Literature DB >> 518407

Hereditary hyperammonaemic syndromes--a six year experience.

E A Haan, D M Danks, N J Hoogenraad, J G Rogers.   

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Year:  1979        PMID： 518407     DOI： 10.1111/j.1440-1754.1979.tb01212.x

Source DB:  PubMed          Journal:  Aust Paediatr J        ISSN： 0004-993X


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  3 in total

1.  Glutamine-valine index - An aid in the detection of urea-cycle disorders.

Authors:  A Briddon; V G Oberholzer
Journal:  Amino Acids       Date:  1991-06       Impact factor: 3.520

2.  Immunological evidence for an ornithine transcarbamylase lesion resulting in the formation of enzyme with smaller protein subunits.

Authors:  N Hoogenraad; M Luisa de Martinis; D M Danks
Journal:  J Inherit Metab Dis       Date:  1983       Impact factor: 4.982

3.  Neurological features and computed tomography of the brain in children with ornithine carbamoyl transferase deficiency.

Authors:  B E Kendall; D P Kingsley; J V Leonard; S Lingam; V G Oberholzer
Journal:  J Neurol Neurosurg Psychiatry       Date:  1983-01       Impact factor: 10.154
  3 in total

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