The world's first wiki where authorship really matters (Nature Genetics, 2008). Due credit and reputation for authors. Imagine a global collaborative knowledge base for original thoughts. Search thousands of articles and collaborate with scientists around the globe.

wikigene or wiki gene protein drug chemical gene disease author authorship tracking collaborative publishing evolutionary knowledge reputation system wiki2.0 global collaboration genes proteins drugs chemicals diseases compound
Hoffmann, R. A wiki for the life sciences where authorship matters. Nature Genetics (2008)
MeSH Review

Coproporphyria, Hereditary

Welcome! If you are familiar with the subject of this article, you can contribute to this open access knowledge base by deleting incorrect information, restructuring or completely rewriting any text. Read more.

Disease relevance of Coproporphyria, Hereditary


High impact information on Coproporphyria, Hereditary


Chemical compound and disease context of Coproporphyria, Hereditary


Anatomical context of Coproporphyria, Hereditary


Gene context of Coproporphyria, Hereditary


  1. Uneventful propofol anesthesia in a patient with coexisting hereditary coproporphyria and hereditary angioneurotic edema. Sarantopoulos, C.D., Bratanow, N.C., Stowe, D.F., Kampine, J.P. Anesthesiology (2000) [Pubmed]
  2. 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. Journal of clinical epidemiology. (1996) [Pubmed]
  3. Acquired immunodeficiency syndrome in a patient affected by hereditary coproporphyria: safety of zidovudine treatment. Herrero, C., Bassas, S., Azon, A., Mascaro, J.M., Miro, J. Archives of dermatology. (1990) [Pubmed]
  4. Congenital erythropoietic porphyria: clinical, biochemical, and enzymatic profile of a severely affected infant. Huang, J.L., Zaider, E., Roth, P., Garcia, O., Pollack, S., Poh-Fitzpatrick, M.B. J. Am. Acad. Dermatol. (1996) [Pubmed]
  5. The porphyrias. Moore, M.R., McColl, K.E., Goldberg, A. Diabète & métabolisme. (1979) [Pubmed]
  6. Harderoporphyria: a variant hereditary coproporphyria. Nordmann, Y., Grandchamp, B., de Verneuil, H., Phung, L., Cartigny, B., Fontaine, G. J. Clin. Invest. (1983) [Pubmed]
  7. Coproporphyrinogen-oxidase deficiency in hereditary coproporphyria. Nordmann, Y., Grandchamp, B., Phung, N., de Verneuil, H., Grelier, M., Neiré, J. Lancet (1977) [Pubmed]
  8. Characterization of the heme synthesis enzyme coproporphyrinogen oxidase (CPO) in zebrafish erythrogenesis. Hanaoka, R., Katayama, S., Dawid, I.B., Kawahara, A. Genes Cells (2006) [Pubmed]
  9. Occurrence of hepatocellular carcinoma in a case of hereditary coproporphyria. Andant, C., Puy, H., Deybach, J.C., Soulé, J.C., Nordmann, Y. Am. J. Gastroenterol. (1997) [Pubmed]
  10. Identification of a novel mutation of the CPO gene in a Japanese hereditary coproporphyria family. Susa, S., Daimon, M., Kondo, H., Kondo, M., Yamatani, K., Sasaki, H. Am. J. Med. Genet. (1998) [Pubmed]
  11. Acute hereditary coproporphyria induced by the androgenic/anabolic steroid methandrostenolone (Dianabol). Lane, P.R., Massey, K.L., Worobetz, L.J., Jutras, M.N., Hull, P.R. J. Am. Acad. Dermatol. (1994) [Pubmed]
  12. Induction of anaesthesia with ketamine during an acute crisis of hereditary coproporphyria. Capouet, V., Dernovoi, B., Azagra, J.S. Canadian journal of anaesthesia = Journal canadien d'anesthésie. (1987) [Pubmed]
  13. Effects of erythromycin on gut transit in pseudo-obstruction due to hereditary coproporphyria. Vassallo, M.J., Camilleri, M., Sullivan, S.N., Thomforde, G.M. J. Clin. Gastroenterol. (1992) [Pubmed]
  14. Normeperidine-induced seizures in hereditary coproporphyria. Deeg, M.A., Rajamani, K. South. Med. J. (1990) [Pubmed]
  15. Prevention of premenstrual exacerbation of hereditary coproporphyria by gonadotropin-releasing hormone analogue. Yamamori, I., Asai, M., Tanaka, F., Muramoto, A., Hasegawa, H. Intern. Med. (1999) [Pubmed]
  16. Hereditary coproporphyria: unusual nervous system involvement in two cases. Casali, C., Lo Monaco, M., D'Alessandro, L., Griso, D., Amantea, A., Topi, G.C., Tonali, P. J. Neurol. (1984) [Pubmed]
  17. Molecular characterization of porphyrias in Italy: a diagnostic flow-chart. Martinez di Montemuros, F., Di Pierro, E., Patti, E., Tavazzi, D., Danielli, M.G., Biolcati, G., Rocchi, E., Cappellini, M.D. Cell. Mol. Biol. (Noisy-le-grand) (2002) [Pubmed]
  18. Oxygen-dependent coproporphyrinogen-III oxidase from Escherichia coli: one-step purification and biochemical characterisation. Macieira, S., Martins, B.M., Huber, R. FEMS Microbiol. Lett. (2003) [Pubmed]
  19. Mutations in human CPO gene predict clinical expression of either hepatic hereditary coproporphyria or erythropoietic harderoporphyria. Schmitt, C., Gouya, L., Malonova, E., Lamoril, J., Camadro, J.M., Flamme, M., Rose, C., Lyoumi, S., Da Silva, V., Boileau, C., Grandchamp, B., Beaumont, C., Deybach, J.C., Puy, H. Hum. Mol. Genet. (2005) [Pubmed]
  20. Coexistence of hereditary coproporphyria and epilepsy: coproporphyrinogen oxidase deficiency in liver and kidney. Doss, M., von Tiepermann, R., Pflüger, K.H. J. Neurol. (1981) [Pubmed]
WikiGenes - Universities