- Nijmegen Breakage Syndrome - neglected primary immunodeficiency2012 | Second Faculty of Medicine
- Nijmegen breakage syndrome in Slovakia2004 | Second Faculty of Medicine
- Nijmegen Breakage Syndrome (NBS)1999 | Second Faculty of Medicine
- Increased Risk of Malignancies in Heterozygotes in Families of Patients with Nijmegen Breakage Syndrome2006 | Second Faculty of Medicine
- Nijmegen breakage syndrome in 13% of age-matched Czech children with primary microcephaly2004 | Second Faculty of Medicine
- The gene for the ataxia-telangiectasia variant, Nijmegen breakage syndrome, maps to a 1-cM interval on chromosome 8q211997 | Second Faculty of Medicine
- Telomere attrition and dysfunction: a potential trigger of the progeroid phenotype in nijmegen breakage syndrome2020 | Second Faculty of Medicine
- Nijmegen breakage syndrome2000 | Second Faculty of Medicine
- Nijmegen breakage syndrome (NBS) with neurological abnormalities and without chromosomal instability2006 | Second Faculty of Medicine
- Radiation-induced DNA damage and repair in peripheral blood mononuclear cells from Nijmegen breakage syndrome patients and carriers assessed by the Comet assay2006 | Second Faculty of Medicine
- Clinical variability and expression of the NBN c.657del5 allele in Nijmegen Breakage Syndrome2009 | Second Faculty of Medicine
- Cancer incidence in Nijmegen breakage syndrome is modulated by the amount of a variant NBS protein2007 | Second Faculty of Medicine
- Extreme variation in apoptosis capacity amongst lymphoid cells of Nijmegen breakage syndrome patients2008 | Second Faculty of Medicine
- Nibrin, a novel DNA double-strand break repair protein, is mutated in nijmegen breakage syndrome1998 | Second Faculty of Medicine
- Clinical ascertainment of Nijmegen breakage syndrome (NBS) and prevalence of the major mutation, 657de15, in three Slav populations2000 | Second Faculty of Medicine
- Rescue of a telomere length defect of Nijmegen breakage syndrome cells requires NBS and telomerase catalytic subunit2001 | Second Faculty of Medicine
- Germline mutations 657del5 and 643C > T (R215W) in NBN are not likely to be associated with increased risk of breast cancer in Czech women2012 | First Faculty of Medicine
- Syndromes of chromosomal instability2014 | Second Faculty of Medicine
- Cancer risk of heterozygotes with the NBN founder mutation2007 | Second Faculty of Medicine
- The Slavic NBN Founder Mutation: A Role for Reproductive Fitness?2016 | First Faculty of Medicine, Second Faculty of Medicine, Faculty of Physical Education and Sport
- Non-Hodgkin lymphoma and pre-existing conditions: spectrum, clinical characteristics and outcome in 213 children and adolescents2016 | Second Faculty of Medicine
- Heterozygous carriers of Slavic mutation 657del5 of NBN gene in patients with colorectal cancer2011 | Second Faculty of Medicine
- Mutations in tumor suppressor gene NBS1 in adult patients with malignancies2006 | Second Faculty of Medicine
- Tumor supressor gene NBS1 among children patients with malignancies2004 | First Faculty of Medicine, Second Faculty of Medicine, Faculty of Physical Education and Sport
- NBN 657del5 heterozygous mutations and colorectal cancer risk in the Czech Republic2009 | First Faculty of Medicine, Second Faculty of Medicine, Third Faculty of Medicine
- Radiotherapy and radiosensitivity syndromes in DNA repair gene mutations2022 | First Faculty of Medicine
- The NBN founder mutation-Evidence for a country specific difference in age at cancer manifestation2023 | Second Faculty of Medicine
- Eva Seemanova 80 Years - International Medical Genetics, Prague 1971-20162019 | Second Faculty of Medicine