Literature DB >> 4721588

[Constitutional hyperammonemia with carbamoylphosphate synthetase deficiency. Course treatment during dietetic].

M Odievre, C Charpentier, L Cathelineau, J Vedrenne, F Delacoux des Roseaux, C Mercie.   

Abstract

Entities:  

Mesh：

Substances：

Year:  1973        PMID： 4721588

Source DB:  PubMed          Journal:  Arch Fr Pediatr        ISSN： 0003-9764


× No keyword cloud information.
  3 in total

1.  Neonatal hyperammonaemia with complete absence of liver carbamyl phosphate synthetase activity.

Authors:  S Mantagos; S Tsagaraki; E A Burgess; V Oberholzer; T Palmer; J Sacks; S Baibas; T Valaes
Journal:  Arch Dis Child       Date:  1978-03       Impact factor: 3.791

2.  Carbamyl phosphate synthetase deficiency with lethal neonatal outcome.

Authors:  J Jaeken; H Devlieger; C Bachmann; J Van Aerde; L Corbeel; E Eggermont
Journal:  Eur J Pediatr       Date:  1982-09       Impact factor: 3.183

3.  Autosomal recessive inheritance of human mitochondrial carbamyl phosphate synthetase deficiency.

Authors:  J W McReynolds; B Crowley; M J Mahoney; L E Rosenberg
Journal:  Am J Hum Genet       Date:  1981-05       Impact factor: 11.025
  3 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.