Allelic variations of glut-1 deficiency syndrome: The Chinese experience

Pediatric Neurology

Volumn 47, Issue 1, 2012, Pages 30-34

  Liu, Yanyan ^a,b   Bao, Xinhua ^a   Wang, Dong ^c   Fu, Na ^a   Zhang, Xiaoying ^a   Cao, Guangna ^a   Song, Fuying ^b   Wang, Shuang ^a   Zhang, Yuehua ^a   Qin, Jiong ^a   Yang, Hong ^c   Engelstad, Kristin ^c   De Vivo, Darryl C ^c   Wu, Xiru ^a  

^a PEKING UNIVERSITY FIRST HOSPITAL   (China)

^b Capital Children Hospital   (China)

^c Columbia University ^*  (United States)

Author keywords

[No Author keywords available]

Indexed keywords

GLUCOSE; GLUCOSE TRANSPORTER 1;

AMINO ACID SUBSTITUTION; ARTICLE; ATAXIA; BEHAVIOR DISORDER; CASE REPORT; CEREBROSPINAL FLUID LEVEL; CHILD; CHINESE; DEMYELINATION; DIAGNOSTIC TEST; DIET RESTRICTION; EARLY DIAGNOSIS; ELECTROENCEPHALOGRAM; ELECTROENCEPHALOGRAPHY; ERYTHROCYTE; EXERCISE TOLERANCE; FEMALE; FOLLOW UP; GENE; GENE DELETION; GENE MUTATION; GLUCOSE BLOOD LEVEL; GLUCOSE CEREBROSPINAL FLUID LEVEL; GLUCOSE TRANSPORT SYSTEM; GLUCOSE TRANSPORTER 1 DEFICIENCY SYNDROME; HUMAN; HUMAN CELL; INFANT; KETOGENIC DIET; MALE; MEAL; MUTATIONAL ANALYSIS; NEUROIMAGING; NUCLEAR MAGNETIC RESONANCE IMAGING; NUTRITIONAL INTOLERANCE; PRESCHOOL CHILD; PRIORITY JOURNAL; PROTEIN DEFICIENCY; SCHOOL CHILD; SLC2A1 GENE; WEAKNESS;

ASIAN CONTINENTAL ANCESTRY GROUP; CHILD; ELECTROENCEPHALOGRAPHY; ERYTHROCYTES; FEMALE; FOLLOW-UP STUDIES; GLUCOSE; GLUCOSE TRANSPORTER TYPE 1; HUMANS; KETOGENIC DIET; MAGNETIC RESONANCE IMAGING; MALE; METABOLISM, INBORN ERRORS; MODELS, MOLECULAR; MUTATION;

EID: 84862538285     PISSN: 08878994     EISSN: 18735150     Source Type: Journal    
DOI: 10.1016/j.pediatrneurol.2012.04.010     Document Type: Article

References (16)

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