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2. Hereditary coproporphyria in Germany: clinical-biochemical studies in 53 patients. Kühnel A; Gross U; Doss MO Clin Biochem; 2000 Aug; 33(6):465-73. PubMed ID: 11074238 [TBL] [Abstract][Full Text] [Related]
3. Studies on coproporphyrin isomers in urine and feces in the porphyrias. Kühnel A; Gross U; Jacob K; Doss MO Clin Chim Acta; 1999 Apr; 282(1-2):45-58. PubMed ID: 10340433 [TBL] [Abstract][Full Text] [Related]
10. Hereditary coproporphyria. Demonstration of the abnormalities in haem biosynthesis in peripheral blood. Brodie MJ; Thompson GG; Moore MR; Beattie AD; Goldberg A Q J Med; 1977 Apr; 46(182):229-41. PubMed ID: 866576 [TBL] [Abstract][Full Text] [Related]
11. A molecular, enzymatic and clinical study in a family with hereditary coproporphyria. Gross U; Puy H; Meissauer U; Lamoril J; Deybach JC; Doss M; Nordmann Y; Doss MO J Inherit Metab Dis; 2002 Aug; 25(4):279-86. PubMed ID: 12227458 [TBL] [Abstract][Full Text] [Related]
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13. [Demonstration of hereditary enzyme defect in coproporphyria]. Grandchamp B; Phung N; Grelier M; de Verneuil H; Noiré J; Ohnet JP; Nordmann Y Nouv Presse Med; 1977 Apr; 6(18):1537-9. PubMed ID: 866144 [TBL] [Abstract][Full Text] [Related]
14. Hereditary coproporphyria: demonstration of a genetic defect in coproporphyrinogen metabolism. Nordmann Y; Grandchamp B Monogr Hum Genet; 1978; 10():217-22. PubMed ID: 723897 [No Abstract] [Full Text] [Related]
15. Biochemical and genetic characterization of four cases of hereditary coproporphyria in Spain. To-Figueras J; Badenas C; Enríquez MT; Segura S; Alvarez C; Milà M; Lecha M; Herrero C Mol Genet Metab; 2005 Jun; 85(2):160-3. PubMed ID: 15896662 [TBL] [Abstract][Full Text] [Related]
16. Precision and accuracy of a HPLC method for measurement of fecal porphyrin concentrations. Zuijderhoudt FM; Kamphuis JS; Kluitenberg WE; Dorresteijn-de Bok J Clin Chem Lab Med; 2002 Oct; 40(10):1036-9. PubMed ID: 12476945 [TBL] [Abstract][Full Text] [Related]
17. Quantitative fluorometric screening test for fecal porphyrins. Pudek MR; Schreiber WE; Jamani A Clin Chem; 1991 Jun; 37(6):826-31. PubMed ID: 2049846 [TBL] [Abstract][Full Text] [Related]
18. Family study of acute intermittent porphyria and hereditary coproporphyria in Niigata and Akita Prefectures, Japan. Sasaki H; Kaneko K; Tsuneyama H; Daimon M; Yamatani K; Manaka H J Clin Epidemiol; 1996 Oct; 49(10):1117-23. PubMed ID: 8826991 [TBL] [Abstract][Full Text] [Related]
20. Characterization of mutations in the CPO gene in British patients demonstrates absence of genotype-phenotype correlation and identifies relationship between hereditary coproporphyria and harderoporphyria. Lamoril J; Puy H; Whatley SD; Martin C; Woolf JR; Da Silva V; Deybach JC; Elder GH Am J Hum Genet; 2001 May; 68(5):1130-8. PubMed ID: 11309681 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]