- How can genetic investigation contribute to choice of proper treatment of diabetic patient2010 | Second Faculty of Medicine
- De novo mutations of GCK, HNF1A and HNF4A may be more frequent in MODY than previously assumed2014 | Second Faculty of Medicine, First Faculty of Medicine, Faculty of Physical Education and Sport
- The Common p.R114W HNF4A Mutation Causes a Distinct Clinical Subtype of Monogenic Diabetes2016 | Second Faculty of Medicine
- A novel-192c/g mutation in the proximal P2 promoter of the hepatocyte nuclear factor-4 alpha gene (HNF4A) associates with late-onset diabetes2006 | Third Faculty of Medicine, Second Faculty of Medicine
- Lack of PAX4 mutations in 53 Czech MODYX families2010 | Second Faculty of Medicine
- Half-Life of Sulfonylureas in HNF1A and HNF4A Human MODY Patients is not Prolonged as Suggested by the Mouse Hnf1a(-/-) Model2015 | Third Faculty of Medicine
- Association of birthweight and penetrance of diabetes in individuals with HNF4A-MODY: a cohort study2022 | Second Faculty of Medicine
- Best practice guidelines for the molecular genetic diagnosis of maturity-onset diabetes of the young2008 | Second Faculty of Medicine
- HNF1A mutation presenting with fetal macrosomia and hypoglycemia in childhood prior to onset of overt diabetes +12011 | Third Faculty of Medicine, Second Faculty of Medicine
- Hepatocyte nuclear factors and diabetes mellitus2017 | Third Faculty of Medicine
- Congenital hyperinsulinism: Loss of B-cell self-control2016 | Second Faculty of Medicine
- MODY in Ukraine: genes, clinical phenotypes and treatment2017 | Second Faculty of Medicine
- Target genes, variants, tissues and transcriptional pathways influencing human serum urate levels2019 | First Faculty of Medicine
- Hypoglycemia and antihyperglycemic treatment in adult MODY patients - A systematic review of literature2019 | Third Faculty of Medicine, Second Faculty of Medicine
- Aetiological heterogeneity of asymptomatic hyperglycaemia in children and adolescents2006 | Third Faculty of Medicine, Second Faculty of Medicine
- High incidence of heterozygous ABCC8 and HNF1A mutations in Czech patients with congenital hyperinsulinism2015 | Third Faculty of Medicine, Second Faculty of Medicine, First Faculty of Medicine
- Three novel mutations in MODY and its phenotype in three different Czech families2010 | Faculty of Medicine in Pilsen, Third Faculty of Medicine
- The Diagnosis and Management of Hyperinsulinaemic Hypoglycaemia2015 | Second Faculty of Medicine
- Expression Profiling of Nme7 Interactome in Experimental Models of Metabolic Syndrome2018 | First Faculty of Medicine
- Autoantibodies against ZnT8 are rare in Central-European LADA patients and absent in MODY patients, including those positive for other autoantibodies2019 | Third Faculty of Medicine
- Substantial proportion of MODY among multiplex families participating in a Type 1 diabetes prediction programme2016 | Second Faculty of Medicine
- Hidden MODY-Looking for a Needle in a Haystack2018 | Third Faculty of Medicine, Second Faculty of Medicine
- Heterogeneity of gestational diabetes - Do we take MODY into consideration as much as we should?2019 | Third Faculty of Medicine, Second Faculty of Medicine
