Literature DB >> 8650841

Hereditary coproporphyria.

A Paterson1, D P Nicholls.   

Abstract

Mesh：

Year:  1994        PMID： 8650841      PMCID： PMC2448750     

Source DB:  PubMed          Journal:  Ulster Med J        ISSN： 0041-6193


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  5 in total

Review 1.  Biochemistry of porphyria.

Authors:  M R Moore
Journal:  Int J Biochem       Date:  1993-10

2.  "Glucose effect" and rate limiting function of uroporphyrinogen synthase on porphyrin metabolism in hepatocyte culture: relationship with human acute hepatic porphyrias.

Authors:  M Doss; F Sixel-Dietrich; F Verspohl
Journal:  J Clin Chem Clin Biochem       Date:  1985-09

Review 3.  The acute porphyrias.

Authors:  G Y Lip; K E McColl; M R Moore
Journal:  Br J Clin Pract       Date:  1993 Jan-Feb

4.  Tin protoporphyrin prolongs the biochemical remission produced by heme arginate in acute hepatic porphyria.

Authors:  S B Dover; M R Moore; E J Fitzsimmons; A Graham; K E McColl
Journal:  Gastroenterology       Date:  1993-08       Impact factor: 22.682

5.  Homozygous hereditary coproporphyria caused by an arginine to tryptophane substitution in coproporphyrinogen oxidase and common intragenic polymorphisms.

Authors:  P Martasek; Y Nordmann; B Grandchamp
Journal:  Hum Mol Genet       Date:  1994-03       Impact factor: 6.150
  5 in total

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