Publications
- Mutations in human CPO gene predict clinical expression of either hepatic hereditary coproporphyria or erythropoietic harderoporphyria2005 | First Faculty of Medicine
- Menke´s disease and respiratory chain abnormalities2001 | First Faculty of Medicine
- Congenital erythropoetic porphyriaPublication without faculty affiliation
- Homozygous form of porphyria variegata in childhoodPublication without faculty affiliation
- Congenital Erythropoietic Porphyria (Gunther Disease)Publication without faculty affiliation
- Human coproporphyrinogen oxidase: biochemical characterization of wild-type enzyme and its naturally occurring R331W mutant formPublication without faculty affiliation
- In frame deletion of glycin 390 in coproporphyrinogen oxidase gene as a cause of hereditary coproporphyriaPublication without faculty affiliation
- Hereditary coproporphyria due to delection of one amino acid of one czech familyPublication without faculty affiliation
- Eyrthropoetic protoporphyriaPublication without faculty affiliation
- Variegate porfihyria childhood: compound heterozygosity in protoporhyrinogen oxidase genePublication without faculty affiliation
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