Encephalopathy and SCN1A mutations

Epilepsia

Volumn 52, Issue 4, 2011, Pages

  Tang, Shan ^a   Lin, Jean Pierre ^a   Hughes, Elaine ^a   Siddiqui, Ata ^b   Lim, Ming ^a   Lascelles, Karine ^a  

^a ST THOMAS HOSPITAL   (United Kingdom)

^b GUY'S AND ST THOMAS' NHS FOUNDATION TRUST   (United Kingdom)

Author keywords

Cerebellar; Encephalopathy; GEFS; SCN1A; Sodium channel

Indexed keywords

AMOXICILLIN PLUS CLAVULANIC ACID; ANTIBIOTIC AGENT; CEFOTAXIME; CLOBAZAM; CLONAZEPAM; DIAZEPAM; ERYTHROMYCIN; ETIRACETAM; GENTAMICIN; LAMOTRIGINE; PARALDEHYDE; PHENYTOIN; PIPERACILLIN PLUS TAZOBACTAM; SODIUM CHANNEL NAV1.1; STIRIPENTOL; THIOPENTAL; VALPROIC ACID; VITAMIN K GROUP;

ADOLESCENT; ARTICLE; BRAIN ATROPHY; BRAIN DISEASE; BRAIN INJURY; BRAIN ISCHEMIA; CASE REPORT; CEREBELLUM DISEASE; CHILD; CHOREOATHETOSIS; COGNITIVE DEFECT; DETERIORATION; DISEASE COURSE; DYSTONIA; EPILEPSY; EPILEPTIC STATE; FEEDING BEHAVIOR; FOCAL EPILEPSY; FUNCTIONAL DISEASE; GENE MUTATION; HEPATORENAL SYNDROME; HUMAN; INFANT; LEARNING DISORDER; MALE; METABOLIC ACIDOSIS; MOTOR DYSFUNCTION; MUSCLE HYPOTONIA; NEUROIMAGING; NUCLEAR MAGNETIC RESONANCE IMAGING; PRESCHOOL CHILD; PRIORITY JOURNAL; RHABDOMYOLYSIS; SCHOOL CHILD; SEPSIS; TONIC CLONIC SEIZURE; WHITE MATTER;

BRAIN ISCHEMIA; CEREBELLAR DISEASES; CHILD, PRESCHOOL; EPILEPSY; FATAL OUTCOME; HUMANS; MALE; MENTAL RETARDATION; NERVE TISSUE PROTEINS; SODIUM CHANNELS; SPASMS, INFANTILE;

EID: 79953692382     PISSN: 00139580     EISSN: 15281167     Source Type: Journal    
DOI: 10.1111/j.1528-1167.2011.03019.x     Document Type: Article

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