Epilepsy, energy deficiency and new therapeutic approaches including diet

Pharmacology and Therapeutics

Volumn 144, Issue 2, 2014, Pages 192-201

  Reid, Christopher A ^a   Mullen, Saul ^a   Kim, Tae Hwan ^a   Petrou, Steven ^a  

^a UNIVERSITY OF MELBOURNE   (Australia)

Author keywords

Epilepsy; Glucose; GLUT1 deficiency; Ketogenic diet; Metabolism

Indexed keywords

ADENOSINE TRIPHOSPHATASE (POTASSIUM SODIUM); ADENOSINE TRIPHOSPHATE; ADENOSINE TRIPHOSPHATE SENSITIVE POTASSIUM CHANNEL; CREATINE; DEOXYGLUCOSE; GLUCOSE; GLUCOSE TRANSPORTER 1; GLUTAMIC ACID; LACTIC ACID; POLYUNSATURATED FATTY ACID; PURINERGIC RECEPTOR; ADENOSINE TRIPHOSPHATASE; GLUCOSE TRANSPORTER;

ANAPLEROSIS; ARTICLE; ASTROCYTE; CITRIC ACID CYCLE; DISORDERS OF MITOCHONDRIAL FUNCTIONS; ENERGY DEFICIENCY; ENVIRONMENTAL FACTOR; EPILEPSY; GENETIC SUSCEPTIBILITY; GLUCOSE BRAIN LEVEL; GLUCOSE METABOLISM; GLYCEMIC INDEX; GLYCOLYSIS; HUMAN; KETOGENIC DIET; METABOLIC DISORDER; MOLECULAR DYNAMICS; NERVE CELL EXCITABILITY; NONHUMAN; PROTEIN TRANSPORT; SEIZURE SUSCEPTIBILITY; TONIC CLONIC SEIZURE; BIOSYNTHESIS; CALORIC INTAKE; COMPLICATION; DEFICIENCY; DIET THERAPY; METABOLISM; PATHOPHYSIOLOGY; PROCEDURES;

ADENOSINE TRIPHOSPHATASES; ADENOSINE TRIPHOSPHATE; ASTROCYTES; CREATINE; ENERGY INTAKE; EPILEPSY; GLUCOSE; GLUCOSE TRANSPORT PROTEINS, FACILITATIVE; HUMANS; KATP CHANNELS; KETOGENIC DIET; METABOLIC DISEASES; MITOCHONDRIAL DISEASES;

EID: 84907891697     PISSN: 01637258     EISSN: 1879016X     Source Type: Journal    
DOI: 10.1016/j.pharmthera.2014.06.001     Document Type: Review

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