Marina Andjelkovic

5PUBLICATIONS
22CO-AUTHORS
Gene expression (incl. microarray and other genome-wide approaches)Neurology and neuromuscular diseasesInfant and child healthCell development, proliferation and death
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Publications (5)

|Sep 09, 2026
Costello Syndrome Associated With Somatic Mosaicism of Rare p.Gly13Asp HRAS Variant: Expanding the Phenotypic Spectrum.

|Aug 26, 2026
The Diagnostic Journey from Rhabdomyolysis to Myopathy with Tubular Aggregates: A Family-Based Case Report and Review of the Literature.

|May 26, 2026
RHOBTB2-Associated Neurological Phenotypes and Underlying Mechanisms: Alternating Hemiplegia of Childhood Beyond ATP1A3.

|May 13, 2026
Neuromuscular Disorders in Children Through the Lens of Next-Generation Sequencing: A Study of Diagnostic Yield.

|Jan 13, 2025
Phenylbutyric Acid Modulates Apoptosis and ER Stress-Related Gene Expression in Glycogen Storage Disease Type Ib In Vitro Model.

Marina Parezanovic, Nina Stevanovic, Marina Andjelkovic

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Frequent Collaborators

2 joint publications

Slavica Ostojić

2 joint publications

Gordana Kovačević

2 joint publications

Kristel Klaassen Ljubičić

2 joint publications

Anita Skakic