Results 1-5 of 5
Issue DateTitleAuthor(s)TypeМp-cat.
2024Whole exome sequencing in Serbian patients with hereditary spastic paraplegiaBranković, Marija  ; Ivanović, Vukan ; Basta, Ivana  ; Khang, Rin; Lee, Eugene; Stević, Zorica  ; Ralić, Branislav; Tubić, Radoje  ; Seo, GoHun; Marković, Vladana  ;
Božović, Ivo ; Svetel, Marina  ; Marjanović, Ana  ; Veselinović, Nikola; Mesaroš, Šarlota  ; Janković, Milena  ; Savić-Pavićević, Dušanka  ; Jovin, Zita; Novaković, Ivana  ; Lee, Hane; Perić, Stojan  ;
Article
23M23
2023Whole exome sequencing in Serbian patients with hereditary spastic paraplegiaIvanović, Vukan ; Branković, Marija  ; Božović, Ivo ; Stević, Zorica  ; Basta, Ivana  ; Marković, Vladana  ; Svetel, Marina  ; Tubić, Radoje  ; Marjanović, Ana  ; Veselinović, Nikola  ;
Mesaroš, Šarlota  ; Janković, Milena  ; Rakočević-Stojanović, Vidosava ; Savić-Pavićević, Dušanka  ; Novaković, Ivana  ; Perić, Stojan  ;
Conference Paper
Mp. category will be shown later
2022Clinical score for early diagnosis of myotonic dystrophy type 2Ivanović, Vukan ; Perić, Stojan Z.  ; Pešović, Jovan  ; Tubić, Radoje  ; Božović, Ivo  ; Palibrk, Aleksa; Basta, Ivana Z.  ; Savić-Pavićević, Dušanka Lj.  ; Rakočević-Stojanović, Vidosava M. Conference Paper
Mp. category will be shown later
2022Clinical score for early diagnosis of myotonic dystrophy type 2Ivanović, Vukan ; Perić, Stojan  ; Pešović, Jovan  ; Tubić, Radoje  ; Božović, Ivo ; Petrović-Đorđević, Ivana; Savić-Pavićević, Dušanka  ; Meola, Giovanni; Stojanović-Rakočević, Vidosava Article
22M22
2020Yield of the PMP22 deletion analysis in patients with compression neuropathiesIvanović, Vukan ; Branković. Marija  ; Bjelica, Bogdan ; Kačar, Aleksandra  ; Tubić, Radoje  ; Janković, Milena  ; Marjanović, Ana  ; Novaković, Ivana  ; Rakočević-Stojanović, Vidosava ; Perić, Stojan  Article
21M21