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24. A retrospective study of a patient with homozygous form of acute intermittent porphyria. Beukeveld GJ; Wolthers BG; Nordmann Y; Deybach JC; Grandchamp B; Wadman SK J Inherit Metab Dis; 1990; 13(5):673-83. PubMed ID: 2246851 [TBL] [Abstract][Full Text] [Related]
25. [Porphyrin-synthesizing enzymes in erythrocyte]. Kondo M Nihon Rinsho; 1995 Jun; 53(6):1371-6. PubMed ID: 7616649 [TBL] [Abstract][Full Text] [Related]
26. [Acute intermittent porphyria: uroporphyrinogen-I-synthetase activity in erythrocytes as a diagnostic index]. Formgren B; Wetterberg L Lakartidningen; 1978 May; 75(19):1921-4. PubMed ID: 651454 [No Abstract] [Full Text] [Related]
28. Determination of erythrocyte hydroxymethylbilane synthase activity and its application for study of acute intermittent porphyria. Lee FY; Hsiao KJ; Tsai YT; Lee SD; Wu SJ; Jeng HS Taiwan Yi Xue Hui Za Zhi; 1988 Nov; 87(11):1029-35. PubMed ID: 3235962 [No Abstract] [Full Text] [Related]
33. Homozygous acute intermittent porphyria in a 7-year-old boy with massive excretions of porphyrins and porphyrin precursors. Hessels J; Voortman G; van der Wagen A; van der Elzen C; Scheffer H; Zuijderhoudt FM J Inherit Metab Dis; 2004; 27(1):19-27. PubMed ID: 14970743 [TBL] [Abstract][Full Text] [Related]
34. Studies in porphyria. V. Drug oxidation rates in hereditary hepatic porphyria. Anderson KE; Alvares AP; Sassa S; Kappas A Clin Pharmacol Ther; 1976 Jan; 19(1):47-54. PubMed ID: 1245093 [TBL] [Abstract][Full Text] [Related]
35. An acute attack of variegate porphyria complicated by severe autonomic neuropathy. Stewart PM; Hensley WJ Aust N Z J Med; 1981 Feb; 11(1):82-3. PubMed ID: 6941785 [TBL] [Abstract][Full Text] [Related]
36. Studies in porphyria. IV. Expression of the gene defect of acute intermittent porphyria in cultured human skin fibroblasts and amniotic cells: prenatal diagnosis of the porphyric trait. Sassa S; Solish G; Levere RD; Kappas A J Exp Med; 1975 Sep; 142(3):722-31. PubMed ID: 1165472 [TBL] [Abstract][Full Text] [Related]