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Slika profila

Bernarda Lozić

31699

Bernarda

Lozić

izv. prof. dr. sc.

Naziv Uloga Akcije
Genetska dijagnostika malformacija bubrega i mokraćnog sustava suradnik
Naziv Akcije
Batel, Anja ; Polović, Mirjana ; Glumac, Mateo; Šuman, Oliver; Jadrijević, Stipislav; Lozić, Bernarda; Petrović, Marija; Samardžija, Bobana; Bradshaw, Nicholas J; Skube, Karlo et al. SPRTN is involved in hepatocellular carcinoma development through the ER stress response // Cancer gene therapy, (2023), doi: 10.1038/s41417-023-00708-w
Šmaguc, Ana ; Petković Ramadža, Danijela ; Sarnavka, Vladimir ; Krželj, Vjekoslav ; Lozić, Bernarda ; Pušeljić, Silvija ; Rahelić, Valentina ; Mesarić, Nikola ; Grubić, Marina ; Bogdanić, Ana et al. Iskustva s galaktozemijom u Hrvatskoj // Liječnički vjesnik : glasilo Hrvatskoga liječničkog zbora, 145 (2023), 1-2; 1-11. doi: 10.26800/LV-145-1-2-1
Visković Veljačić, Daniela ; Lozić, Mirela ; Vukoja, Martina ; Šoljić, Violeta ; Vukojević, Katarina ; Glavina Durdov, Merica ; Filipović, Natalija ; Lozić, Bernarda Spatio-Temporal Expression Pattern of CAKUT Candidate Genes DLG1 and KIF12 during Human Kidney Development // Biomolecules, 13 (2023), 2; 340, 19. doi: 10.3390/biom13020340
Batinović, Ena ; Papazovska Cherepnalkovski, Anet ; Lozić, Bernarda ; Brajković, Luka ; Zanchi, Ivana ; Pavlov, Vesna ; Bucat, Marija First Croatian Case of Double Aneuploidy: A Child With Klinefelter and Edwards Syndrome (48,XXY,+18) – Possible Causes and Contributing Factors // Acta Medica (Hradec Kralove), 66 (2023), 1; 32-36. doi: 10.14712/18059694.2023.13
Blažeković, Antonela ; Gotovac Jerčić, Kristina ; Meglaj, Sarah ; Đuranović, Vlasta ; Prpić, Igor ; Lozić, Bernarda ; Malenica, Maša ; Markovic, Silvana ; Lujić, Lucija ; Petelin Gadže, Željka et al. Genetics of Pediatric Epilepsy: Next-Generation Sequencing in Clinical Practice // Genes, 13 (2022), 8; 1466, 10. doi: 10.3390/genes13081466
Simičić Majce, Ana ; Arapović, Adela ; Prgomet, Sandra ; Todorović, Marko ; Lozić, Bernarda ; Saraga- Babić, Mirna ; Sarga, Marijan Bardet-Biedl syndrome caused by compound heterozygosity of BBS12 gene in one family: a case report. In: Abstracts of the 54th ESPN Annual Meeting, Ljubljana, Slovenia. // Pediatric Nephrology. 2022. str. 2937-2937 doi: 10.1007/s00467-022-05680-5
Runjic, Edita ; Jelicic Kadic, Antonia ; Bastian, Lorenz ; Lozic, Mirela ; Buljubasic Soda, Maja ; Petrovic, Marija ; Malic Tudor, Karolina ; Kuljis, Dubravka ; Armanda, Visnja ; Lozic, Bernarda Clinical and Cytogenetic Characteristics of Children With Leukemia 20-Year Retrospective Study // Journal of pediatric hematology/oncology, (2022), 1-20. doi: 10.1097/mph.0000000000002529
Kovačević, Tanja ; Polić, Branka ; Markić, Joško ; Ardalić Ćatipović, Tatjana ; Bucat, Marija ; Mikulić, Svjetlana ; Žuvan, Leona ; Pogorelić, Zenon ; Despot, Ranka ; Žitko, Vanda et al. Treatment outcomes in neonates with esophageal atresia: a 30-year single-center experience // Zbornik radova / Konstantinidis, Geogrios (ur.). Novi Sad: Udruženje pedijatara Srbije, 2022. str. 77-77
Kunac, Nenad ; Bezić, Joško ; Vuko, Arijana ; Bašić, Željana ; Jerković, Ivan ; Kružić, Ivana ; Ljubić, Toni ; Lozić, Bernarda ; Sardelić, Sanda ; Anđelinović, Šimun Building the COVID-19 Testing Capacities in Croatia: Establishing the Interdepartmental COVID-19 Unit at the Split University Hospital Centre // Acta clinica Croatica, 60 (2021), 2; 254-258. doi: 10.20471/acc.2021.60.02.11
Kloth, Katja ; Lozic, Bernarda ; Tagoe, Julia ; Hoffer, Mariëtte J V ; Van der Ven, Amelie ; Thiele, Holger ; Altmüller, Janine ; Kubisch, Christian ; Au, Ping Yee Billie ; Denecke, Jonas et al. ANK3 related neurodevelopmental disorders: expanding the spectrum of heterozygous loss-of- function variants // Neurogenetics, 22 (2021), 4; 263-269. doi: 10.1007/s10048-021-00655-4
nije evidentirano
nije evidentirano