Browsing by Author Romac, Stanka
Showing results 6 to 25 of 32
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Issue Date | Title | Author(s) | Rank |
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2005 | Bcl-2 and Bax protein interaction in B-lymphocytes of peripheral blood in patients with chronic lymphocytic leukemia | Brajušković, Goran ; Vukosavić Orolički, Slobodanka; Cerović, Snežana; Knežević Ušaj, Slavica; Marjanović, Slobodan; Romac, Stanka | M52 |
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 | |
May-2002 | Duchenne's and Becker's muscular dystrophy: analysis of phenotype-genotype correlation in 28 patients] | Keckarević, Milica ; Savić, Dušanka ; Culjković, Biljana; Zamurović, Natasa; Major, Tamara; Keckarević, Dušan ; Todorović, Slobodanka; Romac, Stanka | |
Dec-2013 | Endothelial nitric oxide synthase gene polymorphisms and prostate cancer risk in serbian population | Branković, Ana; Brajušković, Goran ; Nikolić, Zorana; Vukotić, Vinka; Cerović, Snežana; Savić Pavićević, Dušanka ; Romac, Stanka | |
2004 | Expression of the Bcl-2 family of proteins in peripheral blood B-lymphocytes in patients with chronic lymphocytic leukemia | Brajušković, Goran ; Vukosavić Orolički, Slobodanka; Dimitrijević, Jovan; Cerović, Snežana; Knežević Ušaj, Slavica; Marjanović, Slobodan; Romac, Stanka; Škaro Milić, Anđelija | M52 |
Feb-2006 | Frequency analysis and clinical characterization of different types of spinocerebellar ataxia in Serbian patients | Dragašević, Nataša T.; Čuljković, Biljana; Klein, Christine; Ristić, Aleksandar; Keckarević, Milica ; Topisirović, Ivan; Vukosavić, Slobodanka; Svetel, Marina; Kock, Norman; Stefanova, Elka; Romac, Stanka; Kostić, Vladimir S. | |
Aug-2006 | Frequency of the hemochromatosis gene mutations in the population of Serbia and Montenegro [2] | Šarić, M.; Zamurović, Lj; Keckarević Marković, M. ; Keckarević, D. ; Stevanović, M. ; Savić Pavićević, D. ; Jović, J.; Romac, Stanka | |
2-May-2016 | Genetics of lafora progressive myoclonic epilepsy: Current perspectives | Kecmanović, Miljana ; Keckarević Marković, Milica ; Keckarević, Dušan ; Stevanović, Galina; Jović, Nebojša; Romac, Stanka | |
13-Sep-2007 | Human Y-specific STR haplotypes in population of Serbia and Montenegro | Stevanović, Miljana ; Dobričić, Valerija; Keckarević, Dušan ; Perović, Aleksandar; Savić Pavićević, Dušanka ; Keckarević Marković, Milica ; Jovanović, Aleksandar; Romac, Stanka | |
1-Dec-2001 | Is 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 | |
1-Jun-2015 | Joint effect of ADARB1 gene, HTR2C gene and stressful life events on suicide attempt risk in patients with major psychiatric disorders | Karanović, Jelena ; Šviković, Saša; Pantović, Maja; Durica, Svetlana; Brajušković, Goran ; Damjanović, Aleksandar; Jovanović, Vladimir; Ivković, Maja; Romac, Stanka; Savić Pavićević, Dušanka | |
1-Nov-2015 | Joint effect of the SMN2 and SERF1A genes on childhood-onset types of spinal muscular atrophy in Serbian patients | Brkušanin, Miloš ; Kosać, Ana; Jovanović, Vladimir; Pešović, Jovan ; Brajušković, Goran ; Dimitrijević, Nikola; Todorović, Slobodanka; Romac, Stanka; Milić Rašić, Vedrana; Savić Pavićević, Dušanka | |
15-Feb-2013 | Lafora disease: Severe phenotype associated with homozygous deletion of the NHLRC1 gene | Kecmanović, Miljana ; Jović, Nebojša; Čukić, Mirjana; Keckarević Marković, Milica ; Keckarević, Dušan ; Stevanović, Galina; Romac, Stanka | |
29-Apr-2013 | Molecular genetics and genetic testing in myotonic dystrophy type 1 | Savić Pavićević, Dušanka ; Karanović, Jelena ; Brkušanin, Miloš ; Šviković, Saša; Djurica, Svetlana; Brajušković, Goran ; Romac, Stanka | M23 |
Sep-2011 | Molecular genetics of diseases with unstable expansion of repeats | Savić-Pavićević, Dušanka ; Mladenović, Jelena; Rakočević Stojanović, Vidosava; Pekmezović, T; Karanović, Jelena ; Brajušković, Goran ; Apostolski, Slobodan; Todorović, Slobodanka; Romac, Stanka | M62 |
Jun-2009 | Mutational analysis of GJB1, MPZ, PMP22, EGR2, and LITAF/SIMPLE in Serbian Charcot-Marie-Tooth patients | Keckarević Marković, Milica ; Milic-Rasic, Vedrana; Mladenovic, Jelena; Dackovic, Jelena; Kecmanović, Miljana ; Keckarević, Dušan ; Savić Pavićević, Dušanka ; Romac, Stanka | |
Feb-2012 | A novel P66S mutation in exon 3 of the SOD1 gene with early onset and rapid progression | Keckarević, Dušan ; Stević, Zorica; Keckarević Marković, Milica ; Kecmanović, Miljana ; Romac, Stanka | |
Jul-2010 | Polymorphisms of the prion protein gene (PRNP) in a Serbian population | Dimitrijević, Rajna; Čadež, Ivana; Keckarević Marković, Milica ; Keckarević, Dušan ; Kecmanović, Miljana ; Dobričić, Valerija; Savić Pavićević, Dušanka ; Brajušković, Goran ; Romac, Stanka | |
16-Jul-2005 | Population data on 14 STR loci from population of Serbia and Montenegro (new and renewed data) | Keckarević, Dušan ; Savić, Dušanka ; Keckarević, Milica ; Stevanović, Miljana ; Tarasjev, Aleksej; Čuljković, Biljana; Darmati, Ana; Vukosavić, Slobodanka; Romac, Stanka | |
2011 | Programmed cell death proteins and chronic leukemia | Brajušković, Goran ; Strnad, Milica; Cerović, Snežana; Romac, Stanka |