Study programme
Classes
- Molecular pathogenesis and therapy of paediatric endocrine disordersD0100020 | Second Faculty of Medicine
- Transplantation and gene therapy +1D0100027 | 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
- Water and Electrolytes Distubances in Children +1D0100026 | 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
Publications
- 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
- 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
- Contemporary indications for growth hormone therapy in paediatrics2005 | Second Faculty of Medicine, Central Library of Charles University
- The uterine length in women with Turner syndrome reflects the postmenarcheal daily estrogen dose2003 | Third Faculty of Medicine, Second Faculty of Medicine
- IGF-I Resistance and Turner's Syndrome2001 | Third Faculty of Medicine, Second Faculty of Medicine
- Immune system in adults with childhood-onset growth hormone deficiency: effect of growth hormone therapy2000 | Third Faculty of Medicine, 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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