Nine patients with a microdeletion 15q11.2 between breakpoints 1 and 2 of the Prader–Willi critical region, possibly associated with behavioural disturbances by Doornbos, Marianne, Sikkema-Raddatz, Birgit, Ruijvenkamp, Claudia A.L, Dijkhuizen, Trijnie, Bijlsma, Emilia K, Gijsbers, Antoinet C.J, Hilhorst-Hofstee, Yvonne, Hordijk, Roel, Verbruggen, Krijn T, Kerstjens-Frederikse, W.S. (Mieke), van Essen, Ton, Kok, Klaas, van Silfhout, Anneke T, Breuning, Martijn, van Ravenswaaij-Arts, Conny M.A

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International Guillain‐Barré Syndrome Outcome Study: protocol of a prospective observational cohort study on clinical and biological predictors of disease course and outcome in Gui... by Jacobs, Bart C., van den Berg, Bianca, Cornblath, David R., Harbo, Thomas, van Doorn, Pieter A., Jacobs, B.C., Gorson, K.C., Hartung, H.P., Willison, H.J., van den Berg, B., Roodbol, J., Reddel, S.W., Islam, Z., Islam, B., Mohammad, Q.D., van den Bergh, P., Feasby, T.E., Wang, Y.Z., Hartung, H.P., Lehmann, H.C., Nobile‐Orazio, E., Shahrizaila, N., Jacobs, B.C., Verboon, C., Bateman, K., Chavada, G., Davidson, A., Ajroud‐Driss, S., Andersen, H., Antonini, G., Barroso, F.A., Beronio, A., Bianco, M., Bürmann, J., Bhavaraju‐Sanka, R., Brannagan, T.H., Campagnolo, M., Casasnovas, C., Cavaletti, G., Chen, S., Chetty, S., Cohen, J.A., Conti, M.E., Dalakas, M.C., Dimachkie, M.M., Domínguez González, C., Doppler, K., Dornonville de la Cour, C., Eftimov, F., Faber, C.G., Galassi, G., Garcia, T., Garnero, M., Gijsbers, C.J., Gilchrist, J.M., Gutiérrez Gutiérrez, G., Hadden, R.D.M., Holbech, J.V., Kaida, K., Kokubun, N., Kolb, N.A., Ledingham, D., Léon Cejas, L., Luciano, C.A., Lunn, M.P.T., Marfia, G.A.M., Márquez Infante, C., Martinez Hernandez, E., Miller, J., Monges, M.S., Montero, M.C.J., Neumann, C., Nowak, R.J., Pardo Fernandez, J., Pasnoor, M., Pulley, M.T., Rudnicki, S.A., Samijn, J.P.A., Santoro, L., Sedano Tous, M.J., Sekiguchi, Y., Sindrup, S.H., Stein, B., Stino, A.M., Spyropoulos, A., Srinivasan, J., Suzuki, H., Tankisi, H., Valzania, F., van der Ree, T., van Koningsveld, R., Varrato, J.D., Vermeij, F.H., Visser, L.H., Vytopil, M.V., Wilkerson, C., Wirtz, P.W., Yamagishi, Y., Zhou, L., Zivkovic, S.

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Second IVIg course in Guillain‐Barré syndrome patients with poor prognosis (SID‐GBS trial): Protocol for a double‐blind randomized, placebo‐controlled clinical trial by Walgaard, Christa, Jacobs, Bart C., Lingsma, Hester F., Steyerberg, Ewout W., Cornblath, David R., van Doorn, Pieter A., van Doorn, P.A., Jacobs, B.C., Walgaard, C., de Wit, M.C.Y., Steyerberg, E.W., Cornblath, D.R., van den Berg, B., Doets, A.Y., van Doorn, P.A., Jacobs, B.C., Leonhard, S.E., Verboon, J.C., Walgaard, C., van Woerkom, M., Tio‐Gillen, A.P., van Rijs, W., Huizinga, H., Badrising, U.A., Bienfait, H.M.E., Blom, R.J., van Boheemen, C.J.M., Breukelman, A.J., Bronner, I.M., Dieks, H.J.G., van Dijk, G.W., van Engelen, B.G.M., Faber, C.G., Feenstra, B., Fokke, C., Garssen, M.P.J., Gijsbers, C.J., Gilhuis, H. J., van der Graaff, M.M., Groen, R.J., Hoogendoorn, T.A., Hovestad, A., Jansen, P.J.H.W., Jellema, K., Keuter, E., Kleyweg, R.P., van Koningsveld, R., van der Kooi, A.J., van der Kooi, E.L., Krudde, J., Kuks, J.B.M., Kuitwaard, K., Linssen, W.H.J.P., Lion, J., Lovenich, H., Manschot, S.M., Mellema, S.J., Merkies, I.S.J., van der Meulen, M.F.G., van der Meulen, W.D.M., Molenaar, D.S.M., Oenema, D.G., van Oosten, B.W., van Oostrom, J.C.H., van Orshoven, N.P., van der Ploeg, R.J.O, van der Pol, W.L., Polman, S., van der Ree, T.C., de Rijk, M.C., Ruitenberg, A., Ruts, L., Samijn, J.P.A., Schyns‐Soeterboek, A.J.G.M., Stevens, M., Vermeij, F.H., Verschuuren, J.J.G.M., Visser, L.H., Wirtz, P.W., Wohlgemuth, M., Zwetsloot, C.P., Lingsma, H.F., Steyerberg, E.W., Dippel, D.W.J., Hintzen, R.Q.

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Molecular and clinical characterization of patients with a ring chromosome 11 by Hansson, Kerstin B.M, Gijsbers, Antoinet C.J, Oostdijk, Wilma, Rehbock, Jan J.B, de Snoo, Femke, Ruivenkamp, Claudia A.L, Kant, Sarina G

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Additional cryptic CNVs in mentally retarded patients with apparently balanced karyotypes by Gijsbers, Antoinet C.J, Bosch, Cathy A.J, Dauwerse, Johannes G, Giromus, Osdilly, Hansson, Kerstin, Hilhorst-Hofstee, Yvonne, Kriek, Marjolein, van Haeringen, Arie, Bijlsma, Emilia K, Bakker, Egbert