Kecmanović, Miljana
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Full Name
Kecmanović, Miljana
Main Affiliation
Email
miljana@bio.bg.ac.rs
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Results 26-46 of 46 (Search time: 0.011 seconds).
| Issue Date | Title | Author(s) | Rank | |
|---|---|---|---|---|
| 26 | 2017 | Updates to the Lafora Epilepsy Cure Initiative (LECI) Clinical Center: Development of a data collection tool for measurement of Lafora Epilepsy Disease Progression | Nguyen, V-H.; Serratosa, JM.; Gonzales, B.; Genton, P.; Michelucci, R.; Sinha, S.; Chandra, S.; Beydoun, A.; Arabi, M.; Kecmanović, Miljana ; Whitehouse, W.; Martinez-Juarez, IM.; Guilhoto, L.; Salas-Puig, J.; Ben- Menachem, E.; Goldsmith, D.; Duron, RM.; Medina, MT.; Bailey, JN.; Gentry, M.; Minassian, B.; Delgado- Escueta, AV. | M34 |
| 27 | 2017 | Clinical Center for the Lafora Epilepsy Cure Initiative (LECI): Clinical trial readiness for a global curative drug trial (P2.245) | Nguyen, V-H.; Duron, RM.; Serratosa, JM.; Minassian, B.; Michelucci, R.; Genton, P.; Sinha, S.; Arabi, M.; Beydoun, A.; Ben-Menachem, E.; Kecmanović, Miljana ; Guilhoto, L.; Whitehouse, W.; Salas-Puig, J.; Martinez- Juarez, I.; Gentry, M.; Bailey, J.; Delgado-Escueta, AV. | M34 |
| 28 | 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 |
| 29 | 2014 | Microsatellite analysis in CMT1A genetic testing | Gagić, M.; Keckarević-Marković, Milica ; Keckarević, Dušan ; Kecmanović, Miljana ; Mladenović, J.; Milić Rašić, V.; Romac, S. | M64 |
| 30 | 2014 | PALM-LCM in sexual assault cases | Živković, J.; Ostojić, L.; Kecmanović, Miljana ; Keckarević-Marković, Milica ; Keckarević, Dušan | M64 |
| 31 | 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 |
| 32 | 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 |
| 33 | 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 |
| 34 | 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 |
| 35 | 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 |
| 36 | 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 |
| 37 | 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 |
| 38 | 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 |
| 39 | 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 |
| 40 | 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 |
| 41 | 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 |
| 42 | 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 |
| 43 | 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 |
| 44 | 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 |
| 45 | 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 |
| 46 | 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 |