GLUT1 deficiency syndrome: An update

Revue Neurologique

Volumn 170, Issue 2, 2014, Pages 91-99

  Gras, D ^a,b   Roze, E ^a   Caillet, S ^c   Meneret A ^b,d   Doummar, D ^e   Billette De Villemeur, T ^e   Vidailhet, M ^b,c,d   Mochel, F ^b,c,d  

^a HÔPITAL ROBERT DEBRÉ   (France)

^b INSTITUT DU CERVEAU ET DE LA MOELLE ÉPINIÈRE   (France)

^c PITIÉ SALPÊTRIÈRE HOSPITAL   (France)

^d SORBONNE UNIVERSITÉ   (France)

^e ARMAND TROUSSEAU HOSPITAL   (France)

Author keywords

Epilepsy; Ketogenic diet; Mental retardation; Movement disorders; SLC2A1

Indexed keywords

GLUCOSE; GLUCOSE TRANSPORTER 1; THIOCTIC ACID; TRIHEPTANOIN;

CEREBROSPINAL FLUID LEVEL; DIET THERAPY; DIFFERENTIAL DIAGNOSIS; DISEASE ASSOCIATION; DISEASE SEVERITY; DYSKINESIA; GENERALIZED EPILEPSY; GENETICS; GLUCOSE TRANSPORTER 1 DEFICIENCY SYNDROME; HUMAN; KETOGENIC DIET; MENTAL DEFICIENCY; MICROCEPHALY; MOLECULAR DIAGNOSIS; MOTOR DYSFUNCTION; PATHOPHYSIOLOGY; PHENOTYPE; PROTEIN DEFICIENCY; REVIEW; SEIZURE;

EPILEPSY; ÉPILEPSIE; KETOGENIC DIET; MENTAL RETARDATION; MOUVEMENTS ANORMAUX; MOVEMENT DISORDERS; RETARD MENTAL; RÉGIME CÉTOGÈNE; SLC2A1;

CARBOHYDRATE METABOLISM, INBORN ERRORS; GLUCOSE TRANSPORTER TYPE 1; HUMANS; KETOGENIC DIET; MONOSACCHARIDE TRANSPORT PROTEINS; PHENOTYPE; THIOCTIC ACID; TRIGLYCERIDES;

EID: 84896709935     PISSN: 00353787     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.neurol.2013.09.005     Document Type: Review

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