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Full Name
Keckarević-Marković, Milica
 
Email
milica@bio.bg.ac.rs
 
 
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Publications

Results 76-100 of 101 (Search time: 0.016 seconds).

Issue DateTitleAuthor(s)Rank
7631-May-2008Frequency of the hemochromatosis gene mutations in patients with hereditary hemochromatosis and in control subjects from SerbiaŠarić, M.; Zamurović, L.; Keckarević-Marković, Milica ; Keckarević, Dušan ; Kecmanović, Miljana ; Savić-Pavićević, Dušanka ; Jović, J.; Romac, S.M34
7731-May-2008Coexistence of Unvericht-Lundborg disease and congenital deafness in one Serbian familyKecmanović, Miljana ; Ristić, A.; Sokić, D.; Keckarević-Marković, Milica ; Keckarević, Dušan ; Romac, S.M34
7831-May-2008A three generation Serbian family with C263T mutation in MPZ geneKeckarević-Marković, Milica ; Dačković, J.; Mladenović, J.; Kecmanović, Miljana ; Keckarević, Dušan ; Milić-Rašić, V.; Romac, S.M34
79Mar-2008HD phenocopies - Possible role of saitohin geneJanković, N.; Kecmanović, M. ; Dimitrijević, R.; Keckarević Marković, M. ; Dobričić, V.; Keckarević, D. ; Savić Pavićević, D. ; Romac, S.
8013-Sep-2007Human Y-specific STR haplotypes in population of Serbia and MontenegroStevanović, Miljana ; Dobričić, Valerija; Keckarević, Dušan ; Perović, Aleksandar; Savić Pavićević, Dušanka ; Keckarević Marković, Milica ; Jovanović, Aleksandar; Romac, Stanka
811-Aug-2007Survival of Huntington's disease patients in Serbia: Longer survival in female patientsPekmezovic, Tatjana; Svetel, Marina; Maric, Jelena; Dujmovic-Basuroski, Irena; Dragasevic, Natasa; Keckarevic, Milica ; Romac, Stanka; Kostic, Vladimir S.
8216-Jun-2007Unverricht-Lundborg disease: the first report of genetically confirmed case in SerbiaKecmanović, Miljana ; Ercegovac, M.; Dimitrijević, R.; Dobričić, V.; Keckarević-Marković, Milica ; Savić-Pavićević, Dušanka ; Šarić, M.; Keckarević, Dušan ; Beslać-Bumbaširević, Lj.; Romac, S.M34
8316-Jun-2007Hereditary Motor and Sensory Neuropathy type Lom in Serbian Romani familyKeckarević-Marković, Milica ; Milić-Rašić, V.; Dobričić, V.; Kecmanović, Miljana ; Dimitrijević, R.; Šarić, M.; Savić-Pavićević, Dušanka ; Keckarević, Dušan ; Todorović, S.; Romac, S.M34
842007Frequency of the hemochromatosis gene mutations in patients with hereditary hemochromatosis and in control subjects from Serbia and MontenegroŠarić, M.; Zamurović, Lj.; Keckarević-Marković, Milica ; Keckarević, Dušan ; Kecmanović, Miljana ; Savić-Pavićević, Dušanka ; Jović, J.; Romac, S.M34
85Aug-2006Frequency 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
86Feb-2006Frequency analysis and clinical characterization of different types of spinocerebellar ataxia in Serbian patientsDragašević, 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.
875-Sep-2005Friedreich’s ataxia: analysis of mitotic instabilityDobričić, V.; Keckarević-Marković, Milica ; Stevanović, M.; Šarić, M.; Savić, D.; Keckarević, Dušan ; Romac, S.M34
8816-Jul-2005Population 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
89Apr-2005JP-3 gene polymorphism in a healthy population of Serbia and MontenegroKeckarević, M. ; Savić, D. ; Romac, S.
90Feb-2005Yugoslav HD phenocopies analyzed on the presence of mutations in PrP, ferritin and JP-3 genesKeckarević, Milica ; Savić, Dušanka ; Svetel, Marina; Kostić, Vladimir; Vukosavić, Slobodanka; Romac, Stanka
912005Analiza genskih mutacija kod pacijenata sa naslednim neuropatijamaMilić Rašić, V.; Todorović, S.; Keckarević-Marković, Milica ; Romac, S.M45
922005Molekularna genetika distrofinopatijaKeckarević-Marković, Milica ; Romac, S.M45
932005Linkage analysis by microsatellite repeats on a Duchenne muscular dystrophy family: a case reportKeckarević-Marković, Milica ; Dobričić, V.; Stevanović, M. ; Šarić, M.; Savić, D.; Keckarević, Dušan ; Romac, S.M34
942004Molekularna biologija i genotipsko-fenotipske korelacije Fridrajhove ataksijeKeckarević-Marković, Milica ; Branković-Srećković, V.M45
952004' Mogućnosti molekularne dijagnostike hereditarne hemohromatoze tip1 u Srbiji i Crnoj GoriZamurović, Lj.; Šarić, M.; Keckarević-Marković, Milica ; Čuljković, B.; Jović, J.; Romac, S.M64
9619-Jun-2003Survival of Huntington patients in SerbiaDragašević, N.; Pekmezović, T.; Svetel, M.; Marić, J.; Dujmović, I.; Keckarević-Marković, Milica ; Kostić, V.M34
972003Molekularna genetika migrene razvojnog dobaJančić-Stefanović, J.; Keckarević-Marković, Milica M45
982003Molekularna genetika distrofinopatijaKeckarević-Marković, Milica M45
99Oct-2002Genetic and clinical analysis of spinocerebellar ataxia type 8 repeat expansion in YugoslaviaTopisirovic, I.; Dragaševic, N.; Savic, D. ; Ristic, A.; Keckarevic, M. ; Keckarevic, D. ; Culjkovic, B.; Petrovic, I.; Romac, S.; Kostic, V. S.
100May-2002Duchenne'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