Keckarević, Dušan
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Full Name
Keckarević, Dušan
Main Affiliation
Email
duskec@bio.bg.ac.rs
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Results 1-19 of 19 (Search time: 0.01 seconds).
| Issue Date | Title | Author(s) | Rank | |
|---|---|---|---|---|
| 1 | 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 |
| 2 | 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 | |
| 3 | 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 | |
| 4 | 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 |
| 5 | 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 |
| 6 | 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 |
| 7 | 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 |
| 8 | 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. | |
| 9 | 13-Sep-2007 | Human Y-specific STR haplotypes in population of Serbia and Montenegro | Stevanović, Miljana ; Dobričić, Valerija; Keckarević, Dušan ; Perović, Aleksandar; Savić Pavićević, Dušanka ; Keckarević Marković, Milica ; Jovanović, Aleksandar; Romac, Stanka | |
| 10 | 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 |
| 11 | 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 |
| 12 | 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 |
| 13 | Aug-2006 | Frequency of the hemochromatosis gene mutations in the population of Serbia and Montenegro [2] | Šarić, M.; Zamurović, Lj; Keckarević Marković, M. ; Keckarević, D. ; Stevanović, M. ; Savić Pavićević, D. ; Jović, J.; Romac, Stanka | |
| 14 | 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 |
| 15 | 16-Jul-2005 | Population data on 14 STR loci from population of Serbia and Montenegro (new and renewed data) | Keckarević, Dušan ; Savić, Dušanka ; Keckarević, Milica ; Stevanović, Miljana ; Tarasjev, Aleksej; Čuljković, Biljana; Darmati, Ana; Vukosavić, Slobodanka; Romac, Stanka | |
| 16 | 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 |
| 17 | Oct-2002 | Genetic and clinical analysis of spinocerebellar ataxia type 8 repeat expansion in Yugoslavia | Topisirovic, I.; Dragaševic, N.; Savic, D. ; Ristic, A.; Keckarevic, M. ; Keckarevic, D. ; Culjkovic, B.; Petrovic, I.; Romac, S.; Kostic, V. S. | |
| 18 | May-2002 | Duchenne's and Becker's muscular dystrophy: analysis of phenotype-genotype correlation in 28 patients] | Keckarević, Milica ; Savić, Dušanka ; Culjković, Biljana; Zamurović, Natasa; Major, Tamara; Keckarević, Dušan ; Todorović, Slobodanka; Romac, Stanka | |
| 19 | 1-Dec-2001 | Is the 31 CAG repeat allele of the spinocerebellar ataxia 1 (SCA1) gene locus non-specifically associated with trinucleotide expansion diseases? | Savić, Dušanka ; Topisirović, Ivan; Keckarević, Milica ; Keckarević, Dušan ; Major, Tamara; Čuljković, Biljana; Stojković, Oliver; Rakočević-Stojanović, Vidosava; Mladenović, Jelena; Todorović, Slobodanka; Apostolski, Slobodan; Romac, Stanka |