Study programme
Classes
- Molecular pathogenesis and therapy of paediatric endocrine disordersD0100020 | Second Faculty of Medicine
- Water and Electrolytes Distubances in Children +1D0100026 | Second Faculty of Medicine
- Selected case studies and best practices in pediatricsD0100029 | Second Faculty of Medicine
- OS - Molecular pathogenesis and therapy of paediatrics endocrine disordersDV01020 | Second Faculty of Medicine
- OS - Molecular pathogenesis and therapy of paediatric endocrine disordersDVA1020 | Second Faculty of Medicine
- Transplantation ?????D01000152 | Second Faculty of Medicine
- Transplantation and gene therapy +1D0100027 | 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
Publications
- Contemporary indications for growth hormone therapy in paediatrics2005 | Second Faculty of Medicine, Central Library of Charles University
- Metabolic Compensation of Diabetic Children: Study Edmonton - Prague 1993 - 19992000 | Third Faculty of Medicine, Second Faculty of Medicine
- Late sequelae of complex anti-tumourous treatment in children and adolescents with solid extracranial tumours: Effect on growth, pubertal development and gonadal function1997 | Second Faculty of Medicine, Central Library of Charles University
- Brain edema during the treatment of enuresis with Audiretin1997 | Second Faculty of Medicine
- Impairedd growth and development - late sequelae ofd complex anti-tumorous treatment of children and adolescents with primary brain tumours distant from the midline1997 | 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
- Paediatric diabetes subtypes in a consanguineous population: a single-centre cohort study from Kurdistan, Iraq2024 | Second Faculty of Medicine
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