Homozygous case of hereditary coproporphyria - PubMed (original) (raw)
Case Reports
Homozygous case of hereditary coproporphyria
B Grandchamp et al. Lancet. 1977 Dec.
No abstract available
Similar articles
- [Hereditary coproporphyria].
Gregor A, Kostrzewska E, Zywiecka M. Gregor A, et al. Pol Arch Med Wewn. 1981 Jul;66(1):25-31. Pol Arch Med Wewn. 1981. PMID: 7291025 Polish. No abstract available. - [Hereditary coproporphyria. A familial study].
Rocchi E, Pietrangelo A, Gibertini P, Cassanelli M, Trenti T, Borghi A, Silingardi M, Jensen J, Ventura E. Rocchi E, et al. Recenti Prog Med. 1984 Feb;75(2):123-31. Recenti Prog Med. 1984. PMID: 6729195 Italian. No abstract available. - [Hereditary coproporphyria in the Federal Republic of Germany (author's transl)].
Doss M, von Tiepermann R, Verspohl F. Doss M, et al. J Clin Chem Clin Biochem. 1978 Sep;16(9):519-24. J Clin Chem Clin Biochem. 1978. PMID: 712343 German. No abstract available. - [Alcohol-induced changes of porphyrin metabolism (author's transl)].
Doss M. Doss M. Leber Magen Darm. 1978 Oct;8(5):278-85. Leber Magen Darm. 1978. PMID: 359965 Review. German. - Alcohol and porphyrin metabolism.
Doss MO, Kühnel A, Gross U. Doss MO, et al. Alcohol Alcohol. 2000 Mar-Apr;35(2):109-25. doi: 10.1093/alcalc/35.2.109. Alcohol Alcohol. 2000. PMID: 10787385 Review.
Cited by
- BALB.NCT-Cpox nct is a unique mouse model of hereditary coproporphyria.
Kang X, Shimada S, Miyahara H, Higuchi K, Mori M. Kang X, et al. Mol Genet Metab Rep. 2023 Mar 16;35:100964. doi: 10.1016/j.ymgmr.2023.100964. eCollection 2023 Jun. Mol Genet Metab Rep. 2023. PMID: 36967721 Free PMC article. - Murine models of the human porphyrias: Contributions toward understanding disease pathogenesis and the development of new therapies.
Yasuda M, Desnick RJ. Yasuda M, et al. Mol Genet Metab. 2019 Nov;128(3):332-341. doi: 10.1016/j.ymgme.2019.01.007. Epub 2019 Jan 18. Mol Genet Metab. 2019. PMID: 30737139 Free PMC article. Review. - Recent advances on porphyria genetics: Inheritance, penetrance & molecular heterogeneity, including new modifying/causative genes.
Yasuda M, Chen B, Desnick RJ. Yasuda M, et al. Mol Genet Metab. 2019 Nov;128(3):320-331. doi: 10.1016/j.ymgme.2018.11.012. Epub 2018 Nov 30. Mol Genet Metab. 2019. PMID: 30594473 Free PMC article. Review. - Neonatal-Onset Hereditary Coproporphyria: A New Variant of Hereditary Coproporphyria.
Hasegawa K, Tanaka H, Yamashita M, Higuchi Y, Miyai T, Yoshimoto J, Okada A, Suzuki N, Iwatsuki K, Tsukahara H. Hasegawa K, et al. JIMD Rep. 2017;37:99-106. doi: 10.1007/8904_2017_20. Epub 2017 Mar 28. JIMD Rep. 2017. PMID: 28349448 Free PMC article. - Harderoporphyria due to homozygosity for coproporphyrinogen oxidase missense mutation H327R.
Hasanoglu A, Balwani M, Kasapkara CS, Ezgü FS, Okur I, Tümer L, Cakmak A, Nazarenko I, Yu C, Clavero S, Bishop DF, Desnick RJ. Hasanoglu A, et al. J Inherit Metab Dis. 2011 Feb;34(1):225-31. doi: 10.1007/s10545-010-9237-9. Epub 2010 Nov 20. J Inherit Metab Dis. 2011. PMID: 21103937 Free PMC article.