Researchers
Keckarević, Dušan
Results 81-100 of 113
| Issue Date | Title | Author(s) | Type | Мp-cat. |
|---|---|---|---|---|
| 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 | Article | 21M21 |
| 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. | Conference Paper | Mp. category will be shown later |
| 2012 | SOD1, ANG, TARDBP mutations and ATXN2 trinucleotide repeat variations in ALS patients from Serbia | Milena Milićev; Stević, Zorica ; Keckarević, Dušan ; Keckarević Marković, Milica ; Stevanović, Mirna; Romac S | Conference Paper | Mp. category will be shown later |
| 2011 | Molekularno genetička osnova amiotrofične lateralne skleroze kod pacijenata u populaciji Srbije | Keckarević, Dušan | Doctoral theses | 70M70 |
| 2011 | Eksperimentalna biohemija : praktikum | Radović, Svetlana ; Lozo, Jelena ; Keckarević, Dušan | Text book | Mp. category will be shown later |
| 2011 | Mutacija gena za SOD1, TARDBP1 i angiogenin kod bolesnika sa amiotrofičnom lateralnom sklerozom: genotipsko-fenotipske karakteristike | Lavrnić, Dragana ; Rakočević-Stojanović, Vidosava ; Stević, Zorica ; Keckarević, Dušan ; Basta, Ivana ; Ivan Marjanović; Stanka Romac; Perić, Stojan | Conference Paper | Mp. category will be shown later |
| 2010 | Polymorphisms of the Prion Protein Gene (PRNP) in a Serbian Population | Dimitrijević, Rajna ; Cadez, Ivana; Keckarević-Marković, Milica ; Keckarević, Dušan ; Kecmanović, Miljana ; Dobričić, Valerija; Savić-Pavićević, Dušanka ; Brajusković, Goran ; Romac, Stanka | Article | 23M23 |
| 2010 | Schizophrenia and Apolipoprotein E Gene Polymorphism in Serbian Population | Kecmanović, Miljana ; Dobričić, Valerija; Dimitrijević, Rajna ; Keckarević, Dušan ; Savić-Pavićević, Dušanka ; Keckarević-Marković, Milica ; Ivković, Maja ; Romac, Stanka | Article | 23M23 |
| 2009 | Mutational analysis of GJB1, MPZ, PMP22, EGR2, and LITAF/SIMPLE in Serbian Charcot-Marie-Tooth patients | Keckarević-Marković, Milica ; Milić-Rašić, Vedrana ; Mladenović, Jelena; Dacković, Jelena; Kecmanović, Miljana ; Keckarević, Dušan ; Savić-Pavićević, Dušanka ; Romac, Stanka | Article | 21M21 |
| 2009 | Congenital cataracts facial dysmorphism neuropathy in Serbian Romani patients | Keckarević-Marković, Milica ; Milić-Rašić, Vedrana M. ; Kecmanović, Miljana ; Keckarević, Dušan P. ; Romac, Stanka | Conference Paper | Mp. category will be shown later |
| 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 | Article | 21aM21a |
| 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. | Conference Paper | Mp. category will be shown later |
| 2008 | Mutations in NHLRC1 gene are predominant cause of Lafora disease in Serbian population | Kecmanović, Miljana ; Jović, N.; Keckarević Marković, Milica ; Dobričić, Valerija; Keckarević, Dušan ; Ignjatović, P.; Romac, Stanka | Conference Paper | Mp. category will be shown later |
| 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. | Conference Paper | Mp. category will be shown later |
| 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. | Conference Paper | Mp. category will be shown later |
| 2008 | HD phenocopies - Possible role of saitohin gene | Janković, N.; Kemanović, M. ; Dimitrijević, Rajna ; Keckarević-Marković, Milica ; Dobričić, Valerija; Savić-Pavićević, Dušanka ; Keckarević, D. ; Romac, Stanka | Article | 23M23 |
| 2008 | A novel 9-bp duplication in the connexin 32 gene causing X-linked Charcot-Marie-Tooth disease | Keckarević-Marković, Milica ; Milić-Rašić, Vedrana M. ; Kecmanović, Miljana ; Keckarević, Dušan P. ; Todorović, Slobodanka; Romac, Stanka | Conference Paper | Mp. category will be shown later |
| 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 | Article | 21M21 |
| 2007 | Hereditary motor and sensory neuropathy type Lom in Serbian Romany family | Keckarević-Marković, Milica ; Milić-Rašić, Vedrana; Dobricić, Valerija; Kecmanović, Miljana M. ; Dimitrijević, Rajko ; Sarić, M.; Savić-Pavićević, Dušanka ; Keckarević, Dušan ; Todorović, Slobodanka; Romac, Stanka | Conference Paper | Mp. category will be shown later |
| 2007 | Unverricht-Lundborg disease - the first report of genetically confirmed case in Serbia | Kecmanović, Miljana M. ; Ercegovac, Maja ; Dimitrijević, Rajko ; Dobricic, Valerija; Keckarević-Marković, Milica ; Savić-Pavićević, Dušanka ; Keckarević, Dušan ; Sarić, M.; Bumbaširević, Ljiljana ; Romac, Stanka | Conference Paper | Mp. category will be shown later |