11. Novel GRHL2 gene variant associated with hearing lossKatarina Trebušak Podkrajšek, Tine Tesovnik, Nina Božanić Urbančič, Saba Battelino, 2021, review article Keywords: autosomal-dominant hearing loss, next-generation sequencing, NGS, GRHL2 gene Full text (file, 2,66 MB) This document has more files! More... |
12. Malignant syphilis in a female patientJulija Dimnik, Maja Benko, Violeta Hosta, Andreja Murnik-Rauh, Andreja Pagon, Vesna Špik, Saba Battelino, Domen Vozel, 2022, short scientific article Keywords: sexually transmitted diseases, syphilis serodiagnosis, otolaryngology, dermatology, diagnostic errors Full text (file, 2,18 MB) This document has more files! More... |
13. Autologous platelet and extracellular vesicle-rich plasma as therapeutic fluidKaja Troha, Domen Vozel, Matevž Arko, Apolonija Bedina Zavec, Drago Dolinar, Matej Hočevar, Zala Jan, Matic Kisovec, Boštjan Kocjančič, Ljubiša Pađen, Manca Pajnič, Samo Penič, Anna Romolo, Neža Repar, Vesna Spasovski, Nejc Steiner, Vid Šuštar, Aleš Iglič, Damjana Drobne, Ksenija Kogej, Saba Battelino, Veronika Kralj-Iglič, 2023, review article Keywords: platelet-rich plasma, platelets, centrifugation, extracellular vesicles, small cellular particles, wound healing, regeneration, fresh-frozen plasma, intercellular signaling peptides and proteins Full text (file, 2,37 MB) This document has more files! More... |
14. Unraveling the etiology of pediatric vertigo and dizzinessNina Božanić Urbančič, Domen Vozel, Jure Urbančič, Saba Battelino, 2021, original scientific article Keywords: Lyme neuroborreliosis, adolescent, child, dizziness, vertigo, migraine disorders, interdisciplinary communication, headache, medulloblastoma, somatoform disorders Full text (file, 1,47 MB) This document has more files! More... |
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17. Double hyperautofluorescent rings in patients with USH2A-retinopathyAna Fakin, Maja Šuštar Habjan, Jelka Brecelj, Crystel Bonnet, Christine Petit, Andrej Zupan, Damjan Glavač, Martina Jarc-Vidmar, Saba Battelino, Marko Hawlina, 2019, original scientific article Keywords: USH2A-retinopathy, double hyperautofluorescent rings, electrophysiology, USH2A, usher syndrome, retinitis pigmentosa, fundus autofluorescence, cone-rod dystrophy Full text (file, 5,19 MB) This document has more files! More... |
18. The importance of early genetic diagnostics of hearing loss in childrenNina Božanić Urbančič, Saba Battelino, Tine Tesovnik, Katarina Trebušak Podkrajšek, 2020, review article Keywords: hearing loss, children, genetic diagnostics, genetic testing, etiology, benefits, health, family Full text (file, 1,09 MB) This document has more files! More... |
19. Applicability of platelet- and extracellular vesicle-rich plasma in medicineDomen Vozel, Marko Jeran, Darja Božič, Ljubiša Pađen, Manca Pajnič, Bojana Uršič, Veronika Kralj-Iglič, Saba Battelino, 2019, published scientific conference contribution Keywords: platelets, platelet-rich plasma, extracellular vesicles, regenerative effects, haemostasis, immune response, blood immune cells Full text (file, 328,50 KB) |
20. Dataset on amelogenesis-related genes variants (ENAM and ENAM interacting genes) and on human leukocyte antigen alleles (DQ2 and DQ8) distribution in children with and without molar–incisor hypomineralisation (MIH)Luka Hočevar, Jernej Kovač, Katarina Trebušak Podkrajšek, Saba Battelino, Alenka Pavlič, 2020, original scientific article Keywords: amelogenesis, molar–incisor hypomineralisation, MIH, genes variants, aetiology, human leukocyte antigen, amelogenesis-related genes, single nucleotide polymorphism Full text (file, 759,06 KB) This document has more files! More... |