Xanthine oxidase activity in patients with age-related cataract associated with hypertension von Kisic, B, Miric, D, Zoric, L, Rasic, J V, Grbic, R, Popovic, Lj M, Arsic, A M

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Mutations in SACS cause atypical and late-onset forms of ARSACS von BAETS, J, DECONINCK, T, ROBBERECHT, W, DE MEIRLEIR, L, MICHIELSENS, B, DEL-FAVERO, J, JORDANOVA, A, DE JONGHE, P, SMETS, K, GOOSSENS, D, VAN DEN BERGH, P, DAHAN, K, SCHMEDDING, E, SANTENS, P, MILIC RASIC, V, VAN DAMME, P

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MFN2 mutation distribution and genotype/phenotype correlation in Charcot–Marie–Tooth type 2 von Verhoeven, Kristien, Claeys, Kristl G., Züchner, Stephan, Schröder, J. Michael, Weis, Joachim, Ceuterick, Chantal, Jordanova, Albena, Nelis, Eva, De Vriendt, Els, Van Hul, Matthias, Seeman, Pavel, Mazanec, Radim, Saifi, Gulam Mustafa, Szigeti, Kinga, Mancias, Pedro, Butler, Ian J., Kochanski, Andrzej, Ryniewicz, Barbara, De Bleecker, Jan, Van den Bergh, Peter, Verellen, Christine, Van Coster, Rudy, Goemans, Nathalie, Auer-Grumbach, Michaela, Robberecht, Wim, Milic Rasic, Vedrana, Nevo, Yoram, Tournev, Ivajlo, Guergueltcheva, Velina, Roelens, Filip, Vieregge, Peter, Vinci, Paolo, Moreno, Maria Teresa, Christen, H.-J., Shy, Michael E., Lupski, James R., Vance, Jeffery M., De Jonghe, Peter, Timmerman, Vincent

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Relative contribution of mutations in genes for autosomal dominant distal hereditary motor neuropathies: a genotype–phenotype correlation study von 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

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Influence of Higenamine on Exercise Performance of Recreational Female Athletes: A Randomized Double-Blinded Placebo-Controlled Trial von Rasic, Jelena S., Ivanovic, Nevena D. J., Andjelkovic, Marija S., Nedeljkovic, Ivana P., Nikolic, Ivan R., Stojanovic, Sava D., Ristic-Medic, Danijela K., Takic, Marija M., Djordjevic, Brizita, Dikic, Nenad

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Improved reference genome of Aedes aegypti informs arbovirus vector control von Matthews, Benjamin J., Dudchenko, Olga, Kingan, Sarah B., Koren, Sergey, Antoshechkin, Igor, Crawford, Jacob E., Glassford, William J., Herre, Margaret, Redmond, Seth N., Rose, Noah H., Weedall, Gareth D., Wu, Yang, Batra, Sanjit S., Brito-Sierra, Carlos A., Buckingham, Steven D., Campbell, Corey L., Chan, Saki, Cox, Eric, Evans, Benjamin R., Fansiri, Thanyalak, Filipović, Igor, Fontaine, Albin, Gloria-Soria, Andrea, Hall, Richard, Joardar, Vinita S., Jones, Andrew K., Kay, Raissa G. G., Kodali, Vamsi K., Lee, Joyce, Lycett, Gareth J., Mitchell, Sara N., Muehling, Jill, Murphy, Michael R., Omer, Arina D., Partridge, Frederick A., Peluso, Paul, Aiden, Aviva Presser, Ramasamy, Vidya, Rašić, Gordana, Roy, Sourav, Saavedra-Rodriguez, Karla, Sharan, Shruti, Sharma, Atashi, Smith, Melissa Laird, Turner, Joe, Weakley, Allison M., Zhao, Zhilei, Akbari, Omar S., Black, William C., Cao, Han, Darby, Alistair C., Hill, Catherine A., Johnston, J. Spencer, Murphy, Terence D., Raikhel, Alexander S., Sattelle, David B., Sharakhov, Igor V., White, Bradley J., Zhao, Li, Aiden, Erez Lieberman, Mann, Richard S., Lambrechts, Louis, Powell, Jeffrey R., Sharakhova, Maria V., Tu, Zhijian, Robertson, Hugh M., McBride, Carolyn S., Hastie, Alex R., Korlach, Jonas, Neafsey, Daniel E., Phillippy, Adam M., Vosshall, Leslie B.

