Publications
- Acute intermittent porphyria: New mutations found in the porphobilinogen deaminase gene in Czech and Slovak patientsPublication without faculty affiliation
- Varied psychiatric and neurologic manifestations of acute hepatic porphyrias, metabolic genetic disorders of heme bisynthesisPublication without faculty affiliation
- Novel mutations in the porphobilinogen deaminase gene in Czech acute intermittent porphyria patiensPublication without faculty affiliation
- Molecular pathology of two special cases of acute intermittent porphyriaPublication without faculty affiliation
- Two special Case of acute intermittent porphyria: molecular biological studyPublication without faculty affiliation
- Red and Yellow, Defects on the Heme Pathway. Hereditary Coproporphyria and Gilbert's Syndrome in a Czech FamilyPublication without faculty affiliation
- Porphyria Variegata - Diagnostics and Treatment DifficultiesPublication without faculty affiliation
- Purple and Yellow. Hereditary Coproporphyria and Gilbert's Syndrome in Czech FamilyPublication without faculty affiliation
- Nové mutace v genu pro koproporfyrinogenoxidázuPublication without faculty affiliation
- Molekulární patologie hereditární koproporfyriePublication without faculty affiliation
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