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
- Small children's atlas of Endocrinology2013 | Third Faculty of Medicine, Second Faculty of Medicine
- 45,X/46,X,psu dic(Y) Gonadal Dysgenesis: Influence of the Two Cell Lines on the Clinical Phenotype, Including Gonadal Histology2013 | Second Faculty of Medicine
- 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
- High prevalence of coeliac disease in siblings of children with type 1 diabetes2005 | Third Faculty of Medicine, Second Faculty of Medicine, First Faculty of Medicine, Faculty of Physical Education and Sport
- Immune system in adults with childhood-onset growth hormone deficiency: effect of growth hormone therapy2000 | Third Faculty of Medicine, Second Faculty of Medicine
- Děti, které málo rostou - dělení z aspektu etiologie1997 | Second Faculty of Medicine
- NPHP3-Related Disease: A Possible Risk Factor for Developing Encapsulating Peritoneal Sclerosis2024 | Second Faculty of Medicine
- The genetic landscape of children born small for gestational age with persistent short stature (SGA-SS)2024 | Second Faculty of Medicine
- Integrative role of the SALL4 gene: From thalidomide embryopathy to genetic defects of the upper limb, internal organs, cerebral midline, and pituitary2024 | Second Faculty of Medicine
- SALL4 phenotype in four generations of one family: An interplay of the upper limb, kidneys, and the pituitary2024 | Second Faculty of Medicine
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