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5. The activities of the enzymes of haem biosynthesis in the porphyrias and during treatment of acute intermittent porphyrias. Moore MR; McColl KE; Goldberg A Int J Biochem; 1980; 12(5-6):941-6. PubMed ID: 7450153 [No Abstract] [Full Text] [Related]
6. Dual porphyria in double heterozygotes with porphobilinogen deaminase and uroporphyrinogen decarboxylase deficiencies. Doss MO Clin Genet; 1989 Feb; 35(2):146-51. PubMed ID: 2721023 [TBL] [Abstract][Full Text] [Related]
7. Is porphobilinogen deaminase activity a secondary control mechanism in haem biosynthesis in humans? [proceedings]. Brodie MJ; Moore MR; Thompson GG; Campbell BC; Goldberg A Biochem Soc Trans; 1977; 5(5):1466-8. PubMed ID: 923960 [No Abstract] [Full Text] [Related]
8. Genetic regulation of the red cell uroporphyrinogen-I-synthetase level in families with acute intermittent porphyria. Wetterberg L; Floderus Y; Thunell S; Iselius L; Lindsten J Clin Genet; 1983 Dec; 24(6):403-6. PubMed ID: 6652953 [TBL] [Abstract][Full Text] [Related]
9. Acute intermittent porphyria in The Netherlands. Heterogeneity of the enzyme porphobilinogen deaminase. Wilson JH; De Rooy FW; Te Velde K Neth J Med; 1986; 29(11):393-9. PubMed ID: 3808142 [No Abstract] [Full Text] [Related]
10. Haem biosynthesis in cutaneous hepatic porphyria: comparison with alcoholism and liver disease. Brodie MJ; Thompson GG; Moore MR; McColl KE; Goldberg A; Hardie RA; Hunter JA Acta Hepatogastroenterol (Stuttg); 1979 Apr; 26(2):122-8. PubMed ID: 463487 [TBL] [Abstract][Full Text] [Related]
11. Drug sensitivity in hereditary hepatic porphyria. Meyer UA Hum Genet Suppl; 1978; (1):71-8. PubMed ID: 285036 [No Abstract] [Full Text] [Related]
12. The treatment of acute intermittent porphyria with laevulose. Brodie MJ; Moore MR; Thompson GG; Goldberg A Clin Sci Mol Med; 1977 Oct; 53(4):365-71. PubMed ID: 913061 [TBL] [Abstract][Full Text] [Related]
13. Cloning of the Escherichia coli K-12 hemB gene. Li JM; Umanoff H; Proenca R; Russell CS; Cosloy SD J Bacteriol; 1988 Feb; 170(2):1021-5. PubMed ID: 3276659 [TBL] [Abstract][Full Text] [Related]
14. Relationships between acute hepatic porphyrias due to genetic variability of primary enzyme defects and limiting function of uroporphyrinogen synthase. Doss M Int J Biochem; 1978; 9(12):911-6. PubMed ID: 744295 [No Abstract] [Full Text] [Related]