Literature DB >> 619088

Propionic acidemia with severe hyperammonemia and defective glycine metabolism.

T Shafai, L Sweetman, W Weyler, S I Goodman, P V Fennessey, W L Nyhan.   

Abstract

Entities:  

Mesh：

Substances：

Year:  1978        PMID： 619088     DOI： 10.1016/s0022-3476(78)80081-x

Source DB:  PubMed          Journal:  J Pediatr        ISSN： 0022-3476            Impact factor:   4.406


× No keyword cloud information.
  4 in total

Review 1.  The biotin-dependent carboxylase deficiencies.

Authors:  B Wolf; G L Feldman
Journal:  Am J Hum Genet       Date:  1982-09       Impact factor: 11.025

2.  Effects of a single dose of N-carbamylglutamate on the rate of ureagenesis.

Authors:  Nicholas Ah Mew; Irma Payan; Yevgeny Daikhin; Ilana Nissim; Itzhak Nissim; Mendel Tuchman; Marc Yudkoff
Journal:  Mol Genet Metab       Date:  2009-07-14       Impact factor: 4.797

3.  Propionyl coenzyme A carboxylase deficiency presenting as non-ketotic hyperglycinaemia.

Authors:  D J Harris; R M Thompson; B Wolf; B I Yang
Journal:  J Med Genet       Date:  1981-04       Impact factor: 6.318

4.  Inhibition by propionyl-coenzyme A of N-acetylglutamate synthetase in rat liver mitochondria. A possible explanation for hyperammonemia in propionic and methylmalonic acidemia.

Authors:  F X Coude; L Sweetman; W L Nyhan
Journal:  J Clin Invest       Date:  1979-12       Impact factor: 14.808
  4 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.