Study programme
Classes
- Transplantation ?????D01000152 | Second Faculty of Medicine
- Molecular pathogenesis and therapy of paediatric endocrine disordersD0100020 | Second Faculty of Medicine
- Water and Electrolytes Distubances in Children +1D0100026 | Second Faculty of Medicine
- Transplantation and gene therapy +1D0100027 | Second Faculty of Medicine
- Selected case studies and best practices in pediatricsD0100029 | Second Faculty of Medicine
- Nutrition the children in health and diseaseD0100030 | Second Faculty of Medicine
- Molecular microbiology - diagnostic principlesD0100066 | Second Faculty of Medicine
- Social Problems in PaediatricsD0100070 | Second Faculty of Medicine
- Paediatrics I +1D0108068 | Second Faculty of Medicine
- Clinical 10 days - Department of Paediatrics +1D0110PED | Second Faculty of Medicine
Publications
- Two Cases of Diabetic Ketoacidosis in HNF1A-MODY Linked to Severe Dehydration: Is it time to change the diagnostic criteria for MODY?2013 | Second Faculty of Medicine, First Faculty of Medicine, Faculty of Physical Education and Sport, Faculty of Medicine in Hradec Králové
- Chronic Mild Hyperglycemia in GCK-MODY Patients Does Not Increase Carotid Intima-Media Thickness2013 | Third Faculty of Medicine, Second Faculty of Medicine, Faculty of Mathematics and Physics
- Treatment Options for Children with Monogenic Forms of Obesity2013 | Third Faculty of Medicine, Second Faculty of Medicine
- Impaired Growth during Childhood in Patients with Primary Ciliary Dyskinesia2013 | Second Faculty of Medicine
- Rituximab resistant evans syndrome and autoimmunity in Schimke immuno-osseous dysplasia2011 | Second Faculty of Medicine, First Faculty of Medicine, Faculty of Physical Education and Sport, Faculty of Medicine in Hradec Králové
- Unusually severe phenotype of neonatal primary hyperparathyroidism due to a heterozygous inactivating mutation in the CASR gene2009 | Second Faculty of Medicine, First Faculty of Medicine, Faculty of Physical Education and Sport
- Pituitary Morphology in Patients with Combined Pituitary Hormone Deficiency Due to PROP1 Gene Mutations2005 | Third Faculty of Medicine, First Faculty of Medicine, Faculty of Physical Education and Sport
- Auxological and endocrine phenotype in a population-based cohort of patients with PROP1 gene defects2005 | Third Faculty of Medicine, First Faculty of Medicine, Faculty of Physical Education and Sport
- MODY diabetes in the Czech republic: Identification of a new gene mutations for HNF-1alfa, HNF-4alfa and glucokinasePublication without faculty affiliation
- NPHP3-Related Disease: A Possible Risk Factor for Developing Encapsulating Peritoneal Sclerosis2024 | Second Faculty of Medicine
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