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
- Prepubertal Girls With Turner Syndrome and Children With Isolated SHOX Deficiency Have Similar Bone Geometry at the Radius2013 | Second Faculty of Medicine, First Faculty of Medicine, Faculty of Mathematics and Physics, Faculty of Science
- 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
- Boys with haemophilia have low trabecular bone mineral density and sarcopenia, but normal bone strength at the radius2012 | Second Faculty of Medicine, Faculty of Mathematics and Physics, Faculty of Science
- 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
- 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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