Publications
- Functional Analyses of HNF1A-MODY Variants Refine the Interpretation of Identified Sequence Variants2020 | Second Faculty of Medicine
- NPR2 Variants Are Frequent among Children with Familiar Short Stature and Respond Well to Growth Hormone Therapy2020 | Second Faculty of Medicine
- Short stature in a boy with atypical progeria syndrome due to LMNA c.433G>A [p.(Glu145Lys)]: Apparent growth hormone deficiency but poor response to growth hormone therapy2019 | Second Faculty of Medicine
- High Prevalence of Growth Plate Gene Variants in Children With Familial Short Stature Treated With GH2019 | Second Faculty of Medicine
- Screening of monogenic autoimmune diabetes among children with type 1 diabetes and multiple autoimmune diseases: is it worth doing?2019 | Second Faculty of Medicine
- MODY in Ukraine: genes, clinical phenotypes and treatment2017 | Second Faculty of Medicine
- Combined pituitary hormone deficiency due to gross deletions in the POU1F1 (PIT-1) and PROP1 genes2017 | Second Faculty of Medicine
- Genesis of two most prevalent PROP1 gene variants causing combined pituitary hormone deficiency in 21 populations2016 | Second Faculty of Medicine
- The Common p.R114W HNF4A Mutation Causes a Distinct Clinical Subtype of Monogenic Diabetes2016 | Second Faculty of Medicine
- Hepatic phenotypes of HNF1B gene mutations: A case of neonatal cholestasis requiring portoenterostomy and literature review2015 | Second Faculty of Medicine, First Faculty of Medicine, Faculty of Physical Education and Sport
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