Case Reports
Severe neonatal deficiency of carbamylphosphate synthetase
- PMID: 204150
Item in Clipboard
Case Reports
Severe neonatal deficiency of carbamylphosphate synthetase
Acta Paediatr Belg.
1977 Jul-Sep.
No abstract available
Similar articles
-
Carbamylphosphate synthetase-I deficiency in a newborn: survival after early diagnosis and therapy.Indian Pediatr. 1991 May;28(5):551-4. Indian Pediatr. 1991. PMID: 1752685 No abstract available.
-
[Comments on the contribution, Therapy of hyperammonemia in carbamylphosphate synthetase deficiency with peritoneal dialysis and venovenous hemofiltration, by B. Lettgen et al].Monatsschr Kinderheilkd. 1992 Jul;140(7):431. Monatsschr Kinderheilkd. 1992. PMID: 1308100 German. No abstract available.
-
[Therapy of hyperammonemia in carbamyl phosphate synthase deficiency with peritoneal dialysis and venovenous hemofiltration].Monatsschr Kinderheilkd. 1991 Sep;139(9):612-7. Monatsschr Kinderheilkd. 1991. PMID: 1745252 German.
-
[Carbamyl phosphate synthetase I deficiency].Ryoikibetsu Shokogun Shirizu. 1998;(18 Pt 1):167-9. Ryoikibetsu Shokogun Shirizu. 1998. PMID: 9590018 Review. Japanese. No abstract available.
-
[Hyperammonemias of childhood. I. Enzymopathies of the urea cycle].Pediatr Pol. 1987 Oct;62(10):727-32. Pediatr Pol. 1987. PMID: 3328149 Review. Polish. No abstract available.
Cited by
-
Carbamyl phosphate synthetase deficiency with lethal neonatal outcome.Eur J Pediatr. 1982 Sep;139(1):72-5. doi: 10.1007/BF00442085. Eur J Pediatr. 1982. PMID: 7173263 No abstract available.
-
Autosomal recessive inheritance of human mitochondrial carbamyl phosphate synthetase deficiency.Am J Hum Genet. 1981 May;33(3):345-53. Am J Hum Genet. 1981. PMID: 7246541 Free PMC article.