- Trichoblastoma: A Consecutive Series of 349 Sporadic Cases Analyzed by Ackerman Subtypes2021 | Faculty of Medicine in Pilsen
- Carney complex: A clinicopathologic and molecular biological study of a sporadic case, including extracutaneous and cutaneous lesions and a novel mutation of the PRKAR1A gene2009 | Central Library of Charles University
- Carney complex: A clinicopathologic and molecular biological study of a sporadic case, including extracutaneous and cutaneous lesions and a novel mutation of the PRKAR1A gene2009 | First Faculty of Medicine, Faculty of Medicine in Pilsen
- Carney complex: A clinicopathologic and molecular biological study of a sporadic case, including extracutaneous and cutaneous lesions and a novel mutation of the PRKAR1A gene2009 | Central Library of Charles University, Faculty of Medicine in Pilsen
- Clear cell renal cell carcinoma with prominent microvascular hyperplasia: Morphologic, immunohistochemical and molecular-genetic analysis of 7 sporadic cases2022 | Faculty of Medicine in Pilsen
- The importance of advanced parental age in the origin of neurofibromatosis type 12012 | Second Faculty of Medicine
- Genetic screening in adolescents with steroid-resistant nephrotic syndrome2013 | First Faculty of Medicine, Faculty of Physical Education and Sport
- Diagnosis of rotavirus infections in 2004, major characteristics in 1998-2004 in the Czech Republic2006 | Central Library of Charles University
- Diagnosis of rotavirus infections in 2004, major characteristics in 1998-2004 in the Czech Republic2006 | Faculty of Medicine in Pilsen
- TSC2/PKD1 contiguous gene syndrome: A report of 2 cases with emphasis on dermatopathologic findings2009 | Central Library of Charles University
- TSC2/PKD1 contiguous gene syndrome: A report of 2 cases with emphasis on dermatopathologic findings2009 | Faculty of Medicine in Pilsen
- TSC2/PKD1 contiguous gene syndrome: A report of 2 cases with emphasis on dermatopathologic findings2009 | First Faculty of Medicine, Faculty of Medicine in Pilsen
- The significance of rotaviral infection, current possibilities of the vaccination2010 | Faculty of Medicine in Pilsen
- SPAST mutation spectrum and familial occurrence among Czech patients with pure hereditary spastic paraplegia2016 | Second Faculty of Medicine
- Subacute thyroiditis as a cause of thyroid storm. Case report2017 | Central Library of Charles University, Third Faculty of Medicine
- Spondylodiscitis with Abscess Formation in Paravertebral Muscles due to Streptococcus suis - a Case Report2013 | Faculty of Medicine in Hradec Králové
- Tularaemia: Rare Cause of Fever and Lymphadenopathy in an Infant2008 | First Faculty of Medicine, Faculty of Physical Education and Sport, Second Faculty of Medicine
- Mutations in STK11 gene in Czech Peutz-Jeghers patients2009 | Second Faculty of Medicine
- Chapter 4: MITF: A Critical Transcription Factor in Melanoma Transcriptional Regulatory Network2013 | First Faculty of Medicine
- Paroxysmal Kinesigenic Dyskinesia - a Case Report of a Young Woman with Alternating Hemidystonia2009 | Second Faculty of Medicine
- Botulism - a rare but still present, life-threatening disease2019 | Second Faculty of Medicine
- Risk Factors in Ovarian Cancer: A Brief Overview2015 | Central Library of Charles University, First Faculty of Medicine
- Replication of restless legs syndrome loci in three European populations2009 | Central Library of Charles University, First Faculty of Medicine
- Occupational meningitis caused by Streptococcus suis2010 | Publication without faculty affiliation
- Treatment of elderly patients with co-infection with hepatitis B and C viruses2005 | Third Faculty of Medicine
- Mutations in the LMNA gene do not cause axonal CMT in Czech patients2009 | Second Faculty of Medicine
- Confirmation of the GNB4 gene as causal for Charcot-Marie-Tooth disease by a novel de novo mutation in a Czech patient2017 | Second Faculty of Medicine
- Detection of microsatellite instability in Czech HNPCC patients2008 | Second Faculty of Medicine
- Surgical management of colorectal injury in war2023 | Faculty of Medicine in Hradec Králové
- Mutations in the Wilms' tumor 1 gene cause isolated steroid resistant nephrotic syndrome and occur in exons 8 and 92006 | Second Faculty of Medicine