Classes
Publications
- Novel SAMD9 Mutation in a Patient With Immunodeficiency, Neutropenia, Impaired Anti-CMV Response, and Severe Gastrointestinal Involvement2019 | First Faculty of Medicine, Second Faculty of Medicine
- Homozygous EXOSC3 Mutation c.92G -> C, p.G31A is a Founder Mutation Causing Severe Pontocerebellar Hypoplasia Type 1 Among the Czech Roma2013 | Second Faculty of Medicine
- Xp21 microdeletion syndrome: Severe cause of adrenal insufficiency, muscular dystrophy, plasma lipid disorder and developmental delay in a two-month-old child with failure to thrive2012 | Second Faculty of Medicine
- NPHP3-Related Disease: A Possible Risk Factor for Developing Encapsulating Peritoneal Sclerosis2024 | Second Faculty of Medicine
- Thirty years of national home parenteral nutrition patient registry2023 | First Faculty of Medicine, Second Faculty of Medicine, Third Faculty of Medicine, Faculty of Medicine in Hradec Králové, Central Library of Charles University
- B cell phenotype and serum levels of interferons, BAFF, and APRIL in multisystem inflammatory syndrome in children associated with COVID-19 (MIS-C)2023 | First Faculty of Medicine, Second Faculty of Medicine, Faculty of Medicine in Pilsen
- Intestinal failure - surgery management and intestinal transplantation2023 | First Faculty of Medicine, Central Library of Charles University
- Severe Acute Kidney Injury in Children as a Rare Complication of Paroxysmal Cold Hemoglobinuria2023 | Second Faculty of Medicine, Central Library of Charles University
- Estimation of glomerular filtration rate from serum creatinine in children2023 | Second Faculty of Medicine, Central Library of Charles University
- Posterior Reversible Encephalopathy Syndrome - A Rare Complication of COVID-19 MIS-C2023 | Second Faculty of Medicine
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