Browsing by Author Dobričić, V.
Showing results 1 to 8 of 8
| Issue Date | Title | Author(s) | Rank |
|---|---|---|---|
| 1-Feb-2016 | Comparison of temporal and stride characteristics in myotonic dystrophies type 1 and 2 during dual-task walking | Radovanović, S.; Perić, S.; Savić Pavićević, Dušanka ; Dobričić, V.; Pešović, Jovan ; Kostić, V.; Rakočević-Stojanović, V. | |
| 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 |
| Mar-2008 | HD phenocopies - Possible role of saitohin gene | Janković, N.; Kecmanović, M. ; Dimitrijević, R.; Keckarević Marković, M. ; Dobričić, V.; Keckarević, D. ; Savić Pavićević, D. ; Romac, S. | |
| 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 |
| 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 |
| Dec-2007 | MECP2 mutations in Serbian Rett syndrome patients | Djarmati, A.; Dobričić, V.; Kecmanović, M. ; Marsh, P.; Jančić-Stefanović, J.; Klein, C.; Djurić, M.; Romac, S. | |
| 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 |
| 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 |