Keckarević-Marković, Milica
Loading...
1
0
20
0
false
Full Name
Keckarević-Marković, Milica
Main Affiliation
Email
milica@bio.bg.ac.rs
Loading...
2
0
20
0
false
Results 51-74 of 74 (Search time: 0.005 seconds).
| Issue Date | Title | Author(s) | Rank | |
|---|---|---|---|---|
| 51 | 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 |
| 52 | 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 |
| 53 | 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 |
| 54 | 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 |
| 55 | 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 |
| 56 | 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 |
| 57 | 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 |
| 58 | 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 |
| 59 | 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 |
| 60 | 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 |
| 61 | 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 |
| 62 | 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 |
| 63 | 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 |
| 64 | 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 |
| 65 | 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 |
| 66 | 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 |
| 67 | 31-May-2008 | A three generation Serbian family with C263T mutation in MPZ gene | Keckarević-Marković, Milica ; Dačković, J.; Mladenović, J.; Kecmanović, Miljana ; Keckarević, Dušan ; Milić-Rašić, V.; Romac, S. | M34 |
| 68 | 16-Jun-2007 | Hereditary Motor and Sensory Neuropathy type Lom in Serbian Romani family | Keckarević-Marković, Milica ; Milić-Rašić, V.; Dobričić, V.; Kecmanović, Miljana ; Dimitrijević, R.; Šarić, M.; Savić-Pavićević, Dušanka ; Keckarević, Dušan ; Todorović, S.; Romac, S. | M34 |
| 69 | 16-Jun-2007 | Unverricht-Lundborg disease: the first report of genetically confirmed case in Serbia | Kecmanović, Miljana ; Ercegovac, M.; Dimitrijević, R.; Dobričić, V.; Keckarević-Marković, Milica ; Savić-Pavićević, Dušanka ; Šarić, M.; Keckarević, Dušan ; Beslać-Bumbaširević, Lj.; Romac, S. | M34 |
| 70 | 2007 | Frequency of the hemochromatosis gene mutations in patients with hereditary hemochromatosis and in control subjects from Serbia and Montenegro | Šarić, M.; Zamurović, Lj.; Keckarević-Marković, Milica ; Keckarević, Dušan ; Kecmanović, Miljana ; Savić-Pavićević, Dušanka ; Jović, J.; Romac, S. | M34 |
| 71 | 5-Sep-2005 | Friedreich’s ataxia: analysis of mitotic instability | Dobričić, V.; Keckarević-Marković, Milica ; Stevanović, M.; Šarić, M.; Savić, D.; Keckarević, Dušan ; Romac, S. | M34 |
| 72 | 2005 | Linkage analysis by microsatellite repeats on a Duchenne muscular dystrophy family: a case report | Keckarević-Marković, Milica ; Dobričić, V.; Stevanović, M. ; Šarić, M.; Savić, D.; Keckarević, Dušan ; Romac, S. | M34 |
| 73 | 2004 | ' Mogućnosti molekularne dijagnostike hereditarne hemohromatoze tip1 u Srbiji i Crnoj Gori | Zamurović, Lj.; Šarić, M.; Keckarević-Marković, Milica ; Čuljković, B.; Jović, J.; Romac, S. | M64 |
| 74 | 19-Jun-2003 | Survival of Huntington patients in Serbia | Dragašević, N.; Pekmezović, T.; Svetel, M.; Marić, J.; Dujmović, I.; Keckarević-Marković, Milica ; Kostić, V. | M34 |