Damjan Osredkar

University of Ljubljana — SI

Medicine · Health Sciences

24h-index2.3kcitations135works1.62yr avg
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Research Topics

Neonatal and fetal brain pathology(37), Neonatal Respiratory Health Research(24), Neuroscience of respiration and sleep(15), Neurogenetic and Muscular Disorders Research(15), Thermal Regulation in Medicine(9)

Publications135 total

Prioritizing topics for a Clinical Practice Guideline on SATB2-Associated Syndrome: Methodological rigor versus clinical usability
Journal of Clinical Epidemiology·2026Open Access
Hydration and primary headaches in children and adolescents: a prospective interventional study
BMJ Nutrition Prevention & Health·2026Open Access
Endocrine and metabolic complications in a national cohort of Slovene children and adolescents with Duchenne muscular dystrophy
DiRROS repository (University of Maribor)·2026Open Access
Endocrine and metabolic complications in a national cohort of Slovene children and adolescents with Duchenne muscular dystrophy: real-world criteria for transition to vamorolone therapy
Frontiers in Endocrinology·2025Open Access
MSR177 Qualitative Analysis of Results From a Delphi Study to Formalize a Treatment Protocol for Children With Early Diagnosed Duchenne Muscular Disease (DMD) Using Giles®, an Artificial Intelligence Agent for Healthcare Research
Value in Health·2025
178PTwo-year stride-level evaluation of ambulatory function in ambulant DMD patients above 4 years old
Neuromuscular Disorders·2025
177PLongitudinal stride-level evaluation of ambulatory function with ankle wearable technology in ambulant DMD patients below 4 years old
Neuromuscular Disorders·2025
An evolutionarily conserved role for CTNNB1/β-CATENIN in regulating the development of the corpus callosum
iScience·2025· 2 citedOpen Access
Unravelling genetic etiology of cerebral palsy: findings from a Slovenian pediatric cohort
Frontiers in Neurology·2025Open Access
Genotypic, functional, and phenotypic characterization in CTNNB1 neurodevelopmental syndrome
Human Genetics and Genomics Advances·2025· 3 citedOpen Access
Gene therapy of rare diseases as a milestone in medicine - overview of the field and report on initial experiences in Slovenia
Orphanet Journal of Rare Diseases·2025· 2 citedOpen Access
Eculizumab for Thrombotic Microangiopathy Induced by Onasemnogene Abeparvovec in Spinal Muscular Atrophy
Case Reports in Nephrology and Dialysis·2025Open Access
Proteomic analysis identifying proteins relevant for treatment success following experimental neonatal inflammation-sensitized hypoxia-ischemia
Pediatric Research·2025· 1 citedOpen Access
Risks of Unregulated Home-Made Cannabis Products Used by Parents to Treat Refractory Epilepsy in Their Children
2025Open Access
Corrigendum: Diagnostic Approach to Children with Unexplained Global Developmental Delay in Pediatric Neurology Outpatient Clinic
Neuropediatrics·2025Open Access
Paving the way toward treatment solutions for CTNNB1 syndrome: a patient organization perspective
Therapeutic Advances in Rare Disease·2025· 3 citedOpen Access
Plant-derived cannabinoids for treatment of spasticity in children and adolescents with severe cerebral palsy: Double-blind, placebo-controlled trial
European Journal of Paediatric Neurology·2024· 4 cited
Newborn screening programs for spinal muscular atrophy worldwide in 2023
Journal of Neuromuscular Diseases·2024· 21 citedOpen Access
Diagnostic Approach to Children with Unexplained Global Developmental Delay in Pediatric Neurology Outpatient Clinic
Neuropediatrics·2024Open Access
400P Longitudinal evaluation of ambulatory function with ankle wearable technology in ambulant DMD
Neuromuscular Disorders·2024Open Access
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Frequent Co-authors

Marianne Thoresen(12), Elke Maes(9), David Neubauer(9), Hemmen Sabir(8), Thomas R. Wood(7), Mari Falck(7), Tadej Debevec(7), Grégoire P. Millet(7), Torun Flatebø(6), Tanja Golli(4), Minca Mramor(4), Anja Troha Gergeli(4), Alexander C. van Huffelen(3), Floris Groenendaal(3), Lars Walløe(3), Tita Butenko(3), Tanja Loboda(3), Mirjana Perković Benedik(3), Vincent Pialoux(3), Agnès Martin(3)