Pediatric stroke related to Lyme neuroborreliosis: Data from the Swiss NeuroPaediatric Stroke Registry and literature review von Monteventi, O., Steinlin, M., Regényi, M., Roulet-Perez, E., Weber, P., Fluss, J.

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Visuospatial working memory in very preterm and term born children—Impact of age and performance von Mürner-Lavanchy, I., Ritter, B.C., Spencer-Smith, M.M., Perrig, W.J., Schroth, G., Steinlin, M., Everts, R.

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Neuropsychological long‐term sequelae after posterior fossa tumour resection during childhood von Steinlin, Maja, Imfeld, Sara, Zulauf, Prisca, Boltshauser, Eugen, Lövblad, Karl‐Olaf, Lüthy, Annette Ridolfi, Perrig, Walter, Kaufmann, Franz

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Prediction of ROP Treatment and Evaluation of Screening Criteria in VLBW Infants–a Population Based Analysis von Gerull, Roland, Brauer, Viviane, Bassler, Dirk, Laubscher, Bernard, Pfister, Riccardo E, Nelle, Mathias, Müller, Beatrice, Roth-Kleiner, Matthias, Gerth-Kahlert, Christina, Adams, Mark

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Childhood stroke : What are the special features of childhood stroke? von Gerstl, L, Bonfert, M V, Nicolai, T, Dieterich, M, Adamczyk, C, Heinen, F, Olivieri, M, Steinlin, M

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Acute transverse myelitis in Lyme neuroborreliosis von Bigi, S, Aebi, C, Nauer, C, Bigler, S, Steinlin, M

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Muscle pain and mild proximal weakness can be due to vitamin D deficiency von Perret Hoigné, E, Zaugg, Ch, Capone Mori, A, Martin, F, Knirsch, U, Relly, Ch, Steinlin, M, Klein, A

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The First Three Years of the Swiss Neuropaediatric Stroke Registry (SNPSR): A Population-Based Study of Incidence, Symptoms and Risk Factors von Steinlin, M., Pfister, I., Pavlovic, J., Everts, R., Boltshauser, E., Capone Mori, A., Gubser Mercati, D., Hänggeli, C.-A., Keller, E., Luetschg, J., Marcoz, J., Ramelli, G.-P., Roulet Perez, E., Schmitt-Mechelke, T., Weissert, M.

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INV9 Prognosis of stroke in childhood von Steinlin, M

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P11. Quality of Life after pediatric ischemic stroke: Five year follow-up of swiss children von Kornfeld, S, Winkelbeiner, S, Studer, M, Boltshauser, E, Capone Mori, A, Datta, A, Fluss, J, Mercati, D, Hackenberg, A, Keller, E, Maier, O, Marcoz, J.P, Ramelli, G.P, Poloni, C, Schmid, R, Schmitt-Mechelke, T, Wehrli, E, Heinks, T, Steinlin, M

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Cavernous malformations of the central nervous system in children: Presentation, treatment and outcome of 20 cases von Bigi, S, Capone Mori, A, Steinlin, M, Remonda, L, Landolt, H, Boltshauser, E

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Effects of Cognitive Training and Exergaming in Pediatric Cancer Survivors—A Randomized Clinical Trial von BENZING, VALENTIN, SPITZHÜTTL, JANINE, SIEGWART, VALERIE, SCHMID, JÜRG, GROTZER, MICHAEL, HEINKS, THEDA, ROEBERS, CLAUDIA M., STEINLIN, MAJA, LEIBUNDGUT, KURT, SCHMIDT, MIRKO, EVERTS, REGULA

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Neuropsychological Problems after Paediatric Stroke: Two Year Follow-Up of Swiss Children von Pavlovic, J., Kaufmann, F., Boltshauser, E., Capone Mori, A., Gubser Mercati, D., Haenggeli, C.-A., Keller, E., Lütschg, J., Marcoz, J.-P., Ramelli, G.-P., Roulet Perez, E., Schmitt-Mechelke, T., Weissert, M., Steinlin, M.

