Disorders of glutamate metabolism

Mental Retardation and Developmental Disabilities Research Reviews

Volumn 7, Issue 4, 2001, Pages 287-295

  Kelly, Andrea ^a,b   Stanley, Charles A ^a,b  

^a UNIVERSITY OF PENNSYLVANIA   (United States)

^b CHILDREN S HOSPITAL OF PHILADELPHIA   (United States)

Author keywords

Glutamate dehydrogenase; Hyperammonemia; Hypoglycemia; Nesidioblastosis; Seizure disorders

Indexed keywords

GLUCOSE; GLUTAMIC ACID;

CHILD; CLINICAL ARTICLE; CONTROLLED STUDY; DISEASE ASSOCIATION; ENZYME ACTIVITY; ENZYME DEFICIENCY; FEMALE; GENE MUTATION; GLUCOSE BLOOD LEVEL; HUMAN; HUMAN CELL; HYPERAMMONEMIA; HYPOGLYCEMIA; INSULINOMA; MALE; METABOLIC DISORDER; OLIVOPONTOCEREBELLAR ATROPHY; PRIORITY JOURNAL; REVIEW; SEIZURE;

ACETYLTRANSFERASES; AMINO-ACID N-ACETYLTRANSFERASE; ATP-BINDING CASSETTE TRANSPORTERS; BACTERIAL PROTEINS; BRAIN DISEASES, METABOLIC; CHROMOSOMES, HUMAN, PAIR 10; EXONS; FEMALE; GENE EXPRESSION; GLUTAMATE DEHYDROGENASE; GLUTAMIC ACID; HUMANS; HYPERAMMONEMIA; HYPOGLYCEMIA; INFANT; LIVER; MALE; NITROGEN; POINT MUTATION; PYRIDOXINE; SEIZURES; UREA; X CHROMOSOME;

EID: 0035192281     PISSN: 10804013     EISSN: None     Source Type: Journal    
DOI: 10.1002/mrdd.1040     Document Type: Review

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