Publications
- Genetic Polymorphisms of UGT 1A1*28 in the TATA-box Promoter Region of Bilirubin Uridinediphosphate-glucuronosyltransferase Gene in Children with Gilbert's Syndrome2005 | Second Faculty of Medicine
- Molecular genetic analysis of steroid 21-hydroxylase gene2004 | Second Faculty of Medicine
- Common CYP21 gene mutations in Czech patients and statistical analysis of worldwide mutation distribution2003 | Second Faculty of Medicine, Central Library of Charles University
- Hypothalamic neuropeptides involved in food intake and regulation of energy homeostasis2003 | Second Faculty of Medicine
- Frequency of CYP21 gene mutations in Czech patients with steroid 21-hydroxylase deficiency and statistical comparison with other populations2003 | Second Faculty of Medicine
- Plasma DNA - a New Laboratory marker for Non-invasive Measurement of Cell Death2002 | Second Faculty of Medicine
- Amylin--its physiological role in humans2002 | Second Faculty of Medicine
- Mutation detection in the CYP21B gene determining virilized and non-classical forms of steroid 21-hydroxylase deficiency2000 | Second Faculty of Medicine, Central Library of Charles University
- Use of Fourier transform infrared (FTIR) spectroscopy to detect rarely occurring cyanoacrylate and pyrophosphate urine stones2023 | First Faculty of Medicine, Faculty of Physical Education and Sport, Second Faculty of Medicine, Central Library of Charles University
- Study of Metallothionein Levels in the Serum of Patients with Malignant Tumour2023 | First Faculty of Medicine, Second Faculty of Medicine, Central Library of Charles University
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