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Aneta Soltirovska-Šalamon

5PUBLICATIONS

12CO-AUTHORS

NeurogeneticsInfant and child healthCentral nervous systemEpigenetics (incl. genome methylation and epigenomics)Respiratory diseases

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Publications (5)

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|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

<i>CARD8</i> and <i>IL1B</i> 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

1 joint publications

Sandra Cerar

1 joint publications

Tina Perme

1 joint publications

Adrijana Oblak

1 joint publications

Štefan Grosek

1 joint publications

Katarina Esih

1 joint publications

Katja Goričar

Frequent Collaborators

2 joint publications

Alja Kavčič

1 joint publications

Jure Demšar

1 joint publications

Dejan Georgiev

1 joint publications

Nuška Pečarič Meglič

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