Literature DB >> 4100900

Hepatic delta-aminolaevulinic acid synthetase in an attack of hereditary coproporphyria and during remission.

N McIntyre, A J Pearson, D J Allan, S Craske, G M West, M R Moore, A D Beattie, J Paxton, A Goldberg.   

Abstract

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Year:  1971        PMID： 4100900     DOI： 10.1016/s0140-6736(71)91161-5

Source DB:  PubMed          Journal:  Lancet        ISSN： 0140-6736            Impact factor:   79.321


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  7 in total

Review 1.  The porphyrias: a review.

Authors:  G H Elder; C H Gray; D C Nicholson
Journal:  J Clin Pathol       Date:  1972-12       Impact factor: 3.411

2.  Hereditary coproporphyria and epilepsy.

Authors:  A B Houston; M J Brodie; M R Moore; G G Thompson; J B Stephenson
Journal:  Arch Dis Child       Date:  1977-08       Impact factor: 3.791

3.  Delta-Aminolaevulinic acid and amino acid neurotransmitters.

Authors:  M J Brennan; R C Cantrill
Journal:  Mol Cell Biochem       Date:  1981-08-11       Impact factor: 3.396

4.  Decreased red cell uroporphyrinogen I synthetase activity in intermittent acute porphyria.

Authors:  L J Strand; U A Meyer; B F Felsher; A G Redeker; H S Marver
Journal:  J Clin Invest       Date:  1972-10       Impact factor: 14.808

Review 5.  Free radicals involvement in neurological porphyrias and lead poisoning.

Authors:  H P Monteiro; E J Bechara; D S Abdalla
Journal:  Mol Cell Biochem       Date:  1991-04-24       Impact factor: 3.396

6.  Heme synthetase deficiency in human protoporphyria. Demonstration of the defect in liver and cultured skin fibroblasts.

Authors:  H L Bonkowsky; J R Bloomer; P S Ebert; M J Mahoney
Journal:  J Clin Invest       Date:  1975-11       Impact factor: 14.808

7.  Deficiency of hepatic coproporphyrinogen oxidase in hereditary coproporphyria.

Authors:  J L Hawk; I A Magnus; A Parkes; G H Elder; M Doyle
Journal:  J R Soc Med       Date:  1978-10       Impact factor: 18.000
  7 in total

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