Nina Bratanic
Ljubljana, Slovenia
Last Updated: 09/26/2026
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Found 11 publications
Familial Non-autoimmune Hyperthyroidism in Family Members Across Four Generations Due To a Novel Disease-causing Variant in The Thyrotropin Receptor Gene.
Journal: Balkan journal of medical genetics : BJMG
Published: April 05, 2021
Multifocal gastric adenocarcinoma in a patient with LRBA deficiency.
Journal: Orphanet journal of rare diseases
Published: March 30, 2017
IL-6-specific autoantibodies among APECED and thymoma patients.
Journal: Immunity, inflammation and disease
Published: February 29, 2016
Novel Mutations in HESX1 and PROP1 Genes in Combined Pituitary Hormone Deficiency.
Journal: Hormone research in paediatrics
Published: January 16, 2015
Childhood Osteoporosis and Presentation of Two Cases with Osteogenesis Imperfecta Type V.
Journal: Zdravstveno varstvo
Published: December 16, 2014
Clinical, Genetic and Immunological Characteristics of Paediatric Autoimmune Polyglandular Syndrome Type 1 Patients in Slovenia.
Journal: Zdravstveno varstvo
Published: October 27, 2014
Genetic risk for co-occurrence of type 1 diabetes and celiac disease is modified by HLA-C and killer immunoglobulin-like receptors.
Journal: Tissue antigens
Published: April 29, 2014
Improved metabolic control in pediatric patients with type 1 diabetes: a nationwide prospective 12-year time trends analysis.
Journal: Diabetes technology & therapeutics
Published: October 18, 2013
Anti-cytokine autoantibodies suggest pathogenetic links with autoimmune regulator deficiency in humans and mice.
Journal: Clinical and experimental immunology
Published: October 29, 2012
GAD65 antigen therapy in recently diagnosed type 1 diabetes mellitus.
Journal: The New England journal of medicine
Published: February 03, 2012
Showing 1-11 of 11
Last Updated: 09/26/2026