Literature DB >> 117250

Secondary metabolic changes in fibroblasts from six patients with hereditary lactic acidosis.

O Borud, J H Strømme.   

Abstract

Studies on fibroblasts from patients with lactic acidosis of different causes showed secondary metabolic changes in pathways of glucose metabolism. These secondary changes may be important clues to the diagnosis of the many different types of hereditary lactic acidosis.

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Year:  1978        PMID： 117250     DOI： 10.1007/bf01805587

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


  3 in total

1.  Leigh's encephalomyelopathy in a patient with cytochrome c oxidase deficiency in muscle tissue.

Authors:  J L Willems; L A Monnens; J M Trijbels; J H Veerkamp; A E Meyer; K van Dam; U van Haelst
Journal:  Pediatrics       Date:  1977-12       Impact factor: 7.124

2.  Fatal lactic acidosis in a newborn attributable to a congenital defect of pyruvate dehydrogenase.

Authors:  J H Strömme; O Borud; P J Moe
Journal:  Pediatr Res       Date:  1976-01       Impact factor: 3.756

3.  Metabolic studies on normal and pyruvate dehydrogenase deficient cultured human fibroblasts.

Authors:  O Borud; J H Stroomme
Journal:  Scand J Clin Lab Invest       Date:  1977-09       Impact factor: 1.713
  3 in total

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