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



Refined By:
Author:  Keckarević-Marković, Milica
Date Issued:  [2010 TO 2019]
Date Issued:  2013

Results 1-7 of 7 (Search time: 0.049 seconds).

Issue DateTitleAuthor(s)Rank
125-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
225-Jun-2013CCFDN in Serbian patients-does uniform genotypes mean uniform phenotype?Nikodinović Glumac, J.; Milić-Rasić, V.; Keckarević-Marković, Milica ; Mladenović, J.M34
325-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
425-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
515-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
6Jan-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
72013Rabdomioliza 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