- Mulibrey Nanism and Wilms Tumor1999 | Second Faculty of Medicine
- Molecular Genetics of the Wilms' Tumor2001 | Second Faculty of Medicine
- Adult Wilm's tumor - a rare case2017 | Publication without faculty affiliation
- Allele loss in Wilms tumors of chromosome arms 11q, 16q, and 22q correlates with clinicopathological parameters1998 | Second Faculty of Medicine
- Wilms' tumor gene 1 (WT1) aberrations in testicular germ cell tumors (TGCTs)Publication without faculty affiliation
- Wilms tumor gene 1 (WT1), TP53, RAS/BRAF and KIT aberrations in testicular germ cell tumors2016 | First Faculty of Medicine, Second Faculty of Medicine, Central Library of Charles University, Third Faculty of Medicine
- Mutations in the Wilms' tumor 1 gene cause isolated steroid resistant nephrotic syndrome and occur in exons 8 and 92006 | Second Faculty of Medicine
- Real-time PCR quantification of major Wilms' tumor gene 1 (WT1) isoforms in acute myeloid leukemia, their characteristic expression patterns and possible functional consequences +12012 | Second Faculty of Medicine
- Aniridia, Gonadoblastoma, Wilms tumor and deletion 11p131998 | Publication without faculty affiliation
- Wilms' tumor gene 1 (WT1) expression in childhood acute lymphoblastic leukemia: a wide range of WT1 expression levels, its impact on prognosis and minimal residual disease monitoring2006 | Second Faculty of Medicine
- Regulatory element methylation of WT1 gene in patients with Wilms tumor2000 | Second Faculty of Medicine
- Clinical relevance of Wilms tumor 1 gene mutations in childhood acute myeloid leukemia2009 | Second Faculty of Medicine
- Nephroblastoma - current evaluation and treatment2016 | Second Faculty of Medicine
- Methylation pathern i WT1 promoter and enhancer regions by patients with Wilms tumor2000 | Second Faculty of Medicine
- Nephroblastoma - 30-years period of its treatment in the University Hospital Motol, Prague2013 | First Faculty of Medicine, Faculty of Physical Education and Sport, Second Faculty of Medicine
- Mutations in the Wilms´tumor 1 gene cause isolated steroid resistant nephrotic syndrome and occur in exons 8 and 9 +12006 | Publication without faculty affiliation
- MRI Characteristics of Pediatric Renal Tumors: A SIOP-RTSG Radiology Panel Delphi Study2022 | Second Faculty of Medicine
- Surgical tactics in the treatment of malignant renal tumors in childhood1997 | Second Faculty of Medicine
- Fanconi anemia with biallelic FANCD1/BRCA2 mutations - Case report of a family with three affected children2016 | Second Faculty of Medicine
- Alteration in DNA-binding affinity of Wilms tumor 1 protein due to WT1 genetic variants associated with steroid - resistant nephrotic syndrome in children2022 | Second Faculty of Medicine
- Fanconi Anemia, Complementation Group D1 Caused by Biallelic Mutations of BRCA2 Gene - Case Report2016 | Second Faculty of Medicine
- Methylation changes in promoter and enhancer regions of the WT1 gene in Wilms'tumours2001 | Second Faculty of Medicine
- Distinct clinicopathological features in metanephric adenoma harboring BRAF mutation2017 | Faculty of Medicine in Pilsen
- Expression of four major WT1 splicing variants in acute and chronic myeloid leukemia patients analyzed by newly developed four real-time RT PCRs2012 | Faculty of Science
- Surgical Treatment of Renal Fusion Anomalies2007 | Second Faculty of Medicine
- Gene encoding a new RING-B-box-Coiled-coil protein is mutated in mulibrey nanism2000 | Second Faculty of Medicine
- Genotype/Phenotype Correlation in Nephrotic Syndrome Caused by WT1 Mutations2010 | Second Faculty of Medicine
- Heterogeneous MYCN amplification in neuroblastoma: a SIOP Europe Neuroblastoma Study2018 | Second Faculty of Medicine