Impaired receptor clustering in congenital myasthenic syndrome with novel RAPSN mutations
Müller, J S, Baumeister, S K, Rasic, V M, Krause, S, Todorovic, S, Kugler, K, Müller-Felber, W, Abicht, A, Lochmüller, H
Published in Neurology (10.10.2006)
Published in Neurology (10.10.2006)
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Mutations in SACS cause atypical and late-onset forms of ARSACS
Baets, J, Deconinck, T, Smets, K, Goossens, D, Van den Bergh, P, Dahan, K, Schmedding, E, Santens, P, Rasic, V Milic, Van Damme, P, Robberecht, W, De Meirleir, L, Michielsens, B, Del-Favero, J, Jordanova, A, De Jonghe, P
Published in Neurology (28.09.2010)
Published in Neurology (28.09.2010)
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Relative contribution of mutations in genes for autosomal dominant distal hereditary motor neuropathies: a genotype–phenotype correlation study
Dierick, Ines, Baets, Jonathan, Irobi, Joy, Jacobs, An, De Vriendt, Els, Deconinck, Tine, Merlini, Luciano, Van den Bergh, Peter, Rasic, Vedrana Milic, Robberecht, Wim, Fischer, Dirk, Morales, Raul Juntas, Mitrovic, Zoran, Seeman, Pavel, Mazanec, Radim, Kochanski, Andrzej, Jordanova, Albena, Auer-Grumbach, Michaela, Helderman-van den Enden, A. T. J. M., Wokke, John H. J., Nelis, Eva, De Jonghe, Peter, Timmerman, Vincent
Published in Brain (London, England : 1878) (01.05.2008)
Published in Brain (London, England : 1878) (01.05.2008)
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Mapping the differences in care for 5,000 Spinal Muscular Atrophy patients, a survey of 24 national registries in North America, Australasia and Europe
Bladen, Catherine L., Thompson, Rachel, Jackson, Jacqueline M., Garland, Connie, Wegel, Claire, Ambrosini, Anna, Pisano, Paolo, Walter, Maggie C., Schreiber, Olivia, Lusakowska, Anna, Jedrzejowska, Maria, Kostera-Pruszczyk, Anna, van der Pol, Ludo, Wadman, Renske I., Gredal, Ole, Karaduman, Ayse, Topaloglu, Haluk, Yilmaz, Oznur, Matyushenko, Vitaliy, Rasic, Vedrana Milic, Kosac, Ana, Karcagi, Veronika, Garami, Marta, Herczegfalvi, Agnes, Monges, Soledad, Moresco, Angelica, Chertkoff, Lilien, Chamova, Teodora, Guergueltcheva, Velina, Butoianu, Niculina, Craiu, Dana, Korngut, Lawrence, Campbell, Craig, Haberlova, Jana, Strenkova, Jana, Alejandro, Moises, Jimenez, Alatorre, Ortiz, Genaro Gabriel, Enriquez, Gracia Viviana Gonzalez, Rodrigues, Miriam, Roxburgh, Richard, Dawkins, Hugh, Youngs, Leanne, Lahdetie, Jaana, Angelkova, Natalija, Saugier-Veber, Pascal, Cuisset, Jean-Marie, Bloetzer, Clemens, Jeannet, Pierre-Yves, Klein, Andrea, Nascimento, Andres, Tizzano, Eduardo, Salgado, David, Mercuri, Eugenio, Sejersen, Thomas, Kirschner, Jan, Rafferty, Karen, Straub, Volker, Bushby, Kate, Verschuuren, Jan, Beroud, Christophe, Lochmüller, Hanns
Published in Journal of neurology (2014)
Published in Journal of neurology (2014)
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INHERITED THROMBOPHILIA AS A RISK FACTOR FOR STROKE IN SERBIAN CHILDREN
Brankovic-Sreckovic, V, Rasic, VM, Djordjevic, V, Rakicevic, L
Published in Neuropediatrics (18.05.2006)
Published in Neuropediatrics (18.05.2006)
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