- Secondary hemophagocytic lymphohistiocytosis in SARS-CoV-2 infection2022 | Second Faculty of Medicine
- Hemophagocytic lymphohistiocytosis - diagnostic and therapeutic dilemma2004 | Second Faculty of Medicine
- Hemophagocytic lymphohistiocytosis syndrome2010 | Second Faculty of Medicine, First Faculty of Medicine, Faculty of Physical Education and Sport
- Treatment dilemmas in asymptomatic children with primary hemophagocytic lymphohistiocytosis2018 | Second Faculty of Medicine
- Survival in primary hemophagocytic lymphohistiocytosis 2016-2021: etoposide is better than its reputation2024 | Second Faculty of Medicine
- Lymphohistiocytosis - familial erythrophagocytic2003 | First Faculty of Medicine
- Haemophagocytic lymphohistiocytosis associated with visceral leishmaniasisPublication without faculty affiliation
- Risk factors affecting outcome of unrelated cord blood transplantation for children with familial haemophagocytic lymphohistiocytosis2019 | Second Faculty of Medicine
- Familial haemophagocytic lymphohistiocytosis caused by perforin deficit can be successfully treated by haematopoietic stem cell transplantation - the first diagnosed case in the Czech Republic2006 | Second Faculty of Medicine
- A novel case of homozygous IFNAR1 deficiency with haemophagocytic lymphohistiocytosis2022 | Second Faculty of Medicine
- Hemophagocytic lymphohistiocytosis as a manifestation of visceral leishmaniasis2002 | Second Faculty of Medicine
- Hemophagocytic lymphohistiocytosis associated with visceral leishmaniasis2002 | First Faculty of Medicine
- Detection of chimerism in patient after bone marrow transplation for familial hemophagocytic lymphohistiocytosis2004 | Second Faculty of Medicine, Central Library of Charles University
- Imported visceral leishmaniasis complicated with hemophagocytic lymphohistiocytosisPublication without faculty affiliation
- Perforin deficiency in familial hemophagocytic lymphohistiocytosis (FHL), first diagnosed case in the CR2004 | Second Faculty of Medicine
- Distinct mutations in STXBP2 are associated with variable clinical presentations in patients with familial hemophagocytic lymphohistiocytosis type 5 (FHL5)2012 | Second Faculty of Medicine
- Panniculitis-like T-cell-lymphoma in the mesentery associated with hemophagocytic syndrome: autopsy case report2019 | Second Faculty of Medicine, Third Faculty of Medicine
- Case Report: Systemic Inflammatory Response and Fast Recovery in a Pediatric Patient With COVID-192020 | Second Faculty of Medicine, First Faculty of Medicine
- Hemophagocytic lymfohistiocytosis in adults: Review and case report2018 | Faculty of Medicine in Pilsen
- Clinical similarities and differences of patients with X-linked lymphoproliferative syndrome type 1 (XLP-1/SAP deficiency) versus type 2 (XLP-2/XIAP deficiency)2011 | Second Faculty of Medicine
- X-linked lymphoproliferative disease due to SAP/SH2D1A deficiency: a multicenter study on the manifestations, management and outcome of the disease2011 | Second Faculty of Medicine
- Allogeneic hematopoietic cell transplantation for XIAP deficiency: an international survey reveals poor outcomes2013 | Second Faculty of Medicine
- Infection-associated hemophagocytic syndrome complicated by infectious lymphoproliferation: A case report1996 | Second Faculty of Medicine
- Complications of imported visceral leishmaniasis in childrenPublication without faculty affiliation
- Novel XIAP mutation causing enhanced spontaneous apoptosis and disturbed NOD2 signalling in a patient with atypical adult-onset Crohn's disease2020 | Second Faculty of Medicine
- Allogeneic hematopoietic stem cell transplantation for severe, refractory juvenile idiopathic arthritis2018 | Second Faculty of Medicine
- Transplanxation of Highly Purified Peripheral CD34+ Stem Cells from Haploidenxical Related Donors for Therapy of Children with Nonmalignant Diseases2002 | Second Faculty of Medicine, Central Library of Charles University