Publications
- Short Stature in a Boy with Multiple Early-Onset Autoimmune Conditions due to a STAT3 Activating Mutation: Could Intracellular Growth Hormone Signalling Be Compromised?2017 | 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
- High Prevalence of PROP1 Defects in Lithuania: Phenotypic Findings in an Ethnically Homogenous Cohort of Patients With Multiple Pituitary Hormone Deficiency2014 | Second Faculty of Medicine
- Is genetic testing in children with growth hormone deficiency clinically justified?2013 | 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
- Lucas who likes horses2011 | Second Faculty of Medicine
- Mutations and Pituitary Morphology in a Series of 82 Patients with PROP1 Gene Defects2011 | Second Faculty of Medicine
- Clinical Importance of Identification of PROP1 Gene Mutations in Children with Inherited Growth Hormone Deficiency2009 | Second Faculty of Medicine
- Calcium-sensing receptor: Physiology and conditions connected with its disorders2009 | Second Faculty of Medicine
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