Researchers
Kecmanović, Miljana
Results 61-80 of 101
| Issue Date | Title | Author(s) | Type | Мp-cat. |
|---|---|---|---|---|
| 2016 | Single Nucleotide Polymorphisms of Antioxidant Enzymes in Progressive Myoclonus Epilepsy | Ercegovac, Marko D.   ; Jović, Nebojša J. ; Sokić, Dragoslav V. ; Simić, Tatjana P. ; Savić-Radojević, Ana R. ; Ćorić, Vesna M. ; Smiljić, Jelena; Nikolić, Dimitrije M. ; Kecmanović, Miljana ; Plješa-Ercegovac, Marija S. | Conference Paper | Mp. category will be shown later |
| 2015 | Clinical and genetic data on Lafora disease patients of Serbian/Montenegrin origin | Kecmanović, Miljana ; Jović, Nebojša ; Keckarević Marković, Milica ; Keckarević, Dušan ; Stevanović, G.; Ignjatović, P.; Romac, S. | Article | 21M21 |
| 2015 | Is adjunctive perampanel an option for intractable seizures in Lafora disease? | Genton P; Jović, Nebojša ; Lesca G; Kecmanović, Miljana | Article | 21aM21a |
| 2015 | The role of glutathione S-transferases in susceptibility to progressive myoclonus epilepsy | Plješa Ercegovac, Marija S. ; Simić, Tatjana P. ; Ercegovac, Marko D. ; Jović, Nebojša ; Sokić, Dragoslav V. ; Savić-Radojević, Ana R. ; Kecmanović, Miljana M. ; Ćorić, Vesna M. ; Radić, Tanja M. ; Matić, Marija G. | Conference Paper | 34  MNO za medicinske nauke (12.06.2024.)M34 |
| 2015 | GSTA1, GSTM1, GSTP1 and GSTT1 polymorphisms in progressive myoclonus epilepsy: A Serbian case-control study | Ercegovac, Marko ; Jović, Nebojša ; Sokić, Dragoslav ; Savić-Radojević, Ana ; Ćorić, Vesna ; Radić, Tanja ; Nikolić, Dimitrije ; Kecmanović, Miljana ; Matić, Marija ; Simić, Tatjana ;
Plješa-Ercegovac, Marija
; | Article | 22M22 |
| 2014 | Analysis of hexanucleotide GGGGCC repeats in the first intron of the C9orf72 gene | Keckarević, Dušan ; Keckarević-Marković, Milica ; Kecmanović, Miljana ; Stanka Romac | Conference Paper | Mp. category will be shown later |
| 2014 | A shared haplotype indicates a founder event in Unverricht-Lundborg disease patients from Serbia | Kecmanović, Miljana ; Ristić, Aleksandar ; Ercegovac, Marko ; Keckarević-Marković, Milica ; Keckarević, Dušan ; Sokić, Dragoslav ; Romac, Stanka | Article | 23M23 |
| 2014 | Microsatellite analysis in CMT1A genetic testing | Gagić Milica; Keckarević-Marković, Milica ; Keckarević, Dušan ; Kecmanović, Miljana ; Jelena Mladenović; Milić-Rašić, Vedrana ; Stanka Romac | Conference Paper | Mp. category will be shown later |
| 2014 | GSTT1-null genotype influences risk and oxidative phenotype in progressive myoclonus epilepsy | Ercegovac, Marko D. ; N. Jović; Sokić, Dragoslav V. ; Savić-Radojević, Ana R. ; Ćorić, Vesna M. ; Radić, Tanja M. ; Nikolić, Dimitrije M. ; Kecmanović, Miljana M. ; Matić, Marija G. ; Simić, Tatjana P. ;
Plješa Ercegovac, Marija S.
; | Conference Paper | 34 MNO za medicinske nauke (12.06.2024.)M34 |
| 2014 | Molecular genetics of idiopathic generalized epilepsies | Kecmanović, Miljana | Conference Paper | Mp. category will be shown later |
| 2014 | Deletion of NHLRC1 gene is founder mutation in Lafora disease patients of Serbian/Montenegrim origin | Kecmanović, Miljana ; Jović, Nebojša ; Keckarević-Marković, Milica ; Keckarević, Dušan ; Stevanović G; Stanka Romac | Conference Paper | Mp. category will be shown later |
| 2014 | PALM-LCM in sexual assault cases | Kecmanović, Miljana ; Keckarević, Dušan ; Keckarević-Marković, Milica | Conference Paper | Mp. category will be shown later |
| 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. | Conference Paper | Mp. category will be shown later |
| 2013 | An algorithm for genetic testing of serbian patients with demyelinating charcot-marie-tooth | Keckarević Marković, Milica ; Dačković, Jelena; Mladenovic, Jelena; Milić Rašić, Vedrana ; Kecmanović, Miljana ; Keckarević, Dušan ; Romac, Stanka | Article | 23M23 |
| 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 | Article | 22M22 |
| 2012 | Over-representation of the L144F SOD1 mutation in Serbian ALS patients due to founder effect | Keckarevic, Dusan P ; Stevic, Zorica D; Keckarevic-Markovic, Milica ; Kecmanovic, Miljana ; Romac, Stanka P | Conference Paper | Mp. category will be shown later |
| 2012 | Glutathione transferase polymorphism in patients with progressive myoclonic epilepsy | Ercegovac, Marko D. ; Ćorić, Vesna M. ; Simić, Tatjana P. ; N. Jović; Sokić, Dragoslav V. ; Jakovljević, Jovana V. ; Kecmanović, Miljana M. ; Nikolić, Dimitrije M. ; S. Janković; Savić-Radojević, Ana R. ;
Plješa Ercegovac, Marija S.
; | Conference Paper | 34 MNO za medicinske nauke (12.06.2024.)M34 |
| 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 | 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. | Conference Paper | Mp. category will be shown later |
| 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 |