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 51-75 of 101 (Search time: 0.017 seconds).
| Issue Date | Title | Author(s) | Rank | |
|---|---|---|---|---|
| 51 | 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 |
| 52 | 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 |
| 53 | 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 |
| 54 | 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 |
| 55 | 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 |
| 56 | 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 |
| 57 | 15-Feb-2013 | Lafora disease: Severe phenotype associated with homozygous deletion of the NHLRC1 gene | Kecmanović, Miljana ; Jović, Nebojša; Čukić, Mirjana; Keckarević Marković, Milica ; Keckarević, Dušan ; Stevanović, Galina; Romac, Stanka | |
| 58 | Jan-2013 | An algorithm for genetic testing of serbian patients with demyelinating charcot-marie-tooth | Keckarević Marković, Milica P. ; Dackovic, Jelena; Mladenovic, Jelena; Milic-Rasic, Vedrana; Kecmanović, Miljana ; Keckarević, Dušan ; Romac, Stanka | |
| 59 | 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 |
| 60 | 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 |
| 61 | 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 |
| 62 | 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 |
| 63 | 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 |
| 64 | Feb-2012 | A novel P66S mutation in exon 3 of the SOD1 gene with early onset and rapid progression | Keckarević, Dušan ; Stević, Zorica; Keckarević Marković, Milica ; Kecmanović, Miljana ; Romac, Stanka | |
| 65 | 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 |
| 16 | 1-Jun-2011 | Epidemiology of Charcot-Marie-Tooth disease in the population of Belgrade, Serbia | Mladenovic, J.; Milic Rasic, V.; Keckarević Marković, M. ; Romac, S.; Todorovic, S.; Rakocevic Stojanovic, V.; Kisic Tepavcevic, D.; Hofman, A.; Pekmezovic, T. | |
| 17 | Jul-2010 | Schizophrenia and apolipoprotein e gene polymorphism in Serbian population | Kecmanović, Miljana ; Dobričić, Valerija; Dimitrijević, Rajna; Keckarević, Dušan ; Savić Pavićević, Dušanka ; Keckarević Marković, Milica ; Ivkovic, Maja; Romac, Stanka | |
| 18 | Jul-2010 | Polymorphisms of the prion protein gene (PRNP) in a Serbian population | Dimitrijević, Rajna; Čadež, Ivana; Keckarević Marković, Milica ; Keckarević, Dušan ; Kecmanović, Miljana ; Dobričić, Valerija; Savić Pavićević, Dušanka ; Brajušković, Goran ; Romac, Stanka | |
| 19 | 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 |
| 20 | Jun-2009 | Mutational analysis of GJB1, MPZ, PMP22, EGR2, and LITAF/SIMPLE in Serbian Charcot-Marie-Tooth patients | Keckarević Marković, Milica ; Milic-Rasic, Vedrana; Mladenovic, Jelena; Dackovic, Jelena; Kecmanović, Miljana ; Keckarević, Dušan ; Savić Pavićević, Dušanka ; Romac, Stanka | |
| 21 | Jun-2009 | Coexistence of Unverricht-Lundborg disease and congenital deafness: Molecular resolution of a complex comorbidity | Kecmanović, Miljana ; Ristić, Aleksandar J.; Sokić, Dragoslav; Keckarević Marković, Milica ; Vojvodić, Nikola; Ercegovac, Marko; Janković, Slavko; Keckarević, Dušan ; Savić Pavićević, Dušanka ; Romac, Stanka | |
| 22 | 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 |
| 23 | Oct-2008 | Hereditary motor and sensory neuropathy Lom type in a Serbian family | Dačković, Jalena; Keckarević-Marković, M. ; Komazec, Z.; Rakočević-Stojanović, V.; Lavrnić, D.; Stević, Z.; Ribarić, K.; Romac, S.; Apostolski, S. | |
| 24 | 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 |
| 25 | 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 |