Literature DB >> 6120052

Reduced ornithine catabolism in cultured fibroblasts and phytohaemagglutinin-stimulated lymphocytes from a patient with hyperornithinaemia, hyperammonaemia and homocitrullinuria.

R G Gray, S E Hill, R J Pollitt.   

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Year:  1982        PMID: 6120052     DOI: 10.1016/0009-8981(82)90001-8

Source DB:  PubMed          Journal:  Clin Chim Acta        ISSN: 0009-8981            Impact factor:   3.786


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  5 in total

1.  A new patient with hyperornithinaemia, hyperammonaemia and homocitrullinuria treated early with low protein diet.

Authors:  L R Gjessing; H A Lunde; T Undrum; H Broch; A Alme; S O Lie
Journal:  J Inherit Metab Dis       Date:  1986       Impact factor: 4.982

2.  Studies on the pathway from ornithine to proline in cultured skin fibroblasts with reference to the defect in hyperornithinaemia with hyperammonaemia and homocitrullinuria.

Authors:  R G Gray; S E Hill; R J Pollitt
Journal:  J Inherit Metab Dis       Date:  1983       Impact factor: 4.982

3.  A new family affected by the syndrome of hyperornithinaemia, hyperammonaemia and homocitrullinuria.

Authors:  M Rodes; A Ribes; M Pineda; L Alvarez; I Fabregas; E Fernandez Alvarez; F X Coude; G Grimber
Journal:  J Inherit Metab Dis       Date:  1987       Impact factor: 4.982

4.  The pH of mitochondria of fibroblasts from a hyperornithinaemia, hyperammonaemia, homocitrullinuria-syndrome patient.

Authors:  K Metoki; F A Hommes
Journal:  J Inherit Metab Dis       Date:  1984       Impact factor: 4.982

5.  Ultrastructural changes in fibroblast mitochondria of a patient with HHH-syndrome.

Authors:  K Metoki; F A Hommes; P Dyken; C Kelloes; J Trefz
Journal:  J Inherit Metab Dis       Date:  1984       Impact factor: 4.982

  5 in total

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