Skip to main content

ETHNOS_APP

Home • Search • Journals • List 0

Ognjen Ležakov

Biographic Data

ID8264281
NAMEOgnjen Ležakov
GIVEN NAMESOgnjen
FAMILY NAMELežakov
SIGNATURELEŽAKOV O
AFFILIATIONSUniversity of Novi Sad
ORCID0009-0007-0354-0458
VERIFIEDYes
TOTAL WORKS2
TOTAL CITATIONS0
WORKS AS AUTHOR2
WORKS AS EDITOR0
FIRST PUBLICATION YEAR2025
LATEST PUBLICATION YEAR2025
H-INDEX0
  • Sarcoidosis-like Skin Lesions as the First Manifestation of Ataxia-Telangiectasia

    Open Access•Borko Milanović, Gordana Vijatov-Djuric et al.•ARTICLE•Children•2025

    Ataxia-telangiectasia is a rare autosomal recessive disorder that is difficult to diagnose due to its unpredictable presentation. It is characterized by cerebellar degeneration, telangiectasias, immunodeficiency, frequent pulmonary infections, and tumors. Immune system abnormalities manifest as disruptions in both cellular and humoral immunity. The most common findings include decreased levels of immunoglobulin classes (IgA, IgM, IgG, and IgG sub…

  • TPMT and HLA-DQ Allelic Variants in Relation to Drug Response, Safety and Need for Therapy Optimization in Pediatric Inflammatory Bowel Disease

    Open Access•M Stojsić, Ognjen Ležakov et al.•ARTICLE•Children•2025

    Prior to the initiation of azathioprine therapy, TPMT genotyping should be performed to prevent adverse effects and ensure optimal drug dosing. Identification of the HLA-DQA105 and HLA-DQA101 alleles plays an important role in the planning of biological therapy regimens, including decisions on dose escalation or interval shortening

No prominent works on this page.

  • Sarcoidosis-like Skin Lesions as the First Manifestation of Ataxia-Telangiectasia

    Open Access•Borko Milanović, Gordana Vijatov-Djuric et al.•ARTICLE•Children•2025

    Ataxia-telangiectasia is a rare autosomal recessive disorder that is difficult to diagnose due to its unpredictable presentation. It is characterized by cerebellar degeneration, telangiectasias, immunodeficiency, frequent pulmonary infections, and tumors. Immune system abnormalities manifest as disruptions in both cellular and humoral immunity. The most common findings include decreased levels of immunoglobulin classes (IgA, IgM, IgG, and IgG sub…

  • TPMT and HLA-DQ Allelic Variants in Relation to Drug Response, Safety and Need for Therapy Optimization in Pediatric Inflammatory Bowel Disease

    Open Access•M Stojsić, Ognjen Ležakov et al.•ARTICLE•Children•2025

    Prior to the initiation of azathioprine therapy, TPMT genotyping should be performed to prevent adverse effects and ensure optimal drug dosing. Identification of the HLA-DQA105 and HLA-DQA101 alleles plays an important role in the planning of biological therapy regimens, including decisions on dose escalation or interval shortening

Adverse effect (1 work) · Allele (1 work) · Ataxia (1 work) · Ataxia-telangiectasia (1 work) · Autoimmune Neurological Disorders and Treatments (1 work) · Azathioprine (1 work) · Biology (1 work) · Dermatology (1 work) · Disease (1 work) · DNA Repair Mechanisms (1 work)

Ethnos_APP • Open Source Project • MIT License • Frontend v2.0.0 • Privacy and Cookies • API Documentation: api.ethnos.app/docs • API Source Code: GitHub • DOI: 10.5281/zenodo.17049435 • Frontend Source Code: GitHub • DOI: 10.5281/zenodo.17050053 • cruz.rio.br • Expectantes Misericordiae