- SHOX gene deficiency - a cause of familial short stature2010 | Second Faculty of Medicine
- Defect in the SHOX gene as a cause of short stature - a case report2012 | Second Faculty of Medicine
- Growth disorders due to rearrangement of SHOX gene locus2019 | Faculty of Medicine in Pilsen
- SHOX gene deficiency - a cause of familial short stature.2010 | First Faculty of Medicine
- SHOX gene polymorphic variants and their association with isolated short staturePublication without faculty affiliation
- Complex genetic analysis of SHOX gene in patients with dyschondrosteosis or idiopathic short staturePublication without faculty affiliation
- Léri-Weill Syndrome on the Principle of Structural Aberration of Chromosome Y (Case Report)2018 | Faculty of Medicine in Pilsen
- Analysis of common SHOX gene sequence variants and similar to 4.9-kb PAR1 deletion in ISS patients +12014 | Faculty of Science, First Faculty of Medicine
- SHOX gene defects and selected dysmorphic signs in patients of idiopathic short stature and Léri-Weill dyschondrosteosis2012 | Faculty of Science, First Faculty of Medicine
- Prepubertal Girls With Turner Syndrome and Children With Isolated SHOX Deficiency Have Similar Bone Geometry at the Radius2013 | Faculty of Science, First Faculty of Medicine, Faculty of Mathematics and Physics, Second Faculty of Medicine
- Acute lymphoblastic leukemia in a child with Leri-Weill syndrome and complete SHOX gene deletion: A Case Report2018 | Second Faculty of Medicine
- SHOX gene defects and selected dysmorphic signs in patients of idiopathic short stature and Leri-Weill dyschondrosteosis2012 | First Faculty of Medicine
- Growth hormone therapy in pediatrics. Past and Present2011 | Second Faculty of Medicine
- PAR1 deletion/duplication in patients with dyschondrosteosis or idiopathic short staturePublication without faculty affiliation
- Bone Geometry and Volumetric Bone Density at the Radius in Patients with Isolated SHOX Deficiency2013 | Faculty of Science, First Faculty of Medicine, Faculty of Mathematics and Physics, Second Faculty of Medicine
- Použití metody MLPA při diagnostice delecí SHOX genuPublication without faculty affiliation
- Detection of SHOX gene aberrations in routine diagnostic practice and evaluation of phenotype scoring form effectiveness2017 | First Faculty of Medicine
- The MLPA Metod in diagnostic of SHOX gene and PAR1 deletionsPublication without faculty affiliation
- Twenty years of "authentic" recombinant growth hormone in the treatment of pediatric patients2007 | Second Faculty of Medicine
- Comparison of SHOX and associated elements duplications distribution between patients (Lėri-Weill dyschondrosteosis/idiopathic short stature) and population sample2017 | Faculty of Science, First Faculty of Medicine
- Growth plate disorders causing familiar short stature2018 | Second Faculty of Medicine
- Current status of teatment of growth disorders2012 | Faculty of Medicine in Pilsen
- Contemporary therapy of growth disorders2015 | Faculty of Medicine in Pilsen
- Gregor Mendel and regulation of child's growth: genes, molecules, and paediatric clinical routine2022 | Second Faculty of Medicine
- Delece 18p v mozaice u pacienta s fenotypem připomínajícím syndrom Noonanové2016 | First Faculty of Medicine, Faculty of Mathematics and Physics, Second Faculty of Medicine, Faculty of Physical Education and Sport
- Rare congenital chromosomal aberration dic(X;Y)(p22.33;p11.32) in a patient with primary myelofibrosis2016 | First Faculty of Medicine, Central Library of Charles University
- A Rare Variant of Turner Syndrome in Four Sequential Generations: Effect of the Interplay of Growth Hormone Treatment and Estrogens on Body Proportion2016 | Second Faculty of Medicine
- Genetic testing of children with familial tall stature: is it worth doing?2024 | Second Faculty of Medicine
- Muscle function in Turner syndrome: normal force but decreased power2015 | Faculty of Mathematics and Physics, Second Faculty of Medicine