Researchers



Results 241-260 of 356
Issue DateTitleAuthor(s)TypeМp-cat.
2016Guillain-Barré syndrome and comorbid disordersBjelica, Bogdan ; Božović, Ivo ; Perić, Stojan Z.  ; Berisavac, Ivana I.  ; Beslać-Bumbaširević, Ljiljana ; Lavrnić, Dragana V. ; Stević, Zorica D. Conference Paper
Mp. category will be shown later
2016A novel recessive TTN founder mutation is causing a distal myopathy phenotype in a Serbian patient cohortJ. Nikodinović-Glumac; A. Topf; H. Lochmüller; Savić Pavićević, Dušanka Lj.  ; M. Bertoli; M. Lek; D. MacArthur; L. Xu; Perić, Stojan Z.  ; Milić Rašić, Vedrana M. ;
Brkušanin, Miloš Đ.  ; Milenković, Sanja M.  ; M. Cassop-Thompson; B. Banko; Maksimović, Ružica M.  ; Stojanović, Vidosava M. ; V. Straub;
Conference Paper
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2016Prognostic factors and survival of ALS patients from Belgrade, SerbiaStević, Zorica ; Kostić-Dedić, Svetlana; Perić, Stojan  ; Dedić, Velimir  ; Basta, Ivana  ; Stojanović, Vidosava ; Lavrnić, Dragana Article
22M22
2016Recurrent Guillain-Barre Syndrome - Case SeriesBasta, Ivana Z.  ; Stojiljković, Olivera; Perić, Stojan Z.  ; Lukić, Sonja; Babić, Milica; Komatina, Nenad D.  ; Petrović, Milutin; Vujović, Balša; Stević, Zorica D. ; Lavrnić, Dragana V. Conference Paper
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2016Comparison of temporal and stride characteristics in myotonic dystrophies type 1 and 2 during dual-task walkingRadovanović, Saša M.  ; Perić, Stojan  ; Savić-Pavićević, Dušanka  ; Dobričić, Valerija ; Pešović, Jovan  ; Kostić, Vladimir S. ; Rakočević-Stojanović, Vidosava Article
21aM21a
2016Titin antibodies in seronegative myasthenia gravis — A new role for an old antigenStergiou, C.; Lazaridis, K.; Zouvelou, V.; Tzartos, J.; Mantegazza, R.; Antozzi, C.; Andreetta, F.; Evoli, A.; Deymeer, F.; Saruhan-Direskeneli, G.;
Durmus, H.; Brenner, T.; Vaknin, A.; Berrih-Aknin, S.; Behin, A.; Sharshar, T.; De Baets, M.; Losen, M.; Martinez-Martinez, P.; Kleopa, K.A.; Zamba-Papanicolaou, E.; Kyriakides, T.; Kostera-Pruszczyk, A.; Szczudlik, P.; Szyluk, B.; Lavrnić, Dragana ; Basta, Ivana  ; Perić, Stojan  ; Tallaksen, C.; Maniaol, A.; Gilhus, N.E.; Casasnovas Pons, C.; Pitha, J.; Jakubíkova, M.; Hanisch, F.; Bogomolovas, J.; Labeit, D.; Labeit, S.; Tzartos, S.J.;
Article
22M22
2016Clusters of cognitive impairment among different forms of myotonic dystrophiesPerić, Stojan  ; Mandić-Stojimenović, Gorana  ; Ilić, Vera; Kovačević, Maša ; Parojčić, Aleksandra; Dobričić, Valerija ; Pešović, Jovan  ; Novaković, Ivana  ; Savić-Pavićević, Dušanka  ; Stojanović, Vidosava Conference Paper
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2016Guillain-Barré syndrome in the elderlyPerić, Stojan  ; Berisavac, Ivana  ; Stojiljković-Tamaš, Olivera; Rajić, Sonja  ; Babić, Milica; Cvijanović, Milan ; Dominović-Kovačević, Aleksandra; Basta, Ivana  ; Beslać-Bumbaširević, Ljiljana ; Lavrnić, Dragana Article
21M21
2016Application of exome sequencing technologies: A case study of patients with unexplained limb-girdle muscle weakness harbouring GAA mutationsJohnson, Katherine; Bertoli, Marta; Phillips, Lauren; Töpf, Ana; Claeys, Kristl; Rakočević-Stojanović, Vidosava M. ; Perić, Stojan Z.  ; Vissine, John; Hahn, Andreas; Maddison, Paul;
Akay, Ela; Bastian, Alexandra E.; Lusakowska, Anna; Lek, Monkol; Xu, Liwen; MacArthur, Daniel; Straub, Volker;
Conference Paper
