Literature DB >> 7609452

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

M J Bennett1, W G Sherwood, K M Gibson, A B Burlina.   

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Year:  1993        PMID： 7609452     DOI： 10.1007/BF00711681

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


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  3 in total

1.  3-Methylglutaconic aciduria in a patient with a disturbed mitochondrial energy metabolism.

Authors:  J A Bakkeren; R C Sengers; W Ruitenbeek; J M Trijbels
Journal:  Eur J Pediatr       Date:  1992-04       Impact factor: 3.183

2.  Pearson's marrow-pancreas syndrome. A multisystem mitochondrial disorder in infancy.

Authors:  A Rötig; V Cormier; S Blanche; J P Bonnefont; F Ledeist; N Romero; J Schmitz; P Rustin; A Fischer; J M Saudubray
Journal:  J Clin Invest       Date:  1990-11       Impact factor: 14.808

3.  Organic acids in urine of patients with congenital lactic acidoses: an aid to differential diagnosis.

Authors:  R A Chalmers
Journal:  J Inherit Metab Dis       Date:  1984       Impact factor: 4.982
  3 in total
  8 in total

1.  Profound neurological phenotype in a patient presenting with disordered isoleucine and energy metabolism.

Authors:  A B Burlina; K M Gibson; W Ruitenbeek; L Bonafè; M J Bennett
Journal:  J Inherit Metab Dis       Date:  1998-12       Impact factor: 4.982

2.  3-Hydroxyisobutyrate aciduria and mutations in the ALDH6A1 gene coding for methylmalonate semialdehyde dehydrogenase.

Authors:  Jörn Oliver Sass; Melanie Walter; Julian P H Shield; Andrea M Atherton; Uttam Garg; David Scott; C Geoffrey Woods; Laurie D Smith
Journal:  J Inherit Metab Dis       Date:  2011-08-24       Impact factor: 4.982

3.  2-methyl-3-hydroxybutyryl-CoA dehydrogenase deficiency in a 23-year-old man.

Authors:  S E Olpin; R J Pollitt; J McMenamin; N J Manning; G Besley; J P N Ruiter; R J A Wanders
Journal:  J Inherit Metab Dis       Date:  2002-10       Impact factor: 4.982

4.  Respiratory complex II defect in siblings associated with a symptomatic secondary block in fatty acid oxidation.

Authors:  J J Gargus; K Boyle; M Bocian; D S Roe; C Vianey-Saban; C R Roe
Journal:  J Inherit Metab Dis       Date:  2003       Impact factor: 4.982

Review 5.  Mitochondrial disease in childhood: nuclear encoded.

Authors:  Amy C Goldstein; Poonam Bhatia; Jodie M Vento
Journal:  Neurotherapeutics       Date:  2013-04       Impact factor: 7.620

Review 6.  Disorders of mitochondrial long-chain fatty acid oxidation.

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

7.  In vivo isotope tracing reveals a requirement for the electron transport chain in glucose and glutamine metabolism by tumors.

Authors:  Panayotis Pachnis; Zheng Wu; Brandon Faubert; Alpaslan Tasdogan; Wen Gu; Spencer Shelton; Ashley Solmonson; Aparna D Rao; Akash K Kaushik; Thomas J Rogers; Jessalyn M Ubellacker; Collette A LaVigne; Chendong Yang; Bookyung Ko; Vijayashree Ramesh; Jessica Sudderth; Lauren G Zacharias; Misty S Martin-Sandoval; Duyen Do; Thomas P Mathews; Zhiyu Zhao; Prashant Mishra; Sean J Morrison; Ralph J DeBerardinis
Journal:  Sci Adv       Date:  2022-08-31       Impact factor: 14.957

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

Authors:  M J Bennett; M J Weinberger; W G Sherwood; A B Burlina
Journal:  J Inherit Metab Dis       Date:  1994       Impact factor: 4.982
  8 in total

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