Literature DB >> 7807934

Secondary 3-hydroxydicarboxylic aciduria mimicking long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency.

M J Bennett1, M J Weinberger, W G Sherwood, A B Burlina.   

Abstract

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Year:  1994        PMID： 7807934     DOI： 10.1007/BF00711808

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


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  11 in total

1.  Long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency: identification of a new inborn error of mitochondrial fatty acid beta-oxidation.

Authors:  R J Wanders; L IJlst; A H van Gennip; C Jakobs; J P de Jager; L Dorland; F J van Sprang; M Duran
Journal:  J Inherit Metab Dis       Date:  1990       Impact factor: 4.982

2.  A comparison of [9,10-3H]palmitic and [9,10-3H]myristic acids for the detection of defects of fatty acid oxidation in intact cultured fibroblasts.

Authors:  N J Manning; S E Olpin; R J Pollitt; J Webley
Journal:  J Inherit Metab Dis       Date:  1990       Impact factor: 4.982

3.  Sudden infant death and long-chain 3-hydroxyacyl-CoA dehydrogenase.

Authors:  R J Wanders; M Duran; L Ijlst; J P de Jager; A H van Gennip; C Jakobs; L Dorland; F J van Sprang
Journal:  Lancet       Date:  1989-07-01       Impact factor: 79.321

4.  Clinical and biochemical presentations in 20 cases of hydroxydicarboxylic aciduria.

Authors:  R J Pollitt
Journal:  Prog Clin Biol Res       Date:  1990

5.  The L-3-hydroxyacyl-CoA dehydrogenase deficiency.

Authors:  D E Hale; C Thorpe; K Braat; J H Wright; C R Roe; P M Coates; T Hashimoto; A M Glasgow
Journal:  Prog Clin Biol Res       Date:  1990

6.  Ethylmalonic aciduria associated with progressive neurological disease and partial cytochrome c oxidase deficiency.

Authors:  W Lehnert; W Ruitenbeek
Journal:  J Inherit Metab Dis       Date:  1993       Impact factor: 4.982

7.  Muscle cytochrome c oxidase deficiency accompanied by a urinary organic acid pattern mimicking multiple acyl-CoA dehydrogenase deficiency.

Authors:  E Christensen; N J Brandt; H Schmalbruch; Z Kamieniecka; B Hertz; W Ruitenbeek
Journal:  J Inherit Metab Dis       Date:  1993       Impact factor: 4.982

8.  Secondary inhibition of multiple NAD-requiring dehydrogenases in respiratory chain complex I deficiency: possible metabolic markers for the primary defect.

Authors:  M J Bennett; W G Sherwood; K M Gibson; A B Burlina
Journal:  J Inherit Metab Dis       Date:  1993       Impact factor: 4.982

9.  Human liver long-chain 3-hydroxyacyl-coenzyme A dehydrogenase is a multifunctional membrane-bound beta-oxidation enzyme of mitochondria.

Authors:  K Carpenter; R J Pollitt; B Middleton
Journal:  Biochem Biophys Res Commun       Date:  1992-03-16       Impact factor: 3.575

10.  Marked elevation of urinary 3-hydroxydecanedioic acid in a malnourished infant with glycogen storage disease, mimicking long-chain L-3-hydroxyacyl-CoA dehydrogenase deficiency.

Authors:  J Bergoffen; P Kaplan; D E Hale; M J Bennett; G T Berry
Journal:  J Inherit Metab Dis       Date:  1993       Impact factor: 4.982
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  12 in total

1.  Organic acid profiles resembling a beta-oxidation defect in two patients with coeliac disease.

Authors:  C G Costa; N M Verhoeven; C M Kneepkens; A C Douwes; R J Wanders; I T de Almeida; M Duran; C Jakobs
Journal:  J Inherit Metab Dis       Date:  1996       Impact factor: 4.982

Review 2.  Compromised fatty acid oxidation in mitochondrial disorders.

Authors:  L Hagenfeldt
Journal:  J Inherit Metab Dis       Date:  1998-08       Impact factor: 4.982

3.  Hypoketonuric 3-hydroxydicarboxylic aciduria in five patients with glycogen storage disease.

Authors:  C E Mize; L J Waber; T Anderson; M J Bennett
Journal:  J Inherit Metab Dis       Date:  1997-07       Impact factor: 4.982

4.  Mitochondropathy presenting with non-ketotic hypoglycaemia as 3-hydroxydicarboxylic aciduria.

Authors:  E Mayatepek; R J Wanders; M Becker; H J Bremer; G F Hoffmann
Journal:  J Inherit Metab Dis       Date:  1995       Impact factor: 4.982

5.  Do criteria exist from urinary organic acids to distinguish beta-oxidation defects?

Authors:  D Rabier; J Bardet; P Parvy; F Poggi; M Brivet; J M Saudubray; P Kamoun
Journal:  J Inherit Metab Dis       Date:  1995       Impact factor: 4.982

6.  Analysis of 3-hydroxydodecanedioic acid for studies of fatty acid metabolic disorders: preparation of stable isotope standards.

Authors:  J S Chickos; Barbara A Way; J Wilson; M Shaharuzzaman; J Laird; M Landt
Journal:  J Clin Lab Anal       Date:  2002       Impact factor: 2.352

7.  Evidence for physical association of mitochondrial fatty acid oxidation and oxidative phosphorylation complexes.

Authors:  Yudong Wang; Al-Walid Mohsen; Stephanie J Mihalik; Eric S Goetzman; Jerry Vockley
Journal:  J Biol Chem       Date:  2010-07-27       Impact factor: 5.157

8.  Fatty acid oxidation in fibroblasts from patients with defects in beta-oxidation and in the respiratory chain.

Authors:  N Venizelos; U von Döbeln; L Hagenfeldt
Journal:  J Inherit Metab Dis       Date:  1998-06       Impact factor: 4.982

Review 9.  Metabolism as a complex genetic trait, a systems biology approach: implications for inborn errors of metabolism and clinical diseases.

Authors:  Jerry Vockley
Journal:  J Inherit Metab Dis       Date:  2008-10-05       Impact factor: 4.982

Review 10.  Disorders of mitochondrial long-chain fatty acid oxidation.

Authors:  R J Pollitt
Journal:  J Inherit Metab Dis       Date:  1995       Impact factor: 4.982
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