Researchers



Results 61-80 of 84
Issue DateTitleAuthor(s)TypeМp-cat.
2012Loss-of-function mutations in HINT1 cause axonal neuropathy with neuromyotoniaZimoń, Magdalena; Baets, Jonathan; Almeida-Souza, Leonardo; De, Vriendt Els; Nikodinovic, Jelena; Parman, Yesim; Battaloǧlu, Esra; Matur, Zeliha; Guergueltcheva, Velina; Tournev, Ivailo;
Auer-Grumbach, Michaela; De, Rijk Peter; Petersen, Britt-Sabina; Müller, Thomas; Fransen, Erik; Van, Damme Philip; Löscher, Wolfgang N; Barišić, Nina; Mitrovic, Zoran; Previtali, Stefano C; Topaloǧlu, Haluk; Bernert, Günther; Beleza-Meireles, Ana; Todorovic, Slobodanka; Savić Pavićević, Dušanka  ; Ishpekova, Boryana; Lechner, Silvia; Peeters, Kristien; Ooms, Tinne; Hahn, Angelika F; Züchner, Stephan; Timmerman, Vincent; Van, Dijck Patrick; Milić Rašić, Vedrana ; Janecke, Andreas R; De, Jonghe Peter; Jordanova, Albena;
Article
21a+M21a+
2012Neuromuscular disorders and bone mineral densityDina Vojinović; Milić-Rašić, Vedrana ; Kosac A; Susic G; Todorovic SConference Paper
Mp. category will be shown later
2012Simpozijum Klinicke neurofiziologijeDina Vojinović; Milić-Rašić, Vedrana Conference Paper
Mp. category will be shown later
2012Neurofiziološke i kliničke karakteristike neuromiotonije u novoj neuromišićnoj bolestiMilić-Rašić, Vedrana ; Nikodinovic J; Mladenovic J; De Jonghe P; Jordanova A; Baets J; Zimon M; Keckarevic Markovic M; Savic Pavicevic D; Todorovic SConference Paper
Mp. category will be shown later
2011Neuromyotonia as a main sign of a possible new type of hereditary axonal neuropathy Neurophysiologic and clinical characteristic of neuromyotonia in new hereditary neuromuscular disorderMilić-Rašić, Vedrana ; Todorovic S; Nikodinovic J; Mladenovic J; De Jonghe P; Jordanova A; Baets J; Zimon M; Keckarević Marković, Milica  ; Brankovic VConference Paper
Mp. category will be shown later
2011P5.18 Electromyography findings in family with cerebellar ataxia and new genotypeMilić Rašić, Vedrana ; Todorovic, S.; Brankovic, V.; Matanović, Dragana  ; Vermeer, S.Article
21M21
2011Epidemiology of Charcot-Marie-Tooth disease in the population of Belgrade, SerbiaMladenovic, J.; Milić Rašić, Vedrana ; Keckarević Marković, Milica  ; Romac, S.; Todorovic, S.; Stojanović, Vidosava ; Kisic, Tepavcevic D.  ; Hofman, A.; Pekmezović, Tatjana  Article
21M21
2011Rehabilitation possibility depends on electromyography and genotype in hereditary neuropathyMilić-Rašić, Vedrana ; Matanović, Dragana  Conference Paper
Mp. category will be shown later
2011Direct detection of DMD/BMD carriers by quantitative real-time PCRMaksimović, Nela  ; Anđelković, Ana; Rašić-Milić, Vedrana ; Todorović, Slobodanka ; Luković, Ljiljana ; Dobričić, Valerija ; Damnjanović, Tatjana  ; Perović, Dijana  ; Novaković, Ivana  Conference Paper
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2011Elekromiografija kao dijagnostička procedura kod recesivnih cerebelarnih ataksijaMilić-Rašić, Vedrana ; Todorović S; Branković V; Novaković I; Baets J; Vermeer SConference Paper
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2011Serbian serie of congenital myasthenic syndromes (CMS): Correlation between phenotype and genotypeMilić-Rašić, Vedrana ; Todorovic S; Lochmuller HConference Paper
Mp. category will be shown later
2011Rehabilitation possibility depends on electromyography and genotype in hereditary neuropathyMatanović, Dragana  ; Milić Rašić, Vedrana Article
21M21
2011Genetic testing for Friedreich's ataxia: first experience from clinic of neurology, clinical center of SerbiaValerija Dobričić; Milena Janković; Novaković, Ivana  ; Čuturilo, Goran  ; Dragasevic Miskovic Natasa; Svetel, Marina ; Milić Rašić, Vedrana ; Kostić, Vladimir Conference Paper
Mp. category will be shown later
2011Kvalitet života osoba sa invaliditetom i ljudska pravaMilić-Rašić, Vedrana ; Jovanović M; Jančić, Jasna  ; Slavnić, Svetlana Conference Paper
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2011Genetika spinalnih mišićnih atrofijaTodorović S; Milić-Rašić, Vedrana ; Romac S; Savić Pavićević, Dušanka  Conference Paper
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2011Oculomotor nerve palsy secondary to intracavernous sinus arachnoid cyst in a child-case reportMilić-Rašić, Vedrana ; Pepic A; Nagulic M; Mrvos Cobeljic DusankaConference Paper
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2011Genetička osnova kongenitalnih mijasteničnih sindromaMilić-Rašić, Vedrana ; Todorović S; Lochmuller HConference Paper
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2010N88S mutation in the BSCL2 gene in a Serbian family with distal hereditary motor neuropathy type V or Silver syndromeRakočević-Stojanović, V.; Milić Rašić, Vedrana ; Perić, S.  ; Baets, J.; Timmerman, V.; Dierick, I.; Pavlović, S.; De, Jonghe P.Article
22M22
2010Targeted Next-Generation Sequencing of a 12.5 Mb Homozygous Region Reveals ANO10 Mutations in Patients with Autosomal-Recessive Cerebellar AtaxiaVermeer, Sascha; Hoischen, Alexander; Meijer, Rowdy P.P.; Gilissen, Christian; Neveling, Kornelia; Wieskamp, Nienke; de, Brouwer Arjan; Koenig, Michel; Anheim, Mathieu; Assoum, Mirna;
Drouot, Nathalie; Todorovic, Slobodanka; Milić Rašić, Vedrana ; Lochmüller, Hanns; Stevanin, Giovanni; Goizet, Cyril; David, Albert; Durr, Alexandra; Brice, Alexis; Kremer, Berry; van, de Warrenburg Bart P.C.; Schijvenaars, Mascha M.V.A.P.; Heister, Angelien; Kwint, Michael; Arts, Peer; van, der Wijst Jenny; Veltman, Joris; Kamsteeg, Erik-Jan; Scheffer, Hans; Knoers, Nine;
Article
21a+M21a+
2010Autoimmune myasthenia gravis: the youngest patient diagnosed in SerbiaMilić-Rašić, Vedrana ; Potić Ana; Jančić, Jasna  Conference Paper
Mp. category will be shown later