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Intellectual Ability in the Duchenne Muscular Dystrophy and Dystrophin Gene Mutation Location von Rasic, Milic V., Vojinovic, D., Pesovic, J., Mijalkovic, G., Lukic, V., Mladenovic, J., Kosac, A., Novakovic, I., Maksimovic, N., Romac, S., Todorovic, S., Pavicevic, Savic D.

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A Multi-Stain Breast Cancer Histological Whole-Slide-Image Data Set from Routine Diagnostics von Weitz, Philippe, Valkonen, Masi, Solorzano, Leslie, Carr, Circe, Kartasalo, Kimmo, Boissin, Constance, Koivukoski, Sonja, Kuusela, Aino, Rasic, Dusan, Feng, Yanbo, Sinius Pouplier, Sandra, Sharma, Abhinav, Ledesma Eriksson, Kajsa, Latonen, Leena, Laenkholm, Anne-Vibeke, Hartman, Johan, Ruusuvuori, Pekka, Rantalainen, Mattias

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156P Phosphorylated neurofilament heavy chain in cerebrospinal fluid and plasma in clinically silent and childhood-onset SMA individuals from Serbia von Brkusanin, M., Kosac, A., Brankovic-Sreckovic, V., Jovanovic, K., Karanovic, J., Matijasevic Jokovic, S., Garai, N., Pesovic, J., Radovanovic, N., Radenkovic, L., Dobrijevic, Z., Nikolic, D., Stevic, Z., Brajuskovic, G., Milic-Rasic, V., Savic-Pavicevic, D.

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Structural investigation of mechanically activated ZnO powder von Peles, A, Pavlovic, V P, Filipovic, S, Obradovic, N, Mancic, L, Krstic, J, Mitric, M, Vlahovic, B, Rasic, G, Kosanovic, D, Pavlovic, V B

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Epidemiology of Charcot-Marie-Tooth Disease in the Population of Belgrade, Serbia von Mladenovic, J., Milic Rasic, V., Keckarevic Markovic, M., Romac, S., Todorovic, S., Rakocevic Stojanovic, V., Kisic Tepavcevic, D., Hofman, A., Pekmezovic, T.

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Exercise Decreases Susceptibility to Homocysteine Seizures: the Role of Oxidative Stress von Hrncic, D., Rasic-Markovic, A., Lekovic, J., Krstic, D., Colovic, M., Macut, D., Susic, V., Djuric, D., Stanojlovic, O.

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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 von 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

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4.Electromyography test as diagnostic procedure in recessive cerebellar ataxias von Milic Rasic, V, Todorovic, S, Brankovic, V, Novakovic, I, Baets, J, Vermeer, S

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Impaired receptor clustering in congenital myasthenic syndrome with novel RAPSN mutations von MÜLLER, J. S, BAUMEISTER, S. K, RASIC, V. M, KRAUSE, S, TODOROVIC, S, KUGLER, K, MÜLLER-FELBER, W, ABICHT, A, LOCHMÜLLER, H

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19. Multimodal evoked potentials in hereditary motor and sensory neuropathy type 1 von Jancic, J, Milic-Rasic, V, Mladenovic, J

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4. Neurophysiologic and clinical characteristic of neuromyotonia in new hereditary neuromuscular disorder von Milic Rasic, V, Nikodinovic, J, Mladenovic, J, De Jonghe, P, Jordanova, A, Baets, J, Zimon, M, Keckarevic Markovic, M, Savic Pavicevic, D, Todorovic, S

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N88S mutation in the BSCL2 gene in a Serbian family with distal hereditary motor neuropathy type V or Silver syndrome von Rakočević-Stojanović, V, Milić-Rašić, V, Perić, S, Baets, J, Timmerman, V, Dierick, I, Pavlović, S, De Jonghe, P

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Roadmap on biological pathways for electronic nanofabrication and materials von Bathe, Mark, Chrisey, Linda A, Herr, Daniel J C, Lin, Qinghuang, Rasic, Daniel, Woolley, Adam T, Zadegan, Reza M., Zhirnov, Victor V

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PP12.16 – 2973: Congenital cerebellar ataxias – Clinical, radiological and genetic considerations von Brankovic, V, Zekavica, A, Popara, J, Rasic, V. Milic

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