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
- De Novo Mutation Found in the Porphobilinogen Deaminase Gene in Slovak Acute Intermittent Porphyria Patient: Molecular Biochemical Study2006 | First Faculty of Medicine
- Novel mutation in Porphobilinogen deaminase gene in a family with acute intermittent porphyria from NepalPublication without faculty affiliation
- Molecular analysis of the porphobilinogen deaminase gene in newly (2004) diagnozed Czech and Slovak acute intermittent porphyria patients: Report of three novel mutationsPublication without faculty affiliation
- Novel mutations in the porphobilinogen deaminase gene in Czech and Slovak acute intermittent porphyria patientsPublication without faculty affiliation
- Acute intermittent porphyria: identification of three novel mutations in the porphobilinogen deaminase gene in Czech and Slovak patientsPublication without faculty affiliation
- Novel mutations in the porphobilinogen deaminase gene in Czech acute intermittent porphyria patiensPublication without faculty affiliation
- Two special Case of acute intermittent porphyria: molecular biological studyPublication without faculty affiliation
- Low Birth Weight is Associated witj More Severe Course of Steroid-Sensitive Nephrotic Syndrome in Children, Multicentric Study2024 | First Faculty of Medicine, Second Faculty of Medicine, Faculty of Science, Faculty of Medicine in Hradec Králové, Faculty of Medicine in Pilsen
- Low Birth Weight is Associated with More Severe Course of Steroid-Sensitive Nephrotic Syndrome in Children, Multicentric Study2024 | Second Faculty of Medicine, Faculty of Science
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