Aneta Soltirovska-Šalamon

6PUBLICATIONS
16CO-AUTHORS
Infant and child healthNeurogeneticsCentral nervous systemEpigenetics (incl. genome methylation and epigenomics)Respiratory diseases
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Publications (6)

|Jul 24, 2026
Universal Dried Blood Spot Screening for Congenital Cytomegalovirus: A Slovenian National Implementation Pilot.

|Apr 22, 2026
Tubulinopathy Case Series: Marked Intrafamilial Phenotypic Variability Associated With a Novel Missense TUBB Variant.

|Jul 27, 2024
Diagnostics of Metabolic Bone Disease in Extremely Preterm Infants-Clinical Applicability of Bone Turnover Biochemical Markers and Quantitative Ultrasound.

Sandra Cerar, Lara Vurzer, Aneta Soltirovska Šalamon

|Jul 06, 2023
EEG functional connectivity after perinatal stroke.

Alja Kavčič, Jure Demšar, Dejan Georgiev

|Sep 28, 2021
Genetic Polymorphisms, Gene-Gene Interactions and Neurologic Sequelae at Two Years Follow-Up in Newborns with Hypoxic-Ischemic Encephalopathy Treated with Hypothermia.

Katarina Esih, Katja Goričar, Aneta Soltirovska-Šalamon

|Jan 15, 2021
CARD8 and IL1B Polymorphisms Influence MRI Brain Patterns in Newborns with Hypoxic-Ischemic Encephalopathy Treated with Hypothermia.

Katarina Esih, Katja Goričar, Zvonka Rener-Primec

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Frequent Collaborators

2 joint publications

Alja Kavčič

1 joint publications

Jure Demšar

1 joint publications

Dejan Georgiev

1 joint publications

Nuška Pečarič Meglič