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Browsing by Author Koprivsek, Katarina M

Showing results 1 to 5 of 5
Issue DateTitleAuthor(s)TypeМp-cat.
20253-Hydroxy-3-methylglutaryl-coenzyme A lyase deficiency: case report of a child with rare HMGCL gene variantsBjelica, Milena; Stojadinovic, Aleksandra; Knezevic-Pogancev, Marija F; Koprivsek, Katarina M; Sass, Jorn Oliver; Gruenert, Sarah C; Wuensche, Falko; Yamamoto, RainaArticle
22M22
2004Bilateral chorea-ballism associated with hyperthyroidismRistic, Aleksandar J  ; Svetel, Marina V ; Dragasevic, Natasa T; Zarkovic, Milos P  ; Koprivsek, Katarina M; Kostic, Vladimir SNaučni članak
21M21 - Vodeći međunarodni časopis kategorije M21
2020Clinical and genetic landscape of treatment naive cervical cancer: Alterations in PIK3CA and in epigenetic modulators associated with sub-optimal outcome (vol 43, pg 253, 2019)Scholl, Suzy M; Popovic, Marina; ...; Mandic, Aljosa D  ; Koprivsek, Katarina M; ...; Malenkovic, Goran; Djuran, Branislav; ...; (broj, koautora 54)Other
Mp. category will be shown later
2011Partial rhombencephalosynapsis: prenatal MR imaging diagnosis and postnatal follow upKoprivsek, Katarina M; Novakov-Mikic, Aleksandra S; Lucic, Milos A; Kozic, Dusko B  ; Till, Viktor E; Belopavlovic, ZoranArticle
23M23
2024PNKP mutation in a child: is there a firm line between MCSZ and AOA4 phenotype?Semnic, Isidora; Ristic, Tamara; Koprivsek, Katarina MContribution to periodical
22M22