Browsing eNauka

Browsing by Author Mladenović, J.

Showing results 1 to 13 of 13
Issue DateTitleAuthor(s)TypeМp-cat.
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
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2019ARCA3 in Serbian Romani family caused by founder mutation in ANO10 – a genetic approacMihajlović, M.; Tanasić, V.; Keckarević, Dušan  ; Mladenović, J.; Kecmanović, Miljana  ; Keckarević-Marković, Milica  Conference Paper
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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.Conference Paper
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2023Detekcija markera uboda krpelja u serumu dobrovoljnih davalaca krviMihaljica, D.; Marković, D.; Božić Nedeljković, B.  ; Veinović, G.; Sukara, R.; Vučetić, D.; Krstić, M.; Mladenović, J.; Atanasievska, S.; Protić Đokić, V.;
Đorđevski, N.; Ristanović, E.; Tomanović, S.;
Conference Paper
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2015Elevated level of creatinine phosphokinase in the blood of patients with peripheral polyneuropathiesMladenović, J.; Glumac, J. Nikodinović; Kosać, A.; Keckarević Marković, Milica  ; Baets, J.; Milić Rašić, Vedrana Conference Paper
21M21
2012Founder R32G mutation in GJB1 gene of Serbian CMT patientsKeckarević-Marković, Milica  ; Kecmanović, Miljana  ; Keckarević, Dušan  ; Mladenović, J.; Milić-Rasić, V.; Romac, S.Conference Paper
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2015Is it easy to recognize HINT1 neuropathy (oral presentation)Milić Rašić, V.; Branković, V.; Mladenović, J.; Nikodinović, J.; Kosac, A.; Baets, J.; De Jonghe, P.; Jordanova, A.; Zimon, M.; Keckarević-Marković, Milica  ;
Savić-Pavićević, Dušanka  ; Todorović, S.;
Conference Paper
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2012Molecular genetics of myotonic disorders in Serbian patientsSavić-Pavićević, Dušanka  ; Milić Rašić, V.; Mladenović, J.; Rakočević Stojanović, V.; Brajušković, Goran  ; Jordanova, A.; De Jonghe, P.; Todorović, S.; Romac, S.Conference Paper
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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.Conference Paper
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2023Novel multiplex SnaPShot reaction designed for detection of eight founder mutation associated with single-gene disorders in Serbian Roma populationTanasić, V.; Mihajlović Srejić, M.; Mladenović, J.; Kecmanović, Miljana  ; Keckarević-Marković, Milica  ; Keckarević, Dušan  Conference Paper
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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.Conference Paper
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2012The advancement of molecular diagnostics of CMT in SerbiaKeckarević-Marković, Milica  ; Milić-Rašić, V.; Mladenović, J.; Dačković, J.; Kecmanović, Miljana  ; Keckarević, Dušan  ; Romac, S.Conference Paper
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2018The golden jackal in Europe: Where to go next?Ranc, N.; Álvares, F.; Banea, O.C.; Berce, T.; Caganacci, F.; Červinka, J.; Ćirović, Duško S.  ; Cosic, N.; Giannatos, G.,; Hatlauf, J.;
Heltal, M.; Hosting, Z.; Ivanov, G.; Lanzski, J.; Lapini, L.; Maiorano, L.; Melovski, D.; Migli, D.; Mladenović, J.; Pankov, I.A.; Penezić, A.  ; Petrova, A.  ; Šálek, M.; Selanec, I.; Selimović, A.; Sforna, T.; Stojanov, A.; Szabó, L.; Trbojević, I.; Trbojević, T.; Krofel, M.;
Conference Paper
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