|
|
3. Variants in the circadian clock genes PER2 and PER3 associate with familial sleep phase disordersLaura Plavc, Cene Skubic, Leja Dolenc-Grošelj, Damjana Rozman, 2024, original scientific article Keywords: circadian clock, genetics, PER2, sleep phase disorders, genotyping, PER3 Full text (file, 2,15 MB) This document has more files! More... |
4. A clinical perspective on imaging in juvenile idiopathic arthritisMaria Tarsia, Mojca Zajc Avramovič, Ana Gazikalović, Damjana Ključevšek, Tadej Avčin, 2024, review article Keywords: children, conventional radiography, imaging, juvenile idiopathic arthritis, magnetic resonance imaging, ultrasound Full text (file, 2,33 MB) This document has more files! More... |
5. Biparietal remodelling and total vault remodelling in scaphocephaly—a comparative study using 3d stereophotogrammetryPeter Spazzapan, Miha Verdenik, Tomaž Velnar, 2024, original scientific article Keywords: biparietal remodelling, comparative study, stereophotogrammetry, scaphocephaly, 3D stereophotogrammetry, craniosynostosis, cranial index Full text (file, 1,46 MB) This document has more files! More... |
6. Učinki elektrokemoterapije in ionizirajočega sevanja na imunološko pomembne spremembe v tumorskih celicahUrša Kešar, 2024, doctoral dissertation Keywords: Elektrokemoterapija, ionizirajoče sevanje, cisplatin, oksaliplatin, bleomicin, imunogena celična smrt, ATP, HMGB1, kalretikulin, MHC I, MHC II, PD-L1, CD40 Full text (file, 4,76 MB) |
7. Gestational diabetes perception profiles based on attachment styleAna Munda, Katarina Kompan Erzar, Helena Perić, Draženka Pongrac Barlovič, 2024, original scientific article Keywords: gestational diabetes, illness perception, attachment styles, latent profile analysis, disease burden Full text (file, 656,45 KB) This document has more files! More... |
8. Morphological and functional correlations in acute central serous chorioretinopathyPeter Kiraly, Maja Šuštar Habjan, Jaka Smrekar, Polona Jaki Mekjavić, 2024, original scientific article Keywords: central serous chorioretinopathy, CSC, CSR, correlations, morphological correlations, functional correlations Full text (file, 840,55 KB) This document has more files! More... |
9. The CC2D2B is a novel genetic modifier of the clinical phenotype in patients with hereditary angioedema due to C1 inhibitor deficiencyNina Rupar, Julij Šelb, Mitja Košnik, Mihaela Zidarn, Slađana Andrejević, Ljerka Čulav, Vesna Grivčeva-Panovska, Peter Korošec, Matija Rijavec, 2024, original scientific article Keywords: hereditary angioedema, C1 inhibitor deficiency, genetic modifiers, clinical phenotype, genotype-phenotype correlation, genetic variant, SERPING1, CC2D2B Full text (file, 4,80 MB) This document has more files! More... |
|