Browsing by Author Ercegovac, Marko
Showing results 1 to 3 of 3
| Issue Date | Title | Author(s) | Rank |
|---|---|---|---|
| Jun-2009 | Coexistence of Unverricht-Lundborg disease and congenital deafness: Molecular resolution of a complex comorbidity | Kecmanović, Miljana ; Ristić, Aleksandar J.; Sokić, Dragoslav; Keckarević Marković, Milica ; Vojvodić, Nikola; Ercegovac, Marko; Janković, Slavko; Keckarević, Dušan ; Savić Pavićević, Dušanka ; Romac, Stanka | |
| Nov-2015 | GSTA1, GSTM1, GSTP1 and GSTT1 polymorphisms in progressive myoclonus epilepsy: A Serbian case-control study | Ercegovac, Marko; Jovic, Nebojsa; Sokic, Dragoslav; Savic-Radojevic, Ana; Coric, Vesna; Radic, Tanja; Nikolic, Dimitrije; Kecmanović, Miljana ; Matic, Marija; Simic, Tatjana; Pljesa-Ercegovac, Marija | |
| Feb-2014 | A shared haplotype indicates a founder event in unverricht-lundborg disease patients from Serbia | Kecmanović, Miljana ; Ristić, Aleksandar J.; Ercegovac, Marko; Keckarević Marković, Milica ; Keckarević, Dušan ; Sokić, Dragoslav; Romac, Stanka |