Mitochondrial disorders and epilepsy

Revue Neurologique

Volumn 170, Issue 5, 2014, Pages 375-380

  Desguerre, I ^a   Hully, M ^a   Rio, M ^a   Nabbout, R ^a  

^a HÔPITAL NECKER ENFANTS MALADES   (France)

Author keywords

Alpers syndrome; Epilepsy; Ketogen diet; Mitochondrial disorders; Respiratory chain deficiency

Indexed keywords

ETIRACETAM; GABAPENTIN; HARKOSERIDE; LAMOTRIGINE; MITOCHONDRIAL DNA; VALPROIC ACID; DNA DIRECTED DNA POLYMERASE; POLG PROTEIN, HUMAN; UBIQUINONE;

ACUTE LIVER FAILURE; ARTICLE; DISEASE SEVERITY; DISORDERS OF MITOCHONDRIAL FUNCTIONS; ENERGY; EPILEPSY; EPILEPTIC STATE; FATALITY; FOCAL EPILEPSY; GENE MUTATION; HUMAN; INFANTILE SPASM; KETOGENIC DIET; MYOCLONUS EPILEPSY; NERVE CELL NECROSIS; ONSET AGE; PHENOTYPE; PROGNOSIS; ADULT; ATAXIA; CHILD; COMPLICATION; DEFICIENCY; GENETICS; MITOCHONDRIAL DISEASES; MUSCLE WEAKNESS; MUTATION; SCHILDER DISEASE;

ADULT; ATAXIA; CHILD; DIFFUSE CEREBRAL SCLEROSIS OF SCHILDER; DNA-DIRECTED DNA POLYMERASE; EPILEPSY; HUMANS; MITOCHONDRIAL DISEASES; MUSCLE WEAKNESS; MUTATION; PHENOTYPE; UBIQUINONE;

EID: 84901243768     PISSN: 00353787     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.neurol.2014.03.010     Document Type: Article

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