Loading... 1 0 20 0 false
Full Name
Keckarević-Marković, Milica
 
Email
milica@bio.bg.ac.rs
 
 
Loading... 2 0 20 0 false

Publications

Results 76-100 of 118 (Search time: 0.014 seconds).

Issue DateTitleAuthor(s)Rank
762013Rabdomioliza kao dijagnostički i terapijski izazov kod hereditarne neuropatije sa kongenitalnom kataraktom i facijalnim dismorfizmomNikodinović Glumac, J.; Milić Rašić, V.; Keckarević-Marković, Milica ; Milenković, S.M64
778-Sep-2012Over- representation of the L144F SOD1mutation in Serbian ALS patients due tofounder effectKeckarević, Dušan ; Stević, Z.; Keckarević-Marković, Milica ; Kecmanović, Miljana ; Romac, S.M34
788-Sep-2012Founder c.1048-1049delGA mutation in NHLRC1 gene in Lafora’s disease patients from SerbiaKecmanović, Miljana ; Jović, N.; Keckarević-Marković, Milica ; Keckarević, Dušan ; Stevanović, G.; Romac, S.M34
798-Sep-2012Founder R32G mutation in GJB1 gene of Serbian CMT patientsKeckarević-Marković, Milica ; Kecmanović, Miljana ; Keckarević, Dušan ; Mladenović, J.; Milić-Rasić, V.; Romac, S.M34
809-Jul-2012The advancement of molecular diagnostics of CMT in SerbiaKeckarević-Marković, Milica ; Milić-Rašić, V.; Mladenović, J.; Dačković, J.; Kecmanović, Miljana ; Keckarević, Dušan ; Romac, S.M34
81Feb-2012A novel P66S mutation in exon 3 of the SOD1 gene with early onset and rapid progressionKeckarević, Dušan ; Stević, Zorica; Keckarević Marković, Milica ; Kecmanović, Miljana ; Romac, Stanka
822012Neurofiziološke i kliničke karakteristike neuromiotonije u novoj neuromišićnoj bolestiMilić-Rašić, M.; Nikodinović, J.; De Jonghe, P.; Jordanova, A.; Baets, J.; Zimon, M.; Keckarević-Marković, Milica ; Savić-Pavićević, Dušanka ; Todorović, S.M64
831-Jun-2011Epidemiology of Charcot-Marie-Tooth disease in the population of Belgrade, SerbiaMladenovic, J.; Milic Rasic, V.; Keckarević Marković, M. ; Romac, S.; Todorovic, S.; Rakocevic Stojanovic, V.; Kisic Tepavcevic, D.; Hofman, A.; Pekmezovic, T.
84Jul-2010Schizophrenia and apolipoprotein e gene polymorphism in Serbian populationKecmanović, Miljana ; Dobričić, Valerija; Dimitrijević, Rajna; Keckarević, Dušan ; Savić Pavićević, Dušanka ; Keckarević Marković, Milica ; Ivkovic, Maja; Romac, Stanka
85Jul-2010Polymorphisms of the prion protein gene (PRNP) in a Serbian populationDimitrijević, Rajna; Čadež, Ivana; Keckarević Marković, Milica ; Keckarević, Dušan ; Kecmanović, Miljana ; Dobričić, Valerija; Savić Pavićević, Dušanka ; Brajušković, Goran ; Romac, Stanka
8620-Jun-2009Congenital cataracts facial dysmorphism neuropathy in Serbian Romani patientsKeckarević-Marković, Milica ; Milić-Rašić, V.; Kecmanović, Miljana ; Keckarević, Dušan ; Romac, S.M34
87Jun-2009Coexistence of Unverricht-Lundborg disease and congenital deafness: Molecular resolution of a complex comorbidityKecmanović, Miljana ; Ristić, Aleksandar J.; Sokić, Dragoslav; Keckarević Marković, Milica ; Vojvodić, Nikola; Ercegovac, Marko; Janković, Slavko; Keckarević, Dušan ; Savić Pavićević, Dušanka ; Romac, Stanka
88Jun-2009Mutational analysis of GJB1, MPZ, PMP22, EGR2, and LITAF/SIMPLE in Serbian Charcot-Marie-Tooth patientsKeckarević Marković, Milica ; Milic-Rasic, Vedrana; Mladenovic, Jelena; Dackovic, Jelena; Kecmanović, Miljana ; Keckarević, Dušan ; Savić Pavićević, Dušanka ; Romac, Stanka
892009&Molekularna analiza Gli3 gena kod pacijenata sa Palister-Halovim sindromomRadivojević, M.; Keckarević-Marković, Milica ; Dačković, J.; Apostolski, S.; Brajušković, Goran ; Romac, S.M64
90Oct-2008Hereditary motor and sensory neuropathy Lom type in a Serbian familyDačković, Jalena; Keckarević-Marković, M. ; Komazec, Z.; Rakočević-Stojanović, V.; Lavrnić, D.; Stević, Z.; Ribarić, K.; Romac, S.; Apostolski, S.
917-Jun-2008Mutations in NHLRC1 gene are predominant cause of Lafora disease in Serbian populationKecmanović, Miljana ; Jović, N.; Keckarević-Marković, Milica ; Dobričić, V.; Keckarević, Dušan ; Ignjatović, P.; Romac, S.M34
927-Jun-2008A novel 9-bp duplication in the connexin 32 gene causing X-linked Charcot-Marie-Tooth diseaseKeckarević-Marković, Milica ; Milić-Rašić, V.; Kecmanović, Miljana ; Keckarević, D.; Todorović, S.; Romac, S.M34
9331-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
9431-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
9531-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
96Mar-2008HD phenocopies - Possible role of saitohin geneJanković, N.; Kecmanović, M. ; Dimitrijević, R.; Keckarević Marković, M. ; Dobričić, V.; Keckarević, D. ; Savić Pavićević, D. ; Romac, S.
9713-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
981-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.
9916-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
10016-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