Treatment of urea cycle disorders

Journal of Pediatrics

Volumn 134, Issue 3, 1999, Pages 255-256

  Thoene, J G ^a  

^a UNIVERSITY OF MICHIGAN MEDICAL SCHOOL   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ARGININE; ARYLBUTYRIC ACID DERIVATIVE; BENZOIC ACID DERIVATIVE; CITRULLINE; ORNITHINE CARBAMOYLTRANSFERASE; OXOACID; PHENYLACETIC ACID; UCEPHAN;

EDITORIAL; ENZYME DEFICIENCY; GENE THERAPY; HUMAN; LIVER TRANSPLANTATION; METABOLIC DISORDER; PRIORITY JOURNAL; RESPIRATORY ALKALOSIS;

EID: 0033506342     PISSN: 00223476     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0022-3476(99)70443-9     Document Type: Editorial

References (8)

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3. RG Westall Argininosuccinic aciduria: identification and reactions of the abnormal metabolites in a newly described form of mental disease, with some preliminary metabolic studies Biochem J 77 1960 135 144
4. J Thoene M Batshaw E Spector S Kulovich S Brusilow M Walser Neonatal citrullinemia: treatment with keto-analogues of essential amino acids J Pediatr 90 1977 218 224
5. M Batshaw S Brusilow M Walser Treatment of carbamyl phosphate synthetase deficiency with keto-analogues of essential amino acids N Engl J Med 292 1975 1085 1090
6. NE Maestri D Clissold SW Brusilow Neonatal onset ornithine transcarbamylase deficiency: a retrospective analysis J Pediatr 134 1999 268 272
7. J Thoene Inborn errors of metabolism 2nd ed J Thoene Physicians guide to rare diseases 1995 Dowden Publishing Montvale (NJ) 167 171
8. X Ye MB Robinson ML Batshaw EE Furth I Smith JM Wilson Prolonged metabolic correction in adult ornithine transcarbamylase-deficient mice with adenoviral vectors J Biol Chem 271 1996 3639 3646