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Croatian Medical Journal|May 4, 2022
Next-generation sequencing of von Willebrand factor and coagulation factor VIII genes: a cross-sectional study in Croatian adult patients diagnosed with von Willebrand diseaseIvana Lapić, Margareta Radić Antolic, Ana Boban, et al.Journal of Medical Virology|April 13, 2022
Association of polymorphisms in genes encoding prothrombotic and cardiovascular risk factors with disease severity in COVID-19 patients: A pilot studyIvana Lapić, Margareta Radić Antolic, Ivana Horvat, et al.Biochemia Medica|October 19, 2020
Urine neutrophil gelatinase-associated lipocalin concentration in healthy newborns during the first three postnatal daysVinka Mikulić, Dunja Rogić, Ivanka Mikulić, et al.Biochemia Medica|October 19, 2020
Verification of automated latex-enhanced particle immunoturbidimetric D-Dimer assays on different analytical platforms and comparability of test resultsIvana Lapić, Désirée Coen Herak, Snježana Prpić, et al.Archives of Medical Science : AMS|May 20, 2022
Influence of disease severity, smoking status and therapy regimes on leukocyte subsets and their ratios in stable chronic obstructive pulmonary diseaseIva Hlapčić, Andrea Vukić Dugac, Sanja Popović-Grle, et al.Diagnosis (Berlin, Germany)|July 7, 2025
Minimizing the discard blood volume from the central venous catheter for routine laboratory testing in adult intensive care unitIvana Lapić, Josipa Kostelac, Luka Bielen, et al.Medicina (Kaunas, Lithuania)|March 27, 2025
Interleukin-6 and Leukocyte Cell Population Data in Newly Diagnosed Sepsis-A Prospective StudySara Šundalić, Iva Košuta, Ivana Baršić Lapić, et al.Journal of Clinical Medicine|October 16, 2024
Early Fever in Allogeneic Stem Cell Transplantation: Are Presepsin and YKL-40 Valuable Diagnostic Tools?Jakša Babel, Iva Košuta, Ana Vujaklija Brajković, et al.Collegium Antropologicum|August 23, 2014
Peripheral arterial catheter related infections in the neurosurgical intensive care unitJelena Radonić, Ljiljana Mihaljević, Radovan Radonić, et al.Laboratory Medicine|December 5, 2022
Type 1 von Willebrand Disease in a Pediatric Patient Caused by a Novel Heterozygous Deletion of Exons 1 to 6 of the von Willebrand Factor Gene: A Case ReportIvana Lapić, Margareta Radić Antolic, Dunja Rogić, et al.Pageof 8