Stefan Blazina
Ljubljana, Slovenia
Last Updated: 09/26/2026
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Found 8 publications
The spectrum of clinical presentation in haploinsufficiency of A20; a case report of a novel mutation in TNFAIP3 gene.
Journal: Frontiers in pediatrics
Published: December 27, 2022
Flow Cytometric Determination of Actin Polymerization in Peripheral Blood Leukocytes Effectively Discriminate Patients With Homozygous Mutation in ARPC1B From Asymptomatic Carriers and Normal Controls.
Journal: Frontiers in immunology
Published: March 14, 2019
Vaccination coverage in children with rheumatic diseases.
Journal: Clinical and experimental rheumatology
Published: January 27, 2019
The role of IL-1 inhibition in systemic juvenile idiopathic arthritis: current status and future perspectives.
Journal: Drug design, development and therapy
Published: June 21, 2018
Functional Complement Analysis Can Predict Genetic Testing Results and Long-Term Outcome in Patients With Complement Deficiencies.
Journal: Frontiers in immunology
Published: January 16, 2018
Management of Juvenile Idiopathic Arthritis: A Clinical Guide.
Journal: Paediatric drugs
Published: August 04, 2016
Autoimmune and Inflammatory Manifestations in 247 Patients with Primary Immunodeficiency-a Report from the Slovenian National Registry.
Journal: Journal of clinical immunology
Published: February 22, 2016
11q terminal deletion and combined immunodeficiency (Jacobsen syndrome): Case report and literature review on immunodeficiency in Jacobsen syndrome.
Journal: American journal of medical genetics. Part A
Published: May 05, 2015
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Last Updated: 09/26/2026