Publications
- A New Mutation within the Porphobilinogen Deaminase Gene Leading to a Truncated Protein as a Cause of Acute Intermittent Porphyria in an Extended Indian Family2007 | First Faculty of Medicine
- Acute intermittent porphyria: New mutations found in the porphobilinogen deaminase gene in Czech and Slovak patientsPublication without faculty affiliation
- Molecular patology of hereditary coproporphyriaPublication 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
- Molecular pathology of heme biosynthesis. Porphobilinogen deaminase: Novel mutation in Czech and Slovak patients with acute intermittent porphuriaPublication without faculty affiliation
- Two special Case of acute intermittent porphyria: molecular biological studyPublication without faculty affiliation
- Akutní intermitentní porfyrie: Molekulárně biochemická studiePublication without faculty affiliation
- Acute intermittent porphyria: impact of newly found mutations on the biochemical and enzymatical protein properties (2)Publication without faculty affiliation
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