Vascular dysfunction as an additional pathomechanism in glutaric aciduria type I

Journal of Inherited Metabolic Disease

Volumn 27, Issue 6, 2004, Pages 829-834

  Muhlhausen C ^a   Ergun S ^a   Strauss, K A ^b   Koeller, D M ^c   Crnic, L ^d   Woontner, M ^d   Goodman, S I ^d   Ullrich, K ^a   Braulke, T ^a  

^a UNIVERSITY MEDICAL CENTER HAMBURG EPPENDORF   (Germany)

^b Metabolic Service   (United States)

^c OREGON HEALTH AND SCIENCE UNIVERSITY   (United States)

^d Children's Hospital Colorado   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

3 HYDROXYGLUTARIC ACID; GLUTARIC ACID; GLUTARIC ACID DERIVATIVE; GLUTARYL COENZYME A DEHYDROGENASE; UNCLASSIFIED DRUG;

ACIDURIA; ANGIOGENESIS; ANIMAL CELL; ANIMAL EXPERIMENT; ANIMAL MODEL; ANIMAL TISSUE; ARTICLE; BLOOD VESSEL PERMEABILITY; BRAIN ARACHNOID; BRAIN BLOOD VESSEL; CEREBROVASCULAR DISEASE; CLINICAL OBSERVATION; CONTROLLED STUDY; CORPUS STRIATUM; DNA MICROARRAY; ENZYME DEFICIENCY; GENE IDENTIFICATION; GLUTARIC ACIDURIA TYPE 1; HUMAN; IN VITRO STUDY; IN VIVO STUDY; MALE; MOUSE; NEUROTOXICITY; NONHUMAN; NUCLEAR MAGNETIC RESONANCE IMAGING; PATHOGENESIS; PATHOPHYSIOLOGY; PRENATAL DEVELOPMENT; SUBDURAL EFFUSION; VASCULAR ENDOTHELIUM;

AMINO ACID METABOLISM, INBORN ERRORS; ANIMALS; BRAIN DISEASES; CEREBROVASCULAR CIRCULATION; GLUTARATES; GLUTARYL-COA DEHYDROGENASE; HUMANS; OLIGONUCLEOTIDE ARRAY SEQUENCE ANALYSIS; OXIDOREDUCTASES ACTING ON CH-CH GROUP DONORS; VASCULAR DISEASES;

EID: 7244226304     PISSN: 01418955     EISSN: None     Source Type: Journal    
DOI: 10.1023/B:BOLI.0000045766.98718.d6     Document Type: Article

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