- Secondary hemophagocytic lymphohistiocytosis in SARS-CoV-2 infection2022 | Second Faculty of Medicine
- Lipoprotein Lipase Deficiency: Clinical, Biochemical and Molecular Characteristics in Three Patients with Novel Mutations in the LPL Gene2014 | First Faculty of Medicine
- Chronic visceral acid sphingomyelinase deficiency (Niemann-Pick disease type B) in 16 Polish patients: long-term follow-up2019 | First Faculty of Medicine
- Evaluation of different suspicion indices in identifying patients with Niemann-Pick disease Type C in clinical practice: a post hoc analysis of a retrospective chart review2019 | First Faculty of Medicine
- Adult onset Still's disease with focus on differential diagnostics and treatment2017 | First Faculty of Medicine
- Evans' syndrome in a child with diabetes mellitus1998 | Second Faculty of Medicine
- Febrile pancytopenia and hepato-splenomegaly as leading symptoms of visceral leishmaniasis2012 | First Faculty of Medicine
- Visceral leishmaniasis - editorial2012 | Faculty of Medicine in Pilsen
- Considered gastrointestinal reflux disease symptoms2016 | Second Faculty of Medicine
- Hemophagocytic lymphohistiocytosis as a manifestation of visceral leishmaniasis2002 | Second Faculty of Medicine
- Systematic mastocytosis2010 | Third Faculty of Medicine
- Transient myeloproliferative syndrome in newborn without Down syndrome phenotype: a unique case report2019 | First Faculty of Medicine
- The role of interleukin 6 in the pathogenesis and therapy of Castleman disease - an immunologist's perspective2023 | Second Faculty of Medicine
- Congenital Toxoplasmosis: Possibilities for Laboratory Diagnosis2005 | First Faculty of Medicine
- Infectious mononucleosis2005 | Second Faculty of Medicine
- Diagnosis and Treatment Options for Niemann-Pick Disease Type C2012 | First Faculty of Medicine, Third Faculty of Medicine
- Infection-associated hemophagocytic syndrome complicated by infectious lymphoproliferation: A case report1996 | Second Faculty of Medicine
- Mastocytoses2018 | First Faculty of Medicine
- Pediatric Precursor B-Cell Lymphoblastic Malignancies: From Extramedullary to Medullary Involvement2022 | Second Faculty of Medicine
- Hemophagocytic lymphohistiocytosis - diagnostic and therapeutic dilemma2004 | Second Faculty of Medicine
- A novel mutation in the coding region of the prosaposin gene leads to a complete deficiency of prosaposin and saposins, and is associated with a complex sphingolipidosis dominated by lactosylceramide accumulation2001 | First Faculty of Medicine
- Acid Ceramidase Deficiency in Mice Leads to Severe Ocular Pathology and Visual Impairment2019 | First Faculty of Medicine
- A novel heterozygous RIT1 mutation in a patient with Noonan syndrome, leukopenia, and transient myeloproliferation-a review of the literature2016 | First Faculty of Medicine, Second Faculty of Medicine, Faculty of Physical Education and Sport
- Congenital and postnatal cytomegalovirus infections2022 | Second Faculty of Medicine
- Mucopolysaccharidosis I - clinical manifestations in 24 children from the Czech Republic and Slovakia2011 | Second Faculty of Medicine
- Neural cells generated from human induced pluripotent stem cells as a model of CNS involvement in mucopolysaccharidosis type II2018 | First Faculty of Medicine
- Hepatic pathology and altered gene transcription in a murine model of acid ceramidase deficiency2019 | First Faculty of Medicine
- Hemophagocytic lymphohistiocytosis syndrome2010 | First Faculty of Medicine, Second Faculty of Medicine, Faculty of Physical Education and Sport
- Male patient with ALG13 associated congenital disorder of glycosylation2021 | Second Faculty of Medicine
- Paediatric diabetes subtypes in a consanguineous population: a single-centre cohort study from Kurdistan, Iraq2024 | Second Faculty of Medicine