Glutaric aciduria type 1: Proton magnetic resonance spectroscopy findings

Pediatric Neurology

Volumn 31, Issue 3, 2004, Pages 228-231

  Kurul, Semra ^a   Çakmakçi, Handan ^b   Dirik, Eray ^a  

^a Department of Pediatric Neurology ^*

^b DOKUZ EYLUL UNIVERSITY   (Turkey)

Author keywords

[No Author keywords available]

Indexed keywords

CARNITINE; CHOLINE; CREATINE; GLUTARYL COENZYME A DEHYDROGENASE; INOSITOL; N ACETYLASPARTIC ACID; RIBOFLAVIN;

ANAMNESIS; ARTICLE; ASTROCYTOSIS; BRAIN INJURY; BRAIN TOMOGRAPHY; CASE REPORT; CHILD; CLINICAL FEATURE; COMPARATIVE STUDY; DEMYELINATING DISEASE; DIAGNOSTIC APPROACH ROUTE; DIAGNOSTIC IMAGING; DIAGNOSTIC TEST; DISEASE COURSE; ENZYME DEFICIENCY; FOLLOW UP; FRONTAL CORTEX; GENETIC ANALYSIS; GLUTARIC ACIDURIA TYPE 1; HUMAN; INBORN ERROR OF METABOLISM; LABORATORY TEST; MALE; MEDICAL ASSESSMENT; MEDICAL EXAMINATION; METABOLIC DISORDER; NEUROAXONAL DYSTROPHY; NUCLEAR MAGNETIC RESONANCE IMAGING; PRIORITY JOURNAL; PROTEIN RESTRICTION; PROTON NUCLEAR MAGNETIC RESONANCE; TREATMENT PLANNING; WHITE MATTER;

BRAIN DISEASES, METABOLIC, INBORN; GLUTARATES; GLUTARYL-COA DEHYDROGENASE; HUMANS; INFANT; MAGNETIC RESONANCE SPECTROSCOPY; MALE; OXIDOREDUCTASES ACTING ON CH-CH GROUP DONORS; PROTONS;

EID: 4544315182     PISSN: 08878994     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.pediatrneurol.2004.02.009     Document Type: Article

References (13)

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