Publikace
- The genetic landscape of children born small for gestational age with persistent short stature (SGA-SS)2024 | 2. lékařská fakulta
- Analysis of children with familial short stature: who should be indicated for genetic testing?2023 | 2. lékařská fakulta
- Search for a time- and cost-saving genetic testing strategy for maturity-onset diabetes of the young2022 | 2. lékařská fakulta, Matematicko-fyzikální fakulta
- A case of digenic maturity onset diabetes of the young with heterozygous variants in both HNF1Α and HNF1Β genes2021 | 2. lékařská fakulta
- Monogenně podmíněný diabetes MODY v dětském věku: retrospektivní studie pacientů dignostikovaných na Dětské klinice FN Plzeň v letech 2000-20172019 | 2. lékařská fakulta, Lékařská fakulta v Plzni
- Screening of monogenic autoimmune diabetes among children with type 1 diabetes and multiple autoimmune diseases: is it worth doing?2019 | 2. lékařská fakulta
- For Debate: The Significance of Etiologic Diagnosis in Neonates with Overgrowth Syndromes. Lesson Learned from the Simpson-Golabi-Behmel Syndrome2018 | Ústřední knihovna, 2. lékařská fakulta
- Short Stature in a Boy with Multiple Early-Onset Autoimmune Conditions due to a STAT3 Activating Mutation: Could Intracellular Growth Hormone Signalling Be Compromised?2017 | 2. lékařská fakulta
- MODY in Ukraine: genes, clinical phenotypes and treatment2017 | 2. lékařská fakulta
- Novel glucokinase gene mutation in the first Macedonian family tested for MODY2017 | 2. lékařská fakulta
Loading network view...