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Impact of sepsis on neurodevelopmental outcome in a Swiss National Cohort of extremely premature infants von Schlapbach, Luregn J, Aebischer, Maude, Adams, Mark, Natalucci, Giancarlo, Bonhoeffer, Jan, Latzin, Philipp, Nelle, Mathias, Bucher, Hans Ulrich, Latal, Beatrice

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Follow-Up in Children with Joubert Syndrome von Steinlin, M., Schmid, M., Landau, K., Boltshauser, E.

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Contiguous ~16Mb 1p36 deletion: Dominant features of classical distal 1p36 monosomy with haplo-lethality von Nicoulaz, A, Rubi, F, Lieder, L, Wolf, R, Goeggel-Simonetti, B, Steinlin, M, Wiest, R, Bonel, H M, Schaller, A, Gallati, S, Conrad, B

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Loss of tubulin deglutamylase CCP1 causes infantile‐onset neurodegeneration von Shashi, Vandana, Magiera, Maria M, Klein, Dennis, Zaki, Maha, Schoch, Kelly, Rudnik‐Schöneborn, Sabine, Norman, Andrew, Lopes Abath Neto, Osorio, Dusl, Marina, Yuan, Xidi, Bartesaghi, Luca, De Marco, Patrizia, Alfares, Ahmed A, Marom, Ronit, Arold, Stefan T, Guzmán‐Vega, Francisco J, Pena, Loren DM, Smith, Edward C, Steinlin, Maja, Babiker, Mohamed OE, Mohassel, Payam, Foley, A Reghan, Donkervoort, Sandra, Kaur, Rupleen, Ghosh, Partha S, Stanley, Valentina, Musaev, Damir, Nava, Caroline, Mignot, Cyril, Keren, Boris, Scala, Marcello, Tassano, Elisa, Picco, Paolo, Doneda, Paola, Fiorillo, Chiara, Issa, Mahmoud Y, Alassiri, Ali, Alahmad, Ahmed, Gerard, Amanda, Liu, Pengfei, Yang, Yaping, Ertl‐Wagner, Birgit, Kranz, Peter G, Wentzensen, Ingrid M, Stucka, Rolf, Stong, Nicholas, Allen, Andrew S, Goldstein, David B, Schoser, Benedikt, Rösler, Kai M, Alfadhel, Majid, Capra, Valeria, Chrast, Roman, Strom, Tim M, Kamsteeg, Erik‐Jan, Bönnemann, Carsten G, Gleeson, Joseph G, Martini, Rudolf, Janke, Carsten, Senderek, Jan

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Progressive myelopathy in a case of suspected Proteus syndrome von Strasser, M, Steinlin, M

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Predicting the outcome of postasphyxial hypoxic-ischemic encephalopathy within 4 hours of birth von EKERT, P, PERLMAN, M, STEINLIN, M, HAO, Y

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Pontocerebellar hypoplasia type 1: Clinical spectrum and relevance of EXOSC3 mutations von RUDNIK-SCHÖNEBORN, Sabine, SENDEREK, Jan, SEEGER, Jürgen, RYAN, Monique M, MUNTONI, Francesco, STEINLIN, Maja, SZTRIHA, Laszlo, COLOMER, Jaume, HÜBNER, Christoph, BROCKMANN, Knut, VAN MALDERGEM, Lionel, SCHIFF, Manuel, JEN, Joanna C, HOLZINGER, Andreas, BARTH, Peter, REARDON, William, YOURSHAW, Michael, NELSON, Stanley F, EGGERMANN, Thomas, ZERRES, Klaus, HOUGE, Gunnar, SEEMAN, Pavel, PUCHMAJEROVA, Alena, GRAUL-NEUMANN, Luitgard, SEIDEL, Ulrich, KORINTHENBERG, Rudolf, KIRSCHNER, Janbernd

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