WDR45 mutations may cause a MECP2 mutation-negative Rett syndrome phenotype

Por Kulikovskaja, Leonora, Sarajlija, Adrijan, Savic-Pavicevic, Dusanka, Dobricic, Valerija, Klein, Christine, Westenberger, Ana
Publicado no Neurol Genet (2018)

Molecular Genetics and Genetic Testing in Myotonic Dystrophy Type 1

Por Savić Pavićević, Dušanka, Miladinović, Jelena, Brkušanin, Miloš, Šviković, Saša, Djurica, Svetlana, Brajušković, Goran, Romac, Stanka
Publicado em 2013

Endothelial nitric oxide synthase gene polymorphisms and prostate cancer risk in Serbian population

Por Branković, Ana, Brajušković, Goran, Nikolić, Zorana, Vukotić, Vinka, Cerović, Snežana, Savić-Pavićević, Dušanka, Romac, Stanka
Publicado em 2013

Personality traits in patients with myotonic dystrophy type 2

Por Paunic, Teodora, Peric, Stojan, Parojcic, Aleksandra, Savic-Pavicevic, Dusanka, Vujnic, Milorad, Pesovic, Jovan, Basta, Ivana, Lavrnic, Dragana, Rakocevic-Stojanovic, Vidosava
Publicado no Acta Myol (2017)

Multidimensional aspects of pain in myotonic dystrophies

Por Peric, Marina, Peric, Stojan, Rapajic, Nada, Dobricic, Valerija, Savic-Pavicevic, Dusanka, Nesic, Ivana, Radojicic, Svetlana, Novakovic, Ivana, Lavrnic, Dragana, Rakocevic-Stojanovic, Vidosava
Publicado no Acta Myol (2015)

Assessment of Association between Common Variants at 17q12 and Prostate Cancer Risk—Evidence from Serbian Population and Meta‐Analysis

Por Nikolić, Zorana Z., Branković, Ana S., Savić‐Pavićević, Dušanka L.J., Preković, Stefan M., Vukotić, Vinka D., Cerović, Snežana J., Filipović, Nataša N., Tomović, Saša M., Romac, Stanka P., Brajušković, Goran N.
Publicado no Clin Transl Sci (2014)

A novel recessive TTN founder variant is a common cause of distal myopathy in the Serbian population

Por Perić, Stojan, Glumac, Jelena Nikodinović, Töpf, Ana, Savić-Pavićević, Dušanka, Phillips, Lauren, Johnson, Katherine, Cassop-Thompson, Marcus, Xu, Liwen, Bertoli, Marta, Lek, Monkol, MacArthur, Daniel, Brkušanin, Miloš, Milenković, Sanja, Rašić, Vedrana Milić, Banko, Bojan, Maksimović, Ružica, Lochmüller, Hanns, Stojanović, Vidosava Rakočević, Straub, Volker
Publicado no Eur J Hum Genet (2017)