- Endocrine and paediatric features of Noonan syndrom2015 | Faculty of Medicine in Hradec Králové
- And your diagnosis? 1st part. (Protracted febrility with dyspnoea at Noonan's syndrome girl)2005 | Publication without faculty affiliation
- And your diagnosis? 2nd part. (Protracted febrility with dyspnoea at Noonan's syndrome girl)2005 | Publication without faculty affiliation
- Noonan's syndrome - common among "rare diseases"2020 | Second Faculty of Medicine
- The clinical significance of A2ML1 variants in Noonan syndrome has to be reconsidered2021 | Second Faculty of Medicine
- Noonan syndrome and other RASopathies: Aetiology, diagnostic procedures and therapy2020 | Second Faculty of Medicine
- Noonan syndrome with multiple lentigines and congenital myotonic dystrophy type I in a newborn2019 | Faculty of Medicine in Pilsen
- Activating Mutations Affecting the Dbl Homology Domain of SOS2 Cause Noonan Syndrome2015 | Second Faculty of Medicine
- Genotype and phenotype in patients with Noonan syndrome and a RIT1 mutation2016 | Second Faculty of Medicine
- A novel heterozygous RIT1 mutation in a patient with Noonan syndrome, leukopenia, and transient myeloproliferation-a review of the literature2016 | Second Faculty of Medicine, First Faculty of Medicine, Faculty of Physical Education and Sport
- European Medical Education Initiative on Noonan syndrome: A clinical practice survey assessing the diagnosis and clinical management of individuals with Noonan syndrome across Europe2022 | Second Faculty of Medicine
- Prenatal phenotype of RASopathies2020 | Publication without faculty affiliation
- Noonan syndrom with multiple lentigines and congenital myotonic dystrophy type 1 in a newborn2020 | Faculty of Medicine in Pilsen
- Management of cardiac aspects in children with Noonan syndrome - results from a European clinical practice survey among paediatric cardiologists2022 | Second Faculty of Medicine
- A restricted spectrum of NRAS mutations causes Noonan syndrome2010 | Second Faculty of Medicine
- Management of growth failure and other endocrine aspects in patients with Noonan syndrome across Europe: A sub-analysis of a European clinical practice survey2022 | Second Faculty of Medicine
- The mutational spectrum of PTPN11 in juvenile myelomonocytic leukemia and Noonan syndrome/myeloproliferative disease2005 | Second Faculty of Medicine
- Novel BRAF mutation in a patient with LEOPARD syndrome and normal intelligence2009 | Second Faculty of Medicine
- Germline CBL mutations cause developmental abnormalities and predispose to juvenile myelomonocytic leukemia2010 | Second Faculty of Medicine
- Refinement of evolutionary medicine predictions based on clinical evidence for the manifestations of Mendelian diseases2019 | Third Faculty of Medicine
- Modeling age-specific facial development in Williams-Beuren-, Noonan-, and 22q11.2 deletion syndromes in cohorts of Czech patients aged 3-18 years: A cross-sectional three-dimensional geometric morphometry analysis of their facial gestalt2018 | Second Faculty of Medicine, Faculty of Science, Faculty of Mathematics and Physics
- Coarctation of the Aorta in Noonan-Like Syndrome With Loose Anagen Hair2014 | Second Faculty of Medicine
- Mutagenic effect of advanced paternal age in neurocardiofaciocutaneous syndrome2014 | Second Faculty of Medicine
- Eva Seemanova 80 Years - International Medical Genetics, Prague 1971-20162019 | Second Faculty of Medicine