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Browsing by Author Romac, S.


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Showing results 1 to 20 of 35  next >
Issue DateTitleAuthor(s)Rank
9-Jul-2012The advancement of molecular diagnostics of CMT in SerbiaKeckarević-Marković, Milica ; Milić-Rašić, V.; Mladenović, J.; Dačković, J.; Kecmanović, Miljana ; Keckarević, Dušan ; Romac, S.M34
2005Analiza genskih mutacija kod pacijenata sa naslednim neuropatijamaMilić Rašić, V.; Todorović, S.; Keckarević-Marković, Milica ; Romac, S.M45
2014Analysis of hexanucleotide GGGGCC repeats in the first intron of the C9orf72 geneLabus, O.; Keckarević, Dušan ; Keckarević-Marković, Milica ; Kecmanović, Miljana ; Romac, S.M64
Aug-2015Assessment of association between genetic variants in microRNA genes hsa-miR-499, hsa-miR-196a2 and hsa-miR-27a and prostate cancer risk in Serbian populationNikolić, Z.; Savić Pavićević, Dušanka ; Vučić, Nemanja ; Cidilko, S.; Filipović, N.; Cerović, S.; Vukotić, V.; Romac, S.; Brajušković, Goran 
Jan-2016Clinical and genetic data on Lafora disease patients of Serbian/Montenegrin originKecmanović, Miljana ; Jović, N.; Keckarević Marković, Milica ; Keckarević, Dušan ; Stevanović, G.; Ignjatović, P.; Romac, S.
31-May-2008Coexistence of Unvericht-Lundborg disease and congenital deafness in one Serbian familyKecmanović, Miljana ; Ristić, A.; Sokić, D.; Keckarević-Marković, Milica ; Keckarević, Dušan ; Romac, S.M34
20-Jun-2009Congenital cataracts facial dysmorphism neuropathy in Serbian Romani patientsKeckarević-Marković, Milica ; Milić-Rašić, V.; Kecmanović, Miljana ; Keckarević, Dušan ; Romac, S.M34
2014Deletion of NHLRC1 gene is founder mutation in Lafora disease patients of Serbian/Montenegrim originKecmanović, Miljana ; Jović, N.; Keckarević-Marković, Milica ; Keckarević, Dušan ; Stevanović, G.; Romac, S.M64
1-Jun-2011Epidemiology of Charcot-Marie-Tooth disease in the population of Belgrade, SerbiaMladenovic, J.; Milic Rasic, V.; Keckarević Marković, M. ; Romac, S.; Todorovic, S.; Rakocevic Stojanovic, V.; Kisic Tepavcevic, D.; Hofman, A.; Pekmezovic, T.
8-Sep-2012Founder c.1048-1049delGA mutation in NHLRC1 gene in Lafora’s disease patients from SerbiaKecmanović, Miljana ; Jović, N.; Keckarević-Marković, Milica ; Keckarević, Dušan ; Stevanović, G.; Romac, S.M34
8-Sep-2012Founder R32G mutation in GJB1 gene of Serbian CMT patientsKeckarević-Marković, Milica ; Kecmanović, Miljana ; Keckarević, Dušan ; Mladenović, J.; Milić-Rasić, V.; Romac, S.M34
2-Jul-2006Four years of remission in the first Unverricht- Lundborg case in the Balkan regionErcegovac, M.; Stevanović, M. ; Beslać Bumbasirević, L.; Jovanović, D.; Romac, S.; Ercegovac, D.M34
2007Frequency of the hemochromatosis gene mutations in patients with hereditary hemochromatosis and in control subjects from Serbia and MontenegroŠarić, M.; Zamurović, Lj.; Keckarević-Marković, Milica ; Keckarević, Dušan ; Kecmanović, Miljana ; Savić-Pavićević, Dušanka ; Jović, J.; Romac, S.M34
31-May-2008Frequency of the hemochromatosis gene mutations in patients with hereditary hemochromatosis and in control subjects from SerbiaŠarić, M.; Zamurović, L.; Keckarević-Marković, Milica ; Keckarević, Dušan ; Kecmanović, Miljana ; Savić-Pavićević, Dušanka ; Jović, J.; Romac, S.M34
5-Sep-2005Friedreich’s ataxia: analysis of mitotic instabilityDobričić, V.; Keckarević-Marković, Milica ; Stevanović, M.; Šarić, M.; Savić, D.; Keckarević, Dušan ; Romac, S.M34
Oct-2002Genetic and clinical analysis of spinocerebellar ataxia type 8 repeat expansion in YugoslaviaTopisirovic, I.; Dragaševic, N.; Savic, D. ; Ristic, A.; Keckarevic, M. ; Keckarevic, D. ; Culjkovic, B.; Petrovic, I.; Romac, S.; Kostic, V. S.
1-Dec-2003Genetic study of somatic mosaicism in a patient with myotonic dystrophy type 1: Case reportRakocevic-Stojanovic, Vidosava; Savić Pavićević, Dušanka ; Romac, S.; Apostolski, S.
Mar-2008HD phenocopies - Possible role of saitohin geneJanković, N.; Kecmanović, M. ; Dimitrijević, R.; Keckarević Marković, M. ; Dobričić, V.; Keckarević, D. ; Savić Pavićević, D. ; Romac, S.
Oct-2008Hereditary motor and sensory neuropathy Lom type in a Serbian familyDačković, Jalena; Keckarević-Marković, M. ; Komazec, Z.; Rakočević-Stojanović, V.; Lavrnić, D.; Stević, Z.; Ribarić, K.; Romac, S.; Apostolski, S.
16-Jun-2007Hereditary Motor and Sensory Neuropathy type Lom in Serbian Romani familyKeckarević-Marković, Milica ; Milić-Rašić, V.; Dobričić, V.; Kecmanović, Miljana ; Dimitrijević, R.; Šarić, M.; Savić-Pavićević, Dušanka ; Keckarević, Dušan ; Todorović, S.; Romac, S.M34
Showing results 1 to 20 of 35  next >