The expanding phenotype of GLUT1-deficiency syndrome

Brain and Development

Volumn 31, Issue 7, 2009, Pages 545-552

  Brockmann, Knut ^a  

^a UNIVERSITY OF GÖTTINGEN   (Germany)

Author keywords

Epilepsy; Glucose transport protein type 1; Hypoglycorrhachia; Ketogenic diet; Movement disorders; Paroxysmal dyskinesia

Indexed keywords

CARNITINE; GLUCOSE; GLUCOSE TRANSPORTER 1; THIOCTIC ACID;

ATAXIA; AUTOSOMAL DOMINANT INHERITANCE; CEREBROSPINAL FLUID ANALYSIS; CLINICAL FEATURE; DIAGNOSTIC VALUE; DIET SUPPLEMENTATION; DRUG MECHANISM; DYSKINESIA; DYSTONIA; ELECTROENCEPHALOGRAM; GENE MUTATION; GENOTYPE PHENOTYPE CORRELATION; GLUCOSE BLOOD LEVEL; GLUCOSE TRANSPORT; GLUCOSE TRANSPORTER 1 DEFICIENCY SYNDROME; HUMAN; KETOGENIC DIET; METABOLIC ENCEPHALOPATHY; MICROCEPHALY; NONHUMAN; NUCLEAR MAGNETIC RESONANCE IMAGING; PHENOTYPE; POSITRON EMISSION TOMOGRAPHY; REVIEW; SEIZURE; SPASTICITY; THERAPY EFFECT;

BRAIN; DYSKINESIAS; EPILEPSY; EXERCISE; GLUCOSE; GLUCOSE METABOLISM DISORDERS; GLUCOSE TRANSPORTER TYPE 1; HUMANS; KETOGENIC DIET; MOVEMENT DISORDERS; MUTATION; PHENOTYPE; SYNDROME; VIDEO RECORDING;

EID: 67649421265     PISSN: 03877604     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.braindev.2009.02.008     Document Type: Review

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