Literature DB >> 712737

Deficiency of hepatic coproporphyrinogen oxidase in hereditary coproporphyria.

J L Hawk, I A Magnus, A Parkes, G H Elder, M Doyle.   

Abstract

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Year:  1978        PMID： 712737      PMCID： PMC1436210          DOI： 10.1177/014107687807101018

Source DB:  PubMed          Journal:  J R Soc Med        ISSN： 0141-0768            Impact factor:   18.000


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  10 in total

1.  Hereditary coproporphyria.

Authors:  H BERGER; A GOLDBERG
Journal:  Br Med J       Date:  1955-07-09

2.  STUDIES OF COPROPORPHYRIN. III. IDIOPATHIC COPROPORPHYRINURIA; A HITHERTO UNRECOGNIZED FORM CHARACTERIZED BY LACK OF SYMPTOMS IN SPITE OF THE EXCRETION OF LARGE AMOUNTS OF COPROPORPHYRIN.

Authors:  C J Watson; S Schwartz; W Schulze; L O Jacobson; R Zagaria
Journal:  J Clin Invest       Date:  1949-05       Impact factor: 14.808

3.  Hereditary coproporphyria presenting with photosensitivity induced by the contraceptive pill.

Authors:  D T Roberts; M J Brodie; M R Moore; G G Thompson; A Goldberg; R N MacSween
Journal:  Br J Dermatol       Date:  1977-05       Impact factor: 9.302

4.  Hereditary coproporphyria. Demonstration of the abnormalities in haem biosynthesis in peripheral blood.

Authors:  M J Brodie; G G Thompson; M R Moore; A D Beattie; A Goldberg
Journal:  Q J Med       Date:  1977-04

5.  Hereditary coproporphyria.

Authors:  A Goldberg; C Rimington; A C Lochhead
Journal:  Lancet       Date:  1967-03-25       Impact factor: 79.321

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

Authors:  N McIntyre; A J Pearson; D J Allan; S Craske; G M West; M R Moore; A D Beattie; J Paxton; A Goldberg
Journal:  Lancet       Date:  1971-03-20       Impact factor: 79.321

7.  Biochemical defects in two types of human hepatic porphyria.

Authors:  L Kaufman; H S Marver
Journal:  N Engl J Med       Date:  1970-10-29       Impact factor: 91.245

8.  Decreased lymphocyte coproporphyrinogen III oxidase activity in hereditary coproporphyria.

Authors:  B Grandchamp; Y Nordmann
Journal:  Biochem Biophys Res Commun       Date:  1977-02-07       Impact factor: 3.575

9.  The primary enzyme defect in hereditary coproporphyria.

Authors:  G H Elder; J O Evans; N Thomas
Journal:  Lancet       Date:  1976-12-04       Impact factor: 79.321

10.  A radiochemical method for the measurement of coproporphyrinogen oxidase and the utilization of substrates other than coproporphyrinogen III by the enzyme from rat liver.

Authors:  G H Elder; J O Evans
Journal:  Biochem J       Date:  1978-01-01       Impact factor: 3.857
  10 in total
  1 in total

1.  Characterization of mutations in the CPO gene in British patients demonstrates absence of genotype-phenotype correlation and identifies relationship between hereditary coproporphyria and harderoporphyria.

Authors:  J Lamoril; H Puy; S D Whatley; C Martin; J R Woolf; V Da Silva; J C Deybach; G H Elder
Journal:  Am J Hum Genet       Date:  2001-04-16       Impact factor: 11.025
  1 in total

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