Publications
- Human coproporphyrinogen oxidase (CPO): Biochemical characterization of wild-type enzyme and its naturally occurring mutant formsPublication without faculty affiliation
- Biochemical Characterization of Wild-type Human CoproporphyrinogenOxidase (CPO) and Its Naturally Occurring Mutant FormsPublication without faculty affiliation
- Structure-function relationship studies of human coproporphyrinogen oxidase (CPO), biochemical characterization of wild-type and mutant formsPublication 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
- Abnormal kidney ultrasound and function in a five-year-old boy born prematurely with a birth weight of 370 grams2023 | Second Faculty of Medicine, Third Faculty of Medicine
- Severe Acute Kidney Injury in Children as a Rare Complication of Paroxysmal Cold Hemoglobinuria2023 | Second Faculty of Medicine, Central Library of Charles University
- Shared decision-making and goals of care setting in a child with progressive renal failure caused by primary hyperoxaluria2023 | First Faculty of Medicine
- Molecular Diagnostics of Copper-Transporting Protein Mutations Allows Early Onset Individual Therapy of Menkes Disease2017 | First Faculty of Medicine
- 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
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