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24. Enzyme defects in hereditary porphyria. Civin WH; Epstein E Ann Clin Lab Sci; 1980; 10(5):395-401. PubMed ID: 6999973 [TBL] [Abstract][Full Text] [Related]
25. [Hereditary uroporphyrinogen decarboxylase deficiency in porphyria cutanea tarda caused by hormonal contraceptives]. Doss M Dtsch Med Wochenschr; 1983 Dec; 108(48):1857-8. PubMed ID: 6641540 [No Abstract] [Full Text] [Related]
26. Erythrocyte uroporphyrinogen decarboxylase activity in porphyria cutanea tarda: a study of 40 consecutive patients. Held JL; Sassa S; Kappas A; Harber LC J Invest Dermatol; 1989 Sep; 93(3):332-4. PubMed ID: 2768832 [TBL] [Abstract][Full Text] [Related]
27. Activation of uroporphyrinogen decarboxylase by ferrous iron in porphyria cutanea tarda. Blekkenhorst GH; Eales L; Pimstone NR S Afr Med J; 1979 Nov; 56(22):918-20. PubMed ID: 515872 [TBL] [Abstract][Full Text] [Related]
28. Familial porphyria cutanea tarda with normal erythrocytic urodecarboxylase: an exception to the rule? D'Alessandro Gandolfo L; Griso D; Macri A; Biolcati G; Topi GC Dermatologica; 1989; 178(4):206-8. PubMed ID: 2767288 [TBL] [Abstract][Full Text] [Related]
29. [Uroporphyrinogen decarboxylase in erythrocytes: studies on the primary genetic enzyme defect in chronic hepatic porphyria (author's transl)]. von Tiepermann R; Doss M J Clin Chem Clin Biochem; 1978 Sep; 16(9):513-7. PubMed ID: 712342 [TBL] [Abstract][Full Text] [Related]
31. Reduced substrate affinity for human erythrocyte uroporphyrinogen decarboxylase constitutes the inherent biochemical defect in porphyria cutanea tarda. Mukerji SK; Pimstone NR Biochem Biophys Res Commun; 1985 Mar; 127(2):517-25. PubMed ID: 3977935 [TBL] [Abstract][Full Text] [Related]
32. Dual mechanism of inhibition of rat liver uroporphyrinogen decarboxylase activity by ferrous iron: its potential role in the genesis of porphyria cutanea tarda. Mukerji SK; Pimstone NR; Burns M Gastroenterology; 1984 Dec; 87(6):1248-54. PubMed ID: 6489695 [TBL] [Abstract][Full Text] [Related]
37. Uroporphyrinogen decarboxylase: a splice site mutation causes the deletion of exon 6 in multiple families with porphyria cutanea tarda. Garey JR; Harrison LM; Franklin KF; Metcalf KM; Radisky ES; Kushner JP J Clin Invest; 1990 Nov; 86(5):1416-22. PubMed ID: 2243121 [TBL] [Abstract][Full Text] [Related]
38. [Hepato-erythrocytic porphyria in 2 female twins]. Sfar Z; Kamoun MR; Kastally R; De Verneuil H; Nordmann Y Ann Dermatol Venereol; 1985; 112(5):453-6. PubMed ID: 4041155 [No Abstract] [Full Text] [Related]
39. Uroporphyrinogen decarboxylase structural mutant (Gly281----Glu) in a case of porphyria. de Verneuil H; Grandchamp B; Beaumont C; Picat C; Nordmann Y Science; 1986 Nov; 234(4777):732-4. PubMed ID: 3775362 [TBL] [Abstract][Full Text] [Related]
40. Defective human erythrocyte uroporphyrinogen decarboxylase in familial porphyria cutanea tarda: the metabolic lesion or the result of endogenous porphyrinemia? Mukerji SK; Pimstone NR Biochem Biophys Res Commun; 1988 Jul; 154(1):39-46. PubMed ID: 3395340 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]