Joint effect of the SMN2 and SERF1A genes on childhood-onset types of spinal muscular atrophy in Serbian patients von Brkušanin, Miloš, Kosać, Ana, Jovanović, Vladimir, Pešović, Jovan, Brajušković, Goran, Dimitrijević, Nikola, Todorović, Slobodanka, Romac, Stanka, Milić Rašić, Vedrana, Savić-Pavićević, Dušanka

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MACF1 links Rapsyn to microtubule- and actin-binding proteins to maintain neuromuscular synapses von Oury, Julien, Liu, Yun, Töpf, Ana, Todorovic, Slobodanka, Hoedt, Esthelle, Preethish-Kumar, Veeramani, Neubert, Thomas A, Lin, Weichun, Lochmüller, Hanns, Burden, Steven J

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Proximal Dystrophin Gene Deletions and Protein Alterations in Becker Muscular Dystrophy von NOVAKOVIĆ, IVANA, BOJIĆ, DRAGANA, TODOROVIĆ, SLOBODANKA, APOSTOLSKI, SLOBODAN, LUKOVIĆ, LJILJANA, STEFANOVIĆ, DEJAN, MILAŠIN, JELENA

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MACF1 links Rapsyn to microtubule- and actin-binding proteins to maintain neuromuscular synapses von Oury, Julien, Liu, Yun, Töpf, Ana, Todorovic, Slobodanka, Hoedt, Esthelle, Preethish-Kumar, Veeramani, Neubert, Thomas A, Lin, Weichun, Lochmüller, Hanns, Burden, Steven J

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Loss-of-function mutations in HINT1 cause axonal neuropathy with neuromyotonia von 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, Savic-Pavicevic, Dusanka, Ishpekova, Boryana, Lechner, Silvia, Peeters, Kristien, Ooms, Tinne, Hahn, Angelika F, Züchner, Stephan, Timmerman, Vincent, Van Dijck, Patrick, Rasic, Vedrana Milic, Janecke, Andreas R, De Jonghe, Peter, Jordanova, Albena

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250 CTG repeats in DMPK is a threshold for correlation of expansion size and age at onset of juvenile-adult DM1 von Savić, Dušanka, Rakočvić-Stojanović, Vidosava, Keckarević, Dušan, Čuljković, Biljana, Stojković, Oliver, Mladenović, Jelena, Todorović, Slobodanka, Apostolski, Slobodan, Romac, Stanka

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Targeted Next-Generation Sequencing of a 12.5 Mb Homozygous Region Reveals ANO10 Mutations in Patients with Autosomal-Recessive Cerebellar Ataxia von 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, Milic-Rasic, 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

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CLINICAL CASE REPORT ATYPICAL MYOPATHY IN A YOUNG GIRL WITH 91 CTG REPEATS IN DM1 LOCUS AND A POSITIVE DM1 FAMILY HISTORY von SAVI, DUŠANKA, KECKAREVI, DUŠAN, BRANKOVI -SRE KOVI, VESNA, APOSTOLSKI, SLOBODAN, TODOROVI, SLOBODANKA, ROMAC, STANKA

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Eosinophilic myositis as presenting symptom in γ-sarcoglycanopathy von Baumeister, Sarah K, Todorovic, Slobodanka, Milić-Rašić, Vedrana, Dekomien, Gabriele, Lochmüller, Hanns, Walter, Maggie C

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Hypoxic-ischemic encefalopathy: Clinical course and prognosis von Cosic-Cerovac, Natasa, Todorovic, Slobodanka, Jovic, Nebojsa, Prostran, Milica

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Epidemiology of myotonic dystrophy type 1 (Steinert disease) in Belgrade (Serbia) von Mladenovic, Jelena, Pekmezovic, Tatjana, Todorovic, Slobodanka, Rakocevic-Stojanovic, Vidosava, Savic, Dusanka, Romac, Stanka, Apostolski, Slobodan

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Duchenne's/Becker's muscular dystrophy: Analysis of genotype-feno-type correlation in 28 patients von Keckarevic, Milica, Savic, Dusanka, Culjkovic, Biljana, Zamurovic, Natasa, Major, Tamara, Keckarevic, Dusan, Todorovic, Slobodanka, Romac, Stanka

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Epidemiology of myotonic dystrophy type 1 in the population of central Serbia von Mladenović, Jelena, Pekmezović, Tatjana, Todorović, Slobodanka, Rakocević-Stojanović, Vidosava, Romac, Stanka, Apostolski, Slobodan

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Atypical myopathy in a young girl with 91 CTG repeats in DM1 locus and a positive DM1 family history von SAVIC, Dusanka, KECKAREVIC, Dusan, BRANKOVIC-SRECKOVIC, Vesna, APOSTOLSKI, Slobodan, TODOROVIC, Slobodanka, ROMAC, Stanka

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P163 Electroneuromyography findings in patients with hereditary motor and sensory neuropathy type II von Nikodinović, Jelena, Milić-Rašić, Vedrana, Todorović, Slobodanka, Apostolski, Slobodan, Rakočević-Stojanović, Vidosava, Mladenović, Jelena, Dačković, Jelena

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Association of progressive myoclonic epilepsy and spinal muscular atrophy von Marjanovic, Borivoj, Todorovic, Slobodanka, Dozic, Slobodan

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Clinical course and prognosis in hypoxic-ischemic encephalopathy von Cerovac-Cosić, Natasa, Todorović, Slobodanka, Jović, Nebojsa, Prostran, Milica

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Is the 31 CAG repeat allele of the spinocerebellar ataxia 1 (SCA1) gene locus non-specifically associated with trinucleotide expansion diseases? von Savić, D, Topisirović, I, Keckarević, M, Keckarević, D, Major, T, Culjković, B, Stojković, O, Rakocević-Stojanović, V, Mladenović, J, Todorović, S, Apostolski, S, Romac, S

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Duchenne's and Becker's muscular dystrophy: analysis of phenotype-genotype correlation in 28 patients von Keckarević, Milica, Savić, Dusanka, Culjković, Biljana, Zamurović, Natasa, Major, Tamara, Keckarević, Dusan, Todorović, Slobodanka, Romac, Stanka

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Association of Krabbe leukodystrophy and congenital fiber type disproportion von Marjanovic, Borivoj, Cvetković, Dubravka, Dozić, Slobodan, Todorović, Slobodanka, Djurić, Milena

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