Literature DB >> 221857

Friedreich ataxia. II. Normal kinetics of lipoamide dehydrogenase.

D A Stumpf, J K Parks.   

Abstract

Lipoamide dehydrogenase (LAD) kinetic values, Km and Vmax, were normal in 11 patients with Friedreich ataxia. Fibroblast activities of the pyruvate and alpha-ketoglutarate dehydrogenase complex, and LAD activities, were also normal. There was no reduction in oxidative decarboxylation of pyruvate, alpha-ketoglutarate, or several other substrates in intact fibroblasts. Methodologic differences may account for differences of opinion about putative abnormalities of the alpha-ketoacid dehydrogenase complexes.

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Year:  1979        PMID: 221857     DOI: 10.1212/wnl.29.6.820

Source DB:  PubMed          Journal:  Neurology        ISSN: 0028-3878            Impact factor:   9.910


  8 in total

1.  Biochemical study in 28 children with lactic acidosis, in relation to Leigh's encephalomyelopathy.

Authors:  S Miyabayashi; T Ito; K Narisawa; K Iinuma; K Tada
Journal:  Eur J Pediatr       Date:  1985-03       Impact factor: 3.183

2.  Long-term treatment with thiamine as possible medical therapy for Friedreich ataxia.

Authors:  Antonio Costantini; Tiziana Laureti; Maria Immacolata Pala; Marco Colangeli; Simona Cavalieri; Elisa Pozzi; Alfredo Brusco; Sandro Salvarani; Carlo Serrati; Roberto Fancellu
Journal:  J Neurol       Date:  2016-08-03       Impact factor: 4.849

3.  Mitochondrial malic enzyme in Friedreich's ataxia: failure to demonstrate reduced activity in cultured fibroblasts.

Authors:  R G Gray; D Kumar
Journal:  J Neurol Neurosurg Psychiatry       Date:  1985-01       Impact factor: 10.154

4.  Biochemical and clinical studies of Friedreich's ataxia.

Authors:  P Purkiss; M Baraitser; O Borud; R A Chalmers
Journal:  J Neurol Neurosurg Psychiatry       Date:  1981-07       Impact factor: 10.154

5.  Pyruvate-dehydrogenase complex in ataxic patients: enzyme deficiency in ataxic encephalopathy plus lactic acidosis and normal activity in Friedreich ataxia.

Authors:  G Uziel; E Bottacchi; G Moschen; P Giovanardi-Rossi; G Cardace; S Di Donato
Journal:  Ital J Neurol Sci       Date:  1982-12

6.  Detection of heterozygotes in maple-syrup-urine disease: measurements of branched-chain alpha-ketoacid dehydrogenase and its components in cell cultures.

Authors:  D T Chuang; L S Ku; D S Kerr; R P Cox
Journal:  Am J Hum Genet       Date:  1982-05       Impact factor: 11.025

7.  Glutamate dehydrogenase deficiency in spinocerebellar degenerations.

Authors:  T Yamaguchi; K Hayashi; H Murakami; K Ota; S Maruyama
Journal:  Neurochem Res       Date:  1982-05       Impact factor: 3.996

8.  Pyruvate dehydrogenase complex activity in normal and deficient fibroblasts.

Authors:  K F Sheu; C W Hu; M F Utter
Journal:  J Clin Invest       Date:  1981-05       Impact factor: 14.808

  8 in total

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