Researchers

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Date Issued:  [2000 TO 2009]

Results 1-20 of 25

Issue DateTitleAuthor(s)TypeМ-cat.
2009Mutational analysis of GJB1, MPZ, PMP22, EGR2, and LITAF/SIMPLE in Serbian Charcot-Marie-Tooth patientsKeckarević-Marković, Milica  ; Milić-Rašić, Vedrana  ; Mladenović, Jelena; Dacković, Jelena; Kecmanović, Miljana  ; Keckarević, Dušan  ; Savić-Pavićević, Dušanka  ; Romac, Stanka Article
21M21
2009Congenital cataracts facial dysmorphism neuropathy in Serbian Romani patientsKeckarević-Marković, Milica  ; Milić-Rašić, Vedrana M.  ; Kecmanović, Miljana  ; Keckarević, Dušan P.  ; Romac, Stanka Conference Paper
Mp. category will be shown later
2009Coexistence of Unverricht-Lundborg disease and congenital deafness - molecular resolution of a complex comorbidityKecmanović, Miljana  ; Ristić, Aleksandar J.  ; Sokić, Dragoslav  ; Keckarević-Marković, Milica  ; Vojvodić, Nikola; Ercegovac, Marko  ; Janković, Slavko; Keckarević, Dušan  ; Savić-Pavićević, Dušanka  ; Romac, Stanka Article
21M21
2008Mutations in NHLRC1 gene are predominant cause of Lafora disease in Serbian populationKecmanović, Miljana  ; Jović, N.; Keckarević Marković, Milica  ; Dobričić, Valerija; Keckarević, Dušan  ; Ignjatović, P.; Romac, StankaConference Paper
Mp. category will be shown later
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.Conference Paper
Mp. category will be shown later
2008A three generation Serbian family with C263T mutation in MPZ geneKeckarević-Marković, Milica  ; Dačković, J.; Mladenović, J.; Kecmanović, Miljana  ; Keckarević, Dušan  ; Milić-Rašić, V.; Romac, S.Conference Paper
Mp. category will be shown later
2008Coexistence of Unvericht-Lundborg disease and congenital deafness in one Serbian familyKecmanović, Miljana  ; Ristić, A.; Sokić, D.; Keckarević-Marković, Milica  ; Keckarević, Dušan  ; Romac, S.Conference Paper
Mp. category will be shown later
2008A novel 9-bp duplication in the connexin 32 gene causing X-linked Charcot-Marie-Tooth diseaseKeckarević-Marković, Milica  ; Milić-Rašić, Vedrana M.  ; Kecmanović, Miljana  ; Keckarević, Dušan P.  ; Todorović, Slobodanka; Romac, Stanka Conference Paper
Mp. category will be shown later
2008HD phenocopies - Possible role of saitohin gene (✓)Janković, N.; Kemanović, M.  ; Dimitrijević, Rajna  ; Keckarević-Marković, Milica  ; Dobričić, Valerija; Savić-Pavićević, Dušanka  ; Keckarević, D.  ; Romac, StankaArticle
23M23
2007Hereditary motor and sensory neuropathy type Lom in Serbian Romany familyKeckarević-Marković, Milica  ; Milić-Rašić, Vedrana; Dobricić, Valerija; Kecmanović, Miljana M.  ; Dimitrijević, Rajko ; Sarić, M.; Savić-Pavićević, Dušanka  ; Keckarević, Dušan  ; Todorović, Slobodanka; Romac, StankaConference Paper
Mp. category will be shown later
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.Conference Paper
Mp. category will be shown later
2007Frequency of the hemochromatosis gene mutations in patients with hereditary hemochromatosis and in control subjects from serbia and montenegroŠarić, M.; Zamurović, Lj.; Kečkarević-Marković, M.  ; Kečkarević, Dušan  ; Kecmanović, Miljana  ; Savić-Pavićević, Dušanka  ; Jović, J.; Romac, Stanka Conference Paper
Mp. category will be shown later
2007Human Y-specific STR haplotypes in population of Serbia and MontenegroStevanović, Miljana  ; Dobričić, Valerija; Keckarević, Dušan  ; Perović, Aleksandar; Savić Pavićević, Dušanka  ; Keckarević Marković, Milica  ; Jovanović, Aleksandar; Romac, StankaArticle
21M21
2007Unverricht-Lundborg disease - the first report of genetically confirmed case in SerbiaKecmanović, Miljana M.  ; Ercegovac, Maja  ; Dimitrijević, Rajko ; Dobricic, Valerija; Keckarević-Marković, Milica  ; Savić-Pavićević, Dušanka  ; Keckarević, Dušan  ; Sarić, M.; Bumbaširević, Ljiljana ; Romac, StankaConference Paper
Mp. category will be shown later
2006Clinical case report atypical myopathy in a young girl with 91 CTG repeats in DM1 locus and a positive DM1 family historySavić, Dušanka  ; Keckarević, Dušan  ; Branković-Srećković, Vesna; Apostolski, Slobodan; Todorović, Slobodanka; Romac, StankaArticle
23M23
2006Frequency of the hemochromatosis gene mutations in the population of Serbia and Montenegro (✓)Šarić, M.; Zamurović, Ljubica; Keckarević-Marković, Milica  ; Keckarević, Dušan P.  ; Stevanović, Milena  ; Savić-Pavićević, Dušanka  ; Jović, Jasna; Romac, StankaOther
Mp. category will be shown later
2005Population 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, StankaArticle
21M21
2005Friedreich’s ataxia: analysis of mitotic instabilityDobričić, V.; Keckarević-Marković, Milica  ; Stevanović, M.; Šarić, M.; Savić, D.; Keckarević, Dušan  ; Romac, S.Conference Paper
Mp. category will be shown later
2005Parentalna dijagnostikaRomac, Stanka; Savić-Pavićević, Dušanka  ; Keckarević, Dušan  ; Keckarević-Marković, Milica  Article
Mp. category will be shown later
2005Molekularna osnova spinalnih mišićnih atrofijaKeckarević, Dušan  Conference Paper
Mp. category will be shown later

Results 1-20 of 25