Literature DB >> 2116558

3-Methylglutaconic aciduria with persistent metabolic acidosis and 'uncoupling episodes'.

O N Elpeleg1, D Meiron, V Barash, Y Hurwitz, I Tal, N Amir.   

Abstract

Entities:  

Mesh：

Substances：

Year:  1990        PMID： 2116558     DOI： 10.1007/bf01799695

Source DB:  PubMed          Journal:  J Inherit Metab Dis        ISSN： 0141-8955            Impact factor:   4.982


× No keyword cloud information.
  2 in total

1.  A case of severe hypermetabolism of nonthyroid origin with a defect in the maintenance of mitochondrial respiratory control: a correlated clinical, biochemical, and morphological study.

Authors:  R LUFT; D IKKOS; G PALMIERI; L ERNSTER; B AFZELIUS
Journal:  J Clin Invest       Date:  1962-09       Impact factor: 14.808

2.  3-Methylglutaconic aciduria: a phenotype in which activity of 3-methylglutaconyl-coenzyme A hydratase is normal.

Authors:  K M Gibson; W L Nyhan; L Sweetman; K Narisawa; W Lehnert; P Divry; B H Robinson; K S Roth; F A Beemer; F J van Sprang
Journal:  Eur J Pediatr       Date:  1988-10       Impact factor: 3.183
  2 in total
  2 in total

1.  3-Methylglutaconyl-coenzyme-A hydratase deficiency: a new case.

Authors:  K M Gibson; C F Lee; R S Wappner
Journal:  J Inherit Metab Dis       Date:  1992       Impact factor: 4.982

2.  Dilated cardiomyopathy with 3-methylglutaconic aciduria.

Authors:  J M Draaisma; I C van Kesteren; O Daniëls; R C Sengers
Journal:  Pediatr Cardiol       Date:  1994 Mar-Apr       Impact factor: 1.655
  2 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.