Researchers
Keckarević-Marković, Milica
Results 81-100 of 132
| Issue Date | Title | Author(s) | Type | Мp-cat. |
|---|---|---|---|---|
| 2013 | Quality of life in patients with Charcot-Marie- Tooth disease in population of Beolgrade | Mladenović, J.; Milić-Rasić, V.; Keckarević-Marković, Milica   ; Romac, S.; Todorović, S.; Rakočević Stojanović, V.; Kisić Tepavčević, D.; Hofman, A.; Pekmezović, T. | Conference Paper | Mp. category will be shown later |
| 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 |
| 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 |
| 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 |
| 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 | Epidemiology of Charcot-Marie-Tooth disease in the population of Belgrade, Serbia | Mladenovic, J.; Milić Rašić, Vedrana ; Keckarević Marković, Milica ; Romac, S.; Todorovic, S.; Stojanović, Vidosava ; Kisic, Tepavcevic D. ; Hofman, A.; Pekmezović, Tatjana | Article | 21M21 |
| 2011 | Neuromyotonia as a main sign of a possible new type of hereditary axonal neuropathy Neurophysiologic and clinical characteristic of neuromyotonia in new hereditary neuromuscular disorder | Milić-Rašić, Vedrana ; Todorovic S; Nikodinovic J; Mladenovic J; De Jonghe P; Jordanova A; Baets J; Zimon M; Keckarević Marković, Milica ; Brankovic V | Conference Paper | Mp. category will be shown later |
| 2011 | Pallister Hall sindrom: porodica iz Srbije | Dačković, Jelena R.; Radivojević Miloš; Keckarević Marković, Milica P. ; Brajušković, Goran R. ; S. Romac | 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 |
| 2010 | Molekularno genetička osnova hereditarne motorne i senzorne neuropatije tip 1 (HMSN1) kod pacijenata u populaciji Srbije | Keckarević Marković, Milica | Doctoral theses | 70M70 |
| 2009 | &Molekularna analiza Gli3 gena kod pacijenata sa Palister-Halovim sindromom | Radivojević, M.; Keckarević-Marković, Milica ; Dačković, J.; Apostolski, S.; Brajušković, Goran ; Romac, S. | Conference Paper | Mp. category will be shown later |
| 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 |