A trial with N-carbamylglutamate may not detect all patients with NAGS deficiency and neonatal onset.

Journal of inherited metabolic disease

Volumn 30, Issue 3, 2007, Pages 400-

  Nordenstrom A ^a   Halldin, M ^a   Hallberg, B ^a   Alm, J ^a  

^a KAROLINSKA UNIVERSITY HOSPITAL   (Sweden)

Author keywords

[No Author keywords available]

Indexed keywords

AMINO ACID ACETYLTRANSFERASE; AMMONIA; UREA;

ARTICLE; BLOOD; CASE REPORT; DIFFERENTIAL DIAGNOSIS; DISORDERS OF AMINO ACID AND PROTEIN METABOLISM; HUMAN; METABOLISM; NEWBORN; TREATMENT OUTCOME;

AMINO ACID METABOLISM, INBORN ERRORS; AMINO-ACID N-ACETYLTRANSFERASE; AMMONIA; DIAGNOSIS, DIFFERENTIAL; HUMANS; INFANT, NEWBORN; TREATMENT OUTCOME; UREA;

EID: 34548022622     PISSN: None     EISSN: 15732665     Source Type: Journal    
DOI: 10.1007/s10545-007-0454-9     Document Type: Article

References (0)