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Keckarević-Marković, Milica

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Full Name
Keckarević-Marković, Milica
Main Affiliation
 
Email
milica@bio.bg.ac.rs
 
ORCID
 
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Publications

Results 51-75 of 99 (Search time: 0.007 seconds).

Issue DateTitleAuthor(s)Rank
5125-Jun-2013Quality of life in patients with Charcot-Marie- Tooth disease in population of BeolgradeMladenović, J.; Milić-Rasić, V.; Keckarević-Marković, Milica ; Romac, S.; Todorović, S.; Rakočević Stojanović, V.; Kisić Tepavčević, D.; Hofman, A.; Pekmezović, T.M34
5225-Jun-2013CCFDN in Serbian patients-does uniform genotypes mean uniform phenotype?Nikodinović Glumac, J.; Milić-Rasić, V.; Keckarević-Marković, Milica ; Mladenović, J.M34
5325-Jun-2013Mutations in PMP22, MPZ0 and GJB1 in Serbian CMT patients: phenotypes and mechanisms of pathogenicityKeckarević-Marković, Milica ; Kecmanović, Miljana ; Keckarević, Dušan ; Dacković, J.; Mladenović, J.; Milić-Rasić, V.; Romac, S.M34
5425-Jun-2013Clinical and neurophysiologic charactersitics of HINT1 neuropathy in Serbian patientsMilić-Rasić, M.; Nikodinović, J.; Mladenović, J.; Jordanova, A.; Baets, J.; Zimon, M.; De Jonghe, P.; Keckarević-Marković, Milica ; Todorović, S.M34
5515-Feb-2013Lafora disease: Severe phenotype associated with homozygous deletion of the NHLRC1 geneKecmanović, Miljana ; Jović, Nebojša; Čukić, Mirjana; Keckarević Marković, Milica ; Keckarević, Dušan ; Stevanović, Galina; Romac, Stanka
56Jan-2013An algorithm for genetic testing of serbian patients with demyelinating charcot-marie-toothKeckarević Marković, Milica P. ; Dackovic, Jelena; Mladenovic, Jelena; Milic-Rasic, Vedrana; Kecmanović, Miljana ; Keckarević, Dušan ; Romac, Stanka
572013Rabdomioliza kao dijagnostički i terapijski izazov kod hereditarne neuropatije sa kongenitalnom kataraktom i facijalnim dismorfizmomNikodinović Glumac, J.; Milić Rašić, V.; Keckarević-Marković, Milica ; Milenković, S.M64
588-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
598-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
608-Sep-2012Over- representation of the L144F SOD1mutation in Serbian ALS patients due tofounder effectKeckarević, Dušan ; Stević, Z.; Keckarević-Marković, Milica ; Kecmanović, Miljana ; Romac, S.M34
619-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
62Feb-2012A novel P66S mutation in exon 3 of the SOD1 gene with early onset and rapid progressionKeckarević, Dušan ; Stević, Zorica; Keckarević Marković, Milica ; Kecmanović, Miljana ; Romac, Stanka
632012Neurofiziološke i kliničke karakteristike neuromiotonije u novoj neuromišićnoj bolestiMilić-Rašić, M.; Nikodinović, J.; De Jonghe, P.; Jordanova, A.; Baets, J.; Zimon, M.; Keckarević-Marković, Milica ; Savić-Pavićević, Dušanka ; Todorović, S.M64
641-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.
65Jul-2010Polymorphisms of the prion protein gene (PRNP) in a Serbian populationDimitrijević, Rajna; Čadež, Ivana; Keckarević Marković, Milica ; Keckarević, Dušan ; Kecmanović, Miljana ; Dobričić, Valerija; Savić Pavićević, Dušanka ; Brajušković, Goran ; Romac, Stanka
66Jul-2010Schizophrenia and apolipoprotein e gene polymorphism in Serbian populationKecmanović, Miljana ; Dobričić, Valerija; Dimitrijević, Rajna; Keckarević, Dušan ; Savić Pavićević, Dušanka ; Keckarević Marković, Milica ; Ivkovic, Maja; Romac, Stanka
6720-Jun-2009Congenital cataracts facial dysmorphism neuropathy in Serbian Romani patientsKeckarević-Marković, Milica ; Milić-Rašić, V.; Kecmanović, Miljana ; Keckarević, Dušan ; Romac, S.M34
68Jun-2009Mutational analysis of GJB1, MPZ, PMP22, EGR2, and LITAF/SIMPLE in Serbian Charcot-Marie-Tooth patientsKeckarević Marković, Milica ; Milic-Rasic, Vedrana; Mladenovic, Jelena; Dackovic, Jelena; Kecmanović, Miljana ; Keckarević, Dušan ; Savić Pavićević, Dušanka ; Romac, Stanka
69Jun-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
702009&Molekularna analiza Gli3 gena kod pacijenata sa Palister-Halovim sindromomRadivojević, M.; Keckarević-Marković, Milica ; Dačković, J.; Apostolski, S.; Brajušković, Goran ; Romac, S.M64
71Oct-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.
727-Jun-2008A novel 9-bp duplication in the connexin 32 gene causing X-linked Charcot-Marie-Tooth diseaseKeckarević-Marković, Milica ; Milić-Rašić, V.; Kecmanović, Miljana ; Keckarević, D.; Todorović, S.; Romac, S.M34
737-Jun-2008Mutations in NHLRC1 gene are predominant cause of Lafora disease in Serbian populationKecmanović, Miljana ; Jović, N.; Keckarević-Marković, Milica ; Dobričić, V.; Keckarević, Dušan ; Ignjatović, P.; Romac, S.M34
7431-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
7531-May-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.M34