Literature DB >> 2512434

Generalised dicarboxylic aciduria: a common finding in neonates.

M Downing1, P Rose, M J Bennett, N J Manning, R J Pollitt.   

Abstract

Entities:  

Mesh：

Substances：

Year:  1989        PMID： 2512434     DOI： 10.1007/bf03335411

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


× No keyword cloud information.
  9 in total

1.  Urinary organic acids quantitated by age groups in a healthy pediatric population.

Authors:  J A Thompson; B S Miles; P V Fennessey
Journal:  Clin Chem       Date:  1977-09       Impact factor: 8.327

2.  Defects of metabolism of fatty acids in the sudden infant death syndrome.

Authors:  A J Howat; M J Bennett; S Variend; L Shaw; P C Engel
Journal:  Br Med J (Clin Res Ed)       Date:  1985-06-15

3.  Prenatal diagnosis of medium-chain acyl-CoA dehydrogenase deficiency in family with sudden infant death.

Authors:  M J Bennett; F Allison; R J Pollitt; N J Manning; R G Gray; A Green; D E Hale; P M Coates
Journal:  Lancet       Date:  1987-02-21       Impact factor: 79.321

4.  Sudden infant death and inherited disorders of fat oxidation.

Authors: 
Journal:  Lancet       Date:  1986-11-08       Impact factor: 79.321

5.  Concentrations of organic acids in the urine of healthy newborn children.

Authors:  J Alm; L Hagenfeldt; A Larsson
Journal:  Ann Clin Biochem       Date:  1978-09       Impact factor: 2.057

6.  Organic acids in urine from human newborns.

Authors:  L Björkman; C McLean; G Steen
Journal:  Clin Chem       Date:  1976-01       Impact factor: 8.327

7.  General (medium-chain) acyl-CoA dehydrogenase deficiency (non-ketotic dicarboxylic aciduria): quantitative urinary excretion pattern of 23 biologically significant organic acids in three cases.

Authors:  N Gregersen; S Kølvraa; K Rasmussen; P B Mortensen; P Divry; M David; N Hobolth
Journal:  Clin Chim Acta       Date:  1983-08-15       Impact factor: 3.786

8.  Low molecular weight organic acids in the urine of the newborn.

Authors:  N Gregersen; J Ingerslev; K Rasmussen
Journal:  Acta Paediatr Scand       Date:  1977-01

9.  Genetic deficiency of medium-chain acyl coenzyme A dehydrogenase: studies in cultured skin fibroblasts and peripheral mononuclear leukocytes.

Authors:  P M Coates; D E Hale; C A Stanley; B E Corkey; J A Cortner
Journal:  Pediatr Res       Date:  1985-07       Impact factor: 3.756
  9 in total
  3 in total

1.  Dicarboxylic aciduria, significance and prognostic indications.

Authors:  E Treacy; J Pitt; M Eggington; R Hawkins
Journal:  Eur J Pediatr       Date:  1994-12       Impact factor: 3.183

2.  Analysis of abnormal urinary metabolites in the newborn period in medium-chain acyl-CoA dehydrogenase deficiency.

Authors:  M J Bennett; P M Coates; D E Hale; D S Millington; R J Pollitt; P Rinaldo; C R Roe; K Tanaka
Journal:  J Inherit Metab Dis       Date:  1990       Impact factor: 4.982

Review 3.  Disorders of mitochondrial beta-oxidation: prenatal and early postnatal diagnosis and their relevance to Reye's syndrome and sudden infant death.

Authors:  R J Pollitt
Journal:  J Inherit Metab Dis       Date:  1989       Impact factor: 4.982
  3 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.