Romana Juraski-Gjergja
Zagreb, Croatia
Last Updated: 09/26/2026
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Found 11 publications
Changes in General Movements During Early Intensive Rehabilitation in High-Risk Infants with Structural Brain Injury: A Preliminary Study.
Journal: Children (Basel, Switzerland)
Published: March 17, 2026
Personalized music improves epileptiform activity, REM sleep and quality of life in children with epilepsies.
Journal: Epilepsy & behavior : E&B
Published: December 20, 2025
Respiratory Syncytial Virus-Specific Antibodies and Atopic Diseases in Children: A 10-Year Follow-Up.
Journal: Pathogens (Basel, Switzerland)
Published: January 30, 2023
Respiratory syncytial virus specific immunoglobulin G4 antibodies and atopic diseases in children.
Journal: Minerva pediatrics
Published: February 15, 2022
Fetal Cystic Hygroma Associated with Terminal 2p25.1 Duplication and Terminal 3p25.3 Deletion: Cytogenetic, Fluorescent in Situ Hybridization and Microarray Familial Characterization of Two Different Chromosomal Structural Rearrangements.
Journal: Balkan journal of medical genetics : BJMG
Published: April 05, 2021
Sources of variability in expiratory flow profiles during sleep in healthy young children.
Journal: Respiratory physiology & neurobiology
Published: September 17, 2019
Missense Mutations of the Pro65 Residue of PCGF2 Cause a Recognizable Syndrome Associated with Craniofacial, Neurological, Cardiovascular, and Skeletal Features.
Journal: American journal of human genetics
Published: December 12, 2018
Overnight Video-Polysomnographic Studies in Children with Intractable Epileptic Encephalopathies.
Journal: Medical science monitor : international medical journal of experimental and clinical research
Published: August 05, 2018
Missense Mutations of the Pro65 Residue of PCGF2 Cause a Recognizable Syndrome Associated with Craniofacial, Neurological, Cardiovascular, and Skeletal Features.
Journal: American journal of human genetics
Published: May 16, 2018
The Croatian Model of Integrative Prospective Management of Epilepsy and Pregnancy
Journal: Acta clinica Croatica
Published: November 09, 2017
Prenatal diagnosis of complex phenotype in a 13-week-old fetus with an interstitial multigene deletion 20q13.13.-q13.2 by chromosomal microarray.
Journal: European journal of medical genetics
Published: January 21, 2017
Showing 1-11 of 11
Last Updated: 09/26/2026