJOR CLINICAL STUDY; MALE; MENTAL DEFICIENCY; MYOCLONUS SEIZURE; NUCLEAR MAGNETIC RESONANCE IMAGING; NUCLEOTIDE SEQUENCE; POINT MUTATION; PRESCHOOL CHILD; PRIORITY JOURNAL; PROTEIN BLOOD LEVEL; QUADRIPLEGIA; RESPIRATORY TRACT INFECTION; SCHOOL CHILD; SEVERE MYOCLONIC EPILEPSY IN INFANCY; SPIKE WAVE; STUPOR; TONIC SEIZURE; VOMITING;

ASIAN CONTINENTAL ANCESTRY GROUP; CHILD; CHILD, PRESCHOOL; ENCEPHALITIS, VIRAL; EPILEPSY; FEMALE; GENETIC PREDISPOSITION TO DISEASE; GENETIC TESTING; HUMANS; INFANT; JAPAN; LEUKOENCEPHALITIS, ACUTE HEMORRHAGIC; MALE; NERVE TISSUE PROTEINS; POINT MUTATION; SODIUM CHANNELS;

EID: 84857643080     PISSN: 00139580     EISSN: 15281167     Source Type: Journal    
DOI: 10.1111/j.1528-1167.2011.03402.x     Document Type: Article

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