|1.||Higuchi, Keiichi: 1 article (07/2013)|
|2.||Hiai, Hiroshi: 1 article (07/2013)|
|3.||Taketani, Shigeru: 1 article (07/2013)|
|4.||Mori, Masayuki: 1 article (07/2013)|
|5.||Gotoh, Saki: 1 article (07/2013)|
|6.||Aurizi, C: 1 article (01/2009)|
|7.||Sorge, F: 1 article (01/2009)|
|8.||Usai, G: 1 article (01/2009)|
|9.||Barbieri, L: 1 article (01/2009)|
|10.||Macrì, A: 1 article (01/2009)|
|1.||Hereditary Coproporphyria (Coproporphyrinogen Oxidase Deficiency)
01/01/2009 - "Here we report the characterization of four novel mutations and a previously described one of the coproporphyrinogen III oxidase (CPO) gene in five Italian patients affected by Hereditary Coproporphyria (HCP). "
01/01/2003 - "Coproporphyrinogen III oxidase is deficient in hereditary coproporphyria. "
09/01/1983 - "Both parents showed only mild abnormalities in porphyrin excretion and lymphocyte coproporphyrinogen III oxidase activity decreased to 50% of normal values, as is expected in heterozygous cases of hereditary coproporphyria. "
04/30/1977 - "This finding suggests that decreased coproporphyrinogen III oxidase activity reflects the primary genetic defect in Hereditary Coproporphyria. "
04/30/1977 - "We measured lymphocytes Coproporphyrinogen III Oxidase activity in 17 subjects with hereditary coproporphyria. "
|2.||Hepatic Porphyrias (Hepatic Porphyria)
10/15/2005 - "Hereditary coproporphyria (HCP), an autosomal dominant acute hepatic porphyria, results from mutations in the gene that encodes coproporphyrinogen III oxidase (CPO). "
01/01/1999 - "Hereditary coproporphyria (HC) is an acute hepatic porphyria with autosomal dominant inheritance caused by deficient activity of coproporphyrinogen III oxidase (CPO). "
02/15/1998 - "Hereditary coproporphyria (HC) is an acute hepatic porphyria with autosomal dominant inheritance caused by deficient activity of coproporphyrinogen III oxidase (COX). "
02/01/1980 - "The excretion of position isomers of type III porphyrins, not only in porphyric disorders in which the enzymatic decarboxylation of uroporphyrinogen III to coproporphyrinogen III is known to or suspected to play a role, but also in normal man and in conditions like erythropoietic protoporphyria and lead-intoxication, in which no such changes have ever been reported, or would be expected for theoretical reasons, has been described. "
|4.||Inborn Genetic Diseases (Disease, Hereditary)
|5.||Porphyria Cutanea Tarda
|3.||protoporphyrinogen (protoporphyrinogen IX)
|5.||Uroporphyrinogen Decarboxylase (Uroporphyrinogen III Decarboxylase)
|10.||Coproporphyrinogen Oxidase (Coproporphyrinogen III Oxidases)