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2016Myopathic changes detected by quantitative electromyography in patients with MuSK and AChR positive myasthenia gravisNikolić, Ana ; Basta, Ivana  ; Stojanović, Vidosava ; Stević, Zorica ; Perić, Stojan  ; Lavrnić, Dragana Article
23M23
2016A recessive TTN founder mutation causes a distal myopathy phenotype in a Serbian cohortTonf, A.; Nikodinović-Glumac, Jelena; Perić, Stojan Z.  ; Cassop-Thompson, M.; Bertoli, M.; Johnson, Katherine; Phillips, L.; MacArthur, D.; Rakočević-Stojanović, Vidosava M. ; Straub, V.Conference Paper
Mp. category will be shown later
2016A recessive TTN founder mutation is causing a distal myopathy phenotype in a Serbian patient cohortPerić, Stojan  ; Nikodinović-Glumac Jelena; Topf A; Lochmüller H; Bertoli M; MacArthur D; Lek M; Xu L; Savić-Pavićević, Dušanka  ; Milenković, Sanja M.  ;
Cassop-Thompson M; Milić Rašić, Vedrana M. ; Stojanović, Vidosava ; Straub V;
Conference Paper
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2016Phenotypic characteristics of titinopathy caused by a founder autosomal recessive mutation in Serbian populationPerić, Stojan  ; Stojanović, Vidosava ; Nikodinović-Glumac Jelena; Topf A; Lochmüller H; Savić-Pavićević, Dušanka  ; Bertoli M; Lek M; MacArthur DG; Xu L;
Milić Rašić, Vedrana ; Brkušanin, Miloš  ; Milenković, Sanja  ; Cassop-Thompson MJ; Straub V;
Conference Paper
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2016Quality of life in patients with myotonic dystrophy type 2Stojanović, Vidosava ; Perić, Stojan  ; Paunić, Teodora; Pešović, Jovan  ; Vujnić, Milorad; Perić, Marina; Nikolić, Ana ; Lavrnić, Dragana ; Savić-Pavićević, Dušanka  Article
22M22
2016Hyperacute Guillain-Barree SyndromeStević, Zorica ; Perić, Stojan Z.  ; Berisavac, Ivana; Đorđević, Gordana  ; Basta, Ivana  ; CVIJANOVIĆ, MILAN ; A. Dominovic; Martić, Vesna  ; Lavrnić, Dragana Conference Paper
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2015Varijabilnost multisistemske afekcije u miotoničnoj distrofiji tip 1 - pouke iz srpskog registraRakočević-Stojanović, Vidosava ; Perić, Stojan  ; Novaković, Ivana  ; Basta, Ivana  ; Nikolić, Ana; Dobričić, Valerija ; Kačar, Aleksandra  ; Marjanović, Ana ; Savić-Pavićević, Dušanka  ; Stević, Zorica ;
Lavrnić, Dragana ;
Conference Paper
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2015Praćenje karakteristika hoda kod bolesnika sa miotoniĉnom distrofijom tipa 1 i 2Radovanović, Saša  ; Perić, Stojan Z.  ; Savić-Pavićević, Dušanka  ; Dobričić, Valerija ; Pešović, Jovan  ; Kostić, Vladimir ; Stojanović, Vidosava Conference Paper
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2015Metabolic syndrome in patients with myotonic dystrophy type 1Vujnić, Milorad; Perić, Stojan  ; Popović, Srđan ; Rašeta, Nela; Ralić, Vesna; Dobričić, Valerija ; Novaković, Ivana  ; Stojanović, Vidosava Article
22M22
2015Frontostriatal dysexecutive syndrome: a core cognitive feature of myotonic dystrophy type 2Perić, Stojan  ; Mandić-Stojmenović, Gorana  ; Stefanova, Elka ; Savić-Pavićević, Dušanka  ; Pešović, Jovan  ; Ilić, Vera; Dobričić, Valerija ; Basta, Ivana  ; Lavrnić, Dragana ; Stojanović, Vidosava Article
21M21
2015European founder haplotypes in Serbian patients with myotonic dystrophy type 2Kovčić Vlado; Perić, Stojan  ; Pešović, Jovan  ; Brkušanin, Miloš  ; Brajušković, Goran  ; Stanka Romac; Ranum Laura; Stojanović, Vidosava ; Savić-Pavićević, Dušanka  Conference Paper
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