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 51-75 of 83 (Search time: 0.012 seconds).
| Issue Date | Title | Author(s) | Rank | |
|---|---|---|---|---|
| 51 | 20-May-2016 | Application of rapidly/fast mutated Y- STR loci analzsis in Serbia: haplotype and mutation analysis with nine generation family tree reconstruction | Kecmanović, Miljana ; Čokić, V.; Keckarević-Marković, Milica ; Keckarević, Dušan | M34 |
| 52 | 2015 | Is 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 |
| 53 | 2015 | Elevated level of creatinine phosphokinase in the blood of patients with peripheral polyneuropathies | Mladenović, Ј.; Nikodinovic-Glumac, Ј.; Kosac, A.; Keckarević-Marković, Milica ; Baets, J.; Milić Rasić, V. | M34 |
| 54 | 2015 | Population analysis of the European standard set (ESS) loci and SE33 locus in a Republic of Serbia | Jakovski, Z.; Keckarević, Dušan ; Dogan, S.; Jankova Ajanovska, R.; Keckarević-Marković, Milica ; Marjanović, D. | M34 |
| 55 | 2014 | Microsatellite analysis in CMT1A genetic testing | Gagić, M.; Keckarević-Marković, Milica ; Keckarević, Dušan ; Kecmanović, Miljana ; Mladenović, J.; Milić Rašić, V.; Romac, S. | M64 |
| 56 | 2014 | PALM-LCM in sexual assault cases | Živković, J.; Ostojić, L.; Kecmanović, Miljana ; Keckarević-Marković, Milica ; Keckarević, Dušan | M64 |
| 57 | 2014 | Deletion of NHLRC1 gene is founder mutation in Lafora disease patients of Serbian/Montenegrim origin | Kecmanović, Miljana ; Jović, N.; Keckarević-Marković, Milica ; Keckarević, Dušan ; Stevanović, G.; Romac, S. | M64 |
| 58 | 2014 | Analysis of hexanucleotide GGGGCC repeats in the first intron of the C9orf72 gene | Labus, O.; Keckarević, Dušan ; Keckarević-Marković, Milica ; Kecmanović, Miljana ; Romac, S. | M64 |
| 59 | 25-Jun-2013 | Mutations in PMP22, MPZ0 and GJB1 in Serbian CMT patients: phenotypes and mechanisms of pathogenicity | Keckarević-Marković, Milica ; Kecmanović, Miljana ; Keckarević, Dušan ; Dacković, J.; Mladenović, J.; Milić-Rasić, V.; Romac, S. | M34 |
| 60 | 25-Jun-2013 | Quality of life in patients with Charcot-Marie- Tooth disease in population of Beolgrade | Mladenović, J.; Milić-Rasić, V.; Keckarević-Marković, Milica ; Romac, S.; Todorović, S.; Rakočević Stojanović, V.; Kisić Tepavčević, D.; Hofman, A.; Pekmezović, T. | M34 |
| 61 | 25-Jun-2013 | CCFDN in Serbian patients-does uniform genotypes mean uniform phenotype? | Nikodinović Glumac, J.; Milić-Rasić, V.; Keckarević-Marković, Milica ; Mladenović, J. | M34 |
| 62 | 25-Jun-2013 | Clinical and neurophysiologic charactersitics of HINT1 neuropathy in Serbian patients | Milić-Rasić, M.; Nikodinović, J.; Mladenović, J.; Jordanova, A.; Baets, J.; Zimon, M.; De Jonghe, P.; Keckarević-Marković, Milica ; Todorović, S. | M34 |
| 63 | 2013 | Rabdomioliza kao dijagnostički i terapijski izazov kod hereditarne neuropatije sa kongenitalnom kataraktom i facijalnim dismorfizmom | Nikodinović Glumac, J.; Milić Rašić, V.; Keckarević-Marković, Milica ; Milenković, S. | M64 |
| 64 | 8-Sep-2012 | Over- representation of the L144F SOD1mutation in Serbian ALS patients due tofounder effect | Keckarević, Dušan ; Stević, Z.; Keckarević-Marković, Milica ; Kecmanović, Miljana ; Romac, S. | M34 |
| 65 | 8-Sep-2012 | Founder c.1048-1049delGA mutation in NHLRC1 gene in Lafora’s disease patients from Serbia | Kecmanović, Miljana ; Jović, N.; Keckarević-Marković, Milica ; Keckarević, Dušan ; Stevanović, G.; Romac, S. | M34 |
| 66 | 8-Sep-2012 | Founder R32G mutation in GJB1 gene of Serbian CMT patients | Keckarević-Marković, Milica ; Kecmanović, Miljana ; Keckarević, Dušan ; Mladenović, J.; Milić-Rasić, V.; Romac, S. | M34 |
| 67 | 9-Jul-2012 | The advancement of molecular diagnostics of CMT in Serbia | Keckarević-Marković, Milica ; Milić-Rašić, V.; Mladenović, J.; Dačković, J.; Kecmanović, Miljana ; Keckarević, Dušan ; Romac, S. | M34 |
| 68 | 2012 | Neurofiziološke i kliničke karakteristike neuromiotonije u novoj neuromišićnoj bolesti | Milić-Rašić, M.; Nikodinović, J.; De Jonghe, P.; Jordanova, A.; Baets, J.; Zimon, M.; Keckarević-Marković, Milica ; Savić-Pavićević, Dušanka ; Todorović, S. | M64 |
| 69 | 29-Sep-2011 | Pallister Hall sindrom: porodica iz Srbije | Dačković, J.; Radivojević, M.; Keckarević-Marković, Milica ; Brajušković, Goran ; Romac, S. | M64 |
| 70 | 20-Jun-2009 | Congenital cataracts facial dysmorphism neuropathy in Serbian Romani patients | Keckarević-Marković, Milica ; Milić-Rašić, V.; Kecmanović, Miljana ; Keckarević, Dušan ; Romac, S. | M34 |
| 71 | 2009 | &Molekularna analiza Gli3 gena kod pacijenata sa Palister-Halovim sindromom | Radivojević, M.; Keckarević-Marković, Milica ; Dačković, J.; Apostolski, S.; Brajušković, Goran ; Romac, S. | M64 |
| 72 | 7-Jun-2008 | A novel 9-bp duplication in the connexin 32 gene causing X-linked Charcot-Marie-Tooth disease | Keckarević-Marković, Milica ; Milić-Rašić, V.; Kecmanović, Miljana ; Keckarević, D.; Todorović, S.; Romac, S. | M34 |
| 73 | 7-Jun-2008 | Mutations in NHLRC1 gene are predominant cause of Lafora disease in Serbian population | Kecmanović, Miljana ; Jović, N.; Keckarević-Marković, Milica ; Dobričić, V.; Keckarević, Dušan ; Ignjatović, P.; Romac, S. | M34 |
| 74 | 31-May-2008 | Coexistence of Unvericht-Lundborg disease and congenital deafness in one Serbian family | Kecmanović, Miljana ; Ristić, A.; Sokić, D.; Keckarević-Marković, Milica ; Keckarević, Dušan ; Romac, S. | M34 |
| 75 | 31-May-2008 | Frequency of the hemochromatosis gene mutations in patients with hereditary hemochromatosis and in control subjects from Serbia | Šarić, M.; Zamurović, L.; Keckarević-Marković, Milica ; Keckarević, Dušan ; Kecmanović, Miljana ; Savić-Pavićević, Dušanka ; Jović, J.; Romac, S. | M34 |