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

Refined By:
Date Issued:  [2010 TO 2016]

Results 1-25 of 28 (Search time: 0.013 seconds).

Issue DateTitleAuthor(s)Rank
120-May-2016Application of rapidly/fast mutated Y- STR loci analzsis in Serbia: haplotype and mutation analysis with nine generation family tree reconstructionKecmanović, Miljana ; Čokić, V.; Keckarević-Marković, Milica ; Keckarević, Dušan M34
22-May-2016Genetics of lafora progressive myoclonic epilepsy: Current perspectivesKecmanović, Miljana ; Keckarević Marković, Milica ; Keckarević, Dušan ; Stevanović, Galina; Jović, Nebojša; Romac, Stanka
3May-2016Analysis of PMP22 duplication and deletion using a panel of six dinucleotide tandem repeatsGagic, Milica; Keckarević Marković, Milica ; Kecmanović, Miljana ; Keckarević, Dušan ; Mladenovic, Jelena; Dackovic, Jelena; Milic-Rasic, Vedrana; Romac, Stanka
4Jan-2016Clinical and genetic data on Lafora disease patients of Serbian/Montenegrin originKecmanović, Miljana ; Jović, N.; Keckarević Marković, Milica ; Keckarević, Dušan ; Stevanović, G.; Ignjatović, P.; Romac, S.
52015Is it easy to recognize HINT1 neuropathy (oral presentation)Milić Rašić, V.; Branković, V.; Mladenović, J.; Nikodinović, J.; Kosac, A.; Baets, J.; De Jonghe, P.; Jordanova, A.; Zimon, M.; Keckarević-Marković, Milica ; Savić-Pavićević, Dušanka ; Todorović, S.M34
62015Population analysis of the European standard set (ESS) loci and SE33 locus in a Republic of SerbiaJakovski, Z.; Keckarević, Dušan ; Dogan, S.; Jankova Ajanovska, R.; Keckarević-Marković, Milica ; Marjanović, D.M34
72015Elevated level of creatinine phosphokinase in the blood of patients with peripheral polyneuropathiesMladenović, Ј.; Nikodinovic-Glumac, Ј.; Kosac, A.; Keckarević-Marković, Milica ; Baets, J.; Milić Rasić, V.M34
8Feb-2014A shared haplotype indicates a founder event in unverricht-lundborg disease patients from SerbiaKecmanović, Miljana ; Ristić, Aleksandar J.; Ercegovac, Marko; Keckarević Marković, Milica ; Keckarević, Dušan ; Sokić, Dragoslav; Romac, Stanka
92014PALM-LCM in sexual assault casesŽivković, J.; Ostojić, L.; Kecmanović, Miljana ; Keckarević-Marković, Milica ; Keckarević, Dušan M64
102014Microsatellite analysis in CMT1A genetic testingGagić, M.; Keckarević-Marković, Milica ; Keckarević, Dušan ; Kecmanović, Miljana ; Mladenović, J.; Milić Rašić, V.; Romac, S.M64
112014Deletion of NHLRC1 gene is founder mutation in Lafora disease patients of Serbian/Montenegrim originKecmanović, Miljana ; Jović, N.; Keckarević-Marković, Milica ; Keckarević, Dušan ; Stevanović, G.; Romac, S.M64
122014Analysis of hexanucleotide GGGGCC repeats in the first intron of the C9orf72 geneLabus, O.; Keckarević, Dušan ; Keckarević-Marković, Milica ; Kecmanović, Miljana ; Romac, S.M64
1325-Jun-2013Mutations in PMP22, MPZ0 and GJB1 in Serbian CMT patients: phenotypes and mechanisms of pathogenicityKeckarević-Marković, Milica ; Kecmanović, Miljana ; Keckarević, Dušan ; Dacković, J.; Mladenović, J.; Milić-Rasić, V.; Romac, S.M34
1425-Jun-2013CCFDN in Serbian patients-does uniform genotypes mean uniform phenotype?Nikodinović Glumac, J.; Milić-Rasić, V.; Keckarević-Marković, Milica ; Mladenović, J.M34
1525-Jun-2013Quality of life in patients with Charcot-Marie- Tooth disease in population of BeolgradeMladenović, J.; Milić-Rasić, V.; Keckarević-Marković, Milica ; Romac, S.; Todorović, S.; Rakočević Stojanović, V.; Kisić Tepavčević, D.; Hofman, A.; Pekmezović, T.M34
1625-Jun-2013Clinical and neurophysiologic charactersitics of HINT1 neuropathy in Serbian patientsMilić-Rasić, M.; Nikodinović, J.; Mladenović, J.; Jordanova, A.; Baets, J.; Zimon, M.; De Jonghe, P.; Keckarević-Marković, Milica ; Todorović, S.M34
1715-Feb-2013Lafora disease: Severe phenotype associated with homozygous deletion of the NHLRC1 geneKecmanović, Miljana ; Jović, Nebojša; Čukić, Mirjana; Keckarević Marković, Milica ; Keckarević, Dušan ; Stevanović, Galina; Romac, Stanka
18Jan-2013An algorithm for genetic testing of serbian patients with demyelinating charcot-marie-toothKeckarević Marković, Milica P. ; Dackovic, Jelena; Mladenovic, Jelena; Milic-Rasic, Vedrana; Kecmanović, Miljana ; Keckarević, Dušan ; Romac, Stanka
192013Rabdomioliza 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
208-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
218-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
228-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
239-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
24Feb-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
252012Neurofiziološke 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