Keckarević-Marković, Milica
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Full Name
Keckarević-Marković, Milica
Main Affiliation
Email
milica@bio.bg.ac.rs
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Results 1-18 of 18 (Search time: 0.008 seconds).
| Issue Date | Title | Author(s) | Rank | |
|---|---|---|---|---|
| 1 | 2-May-2016 | Genetics of lafora progressive myoclonic epilepsy: Current perspectives | Kecmanović, Miljana ; Keckarević Marković, Milica ; Keckarević, Dušan ; Stevanović, Galina; Jović, Nebojša; Romac, Stanka | |
| 2 | May-2016 | Analysis of PMP22 duplication and deletion using a panel of six dinucleotide tandem repeats | Gagic, Milica; Keckarević Marković, Milica ; Kecmanović, Miljana ; Keckarević, Dušan ; Mladenovic, Jelena; Dackovic, Jelena; Milic-Rasic, Vedrana; Romac, Stanka | |
| 3 | 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 | |
| 4 | 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 | |
| 5 | Jan-2013 | An algorithm for genetic testing of serbian patients with demyelinating charcot-marie-tooth | Keckarević Marković, Milica P. ; Dackovic, Jelena; Mladenovic, Jelena; Milic-Rasic, Vedrana; Kecmanović, Miljana ; Keckarević, Dušan ; Romac, Stanka | |
| 6 | 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 | |
| 7 | 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 | |
| 8 | Jul-2010 | Schizophrenia and apolipoprotein e gene polymorphism in Serbian population | Kecmanović, Miljana ; Dobričić, Valerija; Dimitrijević, Rajna; Keckarević, Dušan ; Savić Pavićević, Dušanka ; Keckarević Marković, Milica ; Ivkovic, Maja; Romac, Stanka | |
| 9 | 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 | |
| 10 | 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 | |
| 11 | 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 | |
| 12 | 1-Aug-2007 | Survival of Huntington's disease patients in Serbia: Longer survival in female patients | Pekmezovic, Tatjana; Svetel, Marina; Maric, Jelena; Dujmovic-Basuroski, Irena; Dragasevic, Natasa; Keckarevic, Milica ; Romac, Stanka; Kostic, Vladimir S. | |
| 13 | 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 | |
| 14 | 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. | |
| 15 | 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 | |
| 16 | Feb-2005 | Yugoslav HD phenocopies analyzed on the presence of mutations in PrP, ferritin and JP-3 genes | Keckarević, Milica ; Savić, Dušanka ; Svetel, Marina; Kostić, Vladimir; Vukosavić, Slobodanka; Romac, Stanka | |
| 17 | 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 | |
| 18 | 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 |