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Pregled prema Autor Koprivsek, Katarina M

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GodinaNaslovAutor(i)Tip rezultataMp-kat.
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, RainaNaučni članak
22M22 - Međunarodni časopis kategorije M22
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)Ostalo
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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, ZoranNaučni članak
23M23 - Međunarodni časopis kategorije M23
2024PNKP mutation in a child: is there a firm line between MCSZ and AOA4 phenotype?Semnic, Isidora; Ristic, Tamara; Koprivsek, Katarina MInformativni prilog
22M22 - Međunarodni časopis kategorije M22