Browsing by Author Rakočević-Stojanović, Vidosava

Showing results 1 to 4 of 4
Issue DateTitleAuthor(s)Rank
18-Jul-2022Autoimmune Diseases in Patients With Myotonic Dystrophy Type 2Perić, Stojan; Zlatar, Jelena; Nikolić, Luka; Ivanović, Vukan; Pešović, Jovan ; Petrovic Đorđevic, Ivana; Srećković, Svetlana; Savić-Pavićević, Dušanka ; Meola, Giovanni; Rakočević-Stojanović, VidosavaM22
30-Jun-2022Cognitive assessment in patients with myotonic dystrophy type 2Perić, Stojan; Gunjić, Ilija; Delić, Neda; Stojiljkovic Tamas, Olivera; Salak-Đokic, Biljana; Pešović, Jovan ; Petrović Đorđevic, Ivana; Ivanović, Vukan; Savić-Pavićević, Dušanka ; Meola Giovanni; Rakočević-Stojanović, VidosavaM22
1-Dec-2001Is the 31 CAG repeat allele of the spinocerebellar ataxia 1 (SCA1) gene locus non-specifically associated with trinucleotide expansion diseases?Savić, Dušanka ; Topisirović, Ivan; Keckarević, Milica ; Keckarević, Dušan ; Major, Tamara; Čuljković, Biljana; Stojković, Oliver; Rakočević-Stojanović, Vidosava; Mladenović, Jelena; Todorović, Slobodanka; Apostolski, Slobodan; Romac, Stanka
27-Nov-2018Repeat Interruptions Modify Age at Onset in Myotonic Dystrophy Type 1 by Stabilizing DMPK Expansions in Somatic CellsPešović, Jovan ; Perić, Stojan; Brkušanin, Miloš ; Brajušković, Goran ; Rakočević-Stojanović, Vidosava; Savić Pavićević, Dušanka