Researchers
Milić-Rašić, Vedrana
Results 61-80 of 84
| Issue Date | Title | Author(s) | Type | Мp-cat. |
|---|---|---|---|---|
| 2012 | Loss-of-function mutations in HINT1 cause axonal neuropathy with neuromyotonia | Zimoń, 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
| Article | 21a+M21a+ |
| 2012 | Neuromuscular disorders and bone mineral density | Dina Vojinović; Milić-Rašić, Vedrana | Conference Paper | Mp. category will be shown later |
| 2012 | Simpozijum Klinicke neurofiziologije | Dina Vojinović; Milić-Rašić, Vedrana | Conference Paper | Mp. category will be shown later |
| 2012 | Neurofiziološke i kliničke karakteristike neuromiotonije u novoj neuromišićnoj bolesti | Milić-Rašić, Vedrana | Conference Paper | Mp. category will be shown later |
| 2011 | Neuromyotonia as a main sign of a possible new type of hereditary axonal neuropathy Neurophysiologic and clinical characteristic of neuromyotonia in new hereditary neuromuscular disorder | Milić-Rašić, Vedrana | Conference Paper | Mp. category will be shown later |
| 2011 | P5.18 Electromyography findings in family with cerebellar ataxia and new genotype | Milić Rašić, Vedrana | Article | 21M21 |
| 2011 | Epidemiology of Charcot-Marie-Tooth disease in the population of Belgrade, Serbia | Mladenovic, J.; Milić Rašić, Vedrana | Article | 21M21 |
| 2011 | Rehabilitation possibility depends on electromyography and genotype in hereditary neuropathy | Milić-Rašić, Vedrana | Conference Paper | Mp. category will be shown later |
| 2011 | Direct detection of DMD/BMD carriers by quantitative real-time PCR![]() | Maksimović, Nela | Conference Paper | Mp. category will be shown later |
| 2011 | Elekromiografija kao dijagnostička procedura kod recesivnih cerebelarnih ataksija | Milić-Rašić, Vedrana | Conference Paper | Mp. category will be shown later |
| 2011 | Serbian serie of congenital myasthenic syndromes (CMS): Correlation between phenotype and genotype | Milić-Rašić, Vedrana | Conference Paper | Mp. category will be shown later |
| 2011 | Rehabilitation possibility depends on electromyography and genotype in hereditary neuropathy | Matanović, Dragana | Article | 21M21 |
| 2011 | Genetic testing for Friedreich's ataxia: first experience from clinic of neurology, clinical center of Serbia | Valerija Dobričić; Milena Janković; Novaković, Ivana | Conference Paper | Mp. category will be shown later |
| 2011 | Kvalitet života osoba sa invaliditetom i ljudska prava | Milić-Rašić, Vedrana | Conference Paper | Mp. category will be shown later |
| 2011 | Genetika spinalnih mišićnih atrofija | Todorović S; Milić-Rašić, Vedrana | Conference Paper | Mp. category will be shown later |
| 2011 | Oculomotor nerve palsy secondary to intracavernous sinus arachnoid cyst in a child-case report | Milić-Rašić, Vedrana | Conference Paper | Mp. category will be shown later |
| 2011 | Genetička osnova kongenitalnih mijasteničnih sindroma | Milić-Rašić, Vedrana | Conference Paper | Mp. category will be shown later |
| 2010 | N88S mutation in the BSCL2 gene in a Serbian family with distal hereditary motor neuropathy type V or Silver syndrome | Rakočević-Stojanović, V.; Milić Rašić, Vedrana | Article | 22M22 |
| 2010 | Targeted Next-Generation Sequencing of a 12.5 Mb Homozygous Region Reveals ANO10 Mutations in Patients with Autosomal-Recessive Cerebellar Ataxia | Vermeer, 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
| Article | 21a+M21a+ |
| 2010 | Autoimmune myasthenia gravis: the youngest patient diagnosed in Serbia | Milić-Rašić, Vedrana | Conference Paper | Mp. category will be shown later |
