Literature DB >> 4140439

Letter: Metabolic defect in hyperornithinaemia.

V E Shih, R Mandell.   

Abstract

Entities:  

Mesh：

Substances：

Year:  1974        PMID： 4140439     DOI： 10.1016/s0140-6736(74)90267-0

Source DB:  PubMed          Journal:  Lancet        ISSN： 0140-6736            Impact factor:   79.321


× No keyword cloud information.
  3 in total

1.  Abnormality of citrulline synthesis in liver mitochondria from patients with hyperornithinaemia, hyperammonaemia and homocitrullinuria.

Authors:  I Inoue; M Koura; T Saheki; K Kayanuma; M Uono; M Nakajima; K Takeshita; R Koike; T Yuasa; T Miyatake
Journal:  J Inherit Metab Dis       Date:  1987       Impact factor: 4.982

2.  Defective ornithine metabolism in the syndrome of hyperornithinaemia, hyperammonaemia and homocitrullinuria.

Authors:  V E Shih; R Mandell; A Herzfeld
Journal:  J Inherit Metab Dis       Date:  1981       Impact factor: 4.982

Review 3.  The hyperornithinemia-hyperammonemia-homocitrullinuria syndrome.

Authors:  Diego Martinelli; Daria Diodato; Emanuela Ponzi; Magnus Monné; Sara Boenzi; Enrico Bertini; Giuseppe Fiermonte; Carlo Dionisi-Vici
Journal:  Orphanet J Rare Dis       Date:  2015-03-11       Impact factor: 4.123
  3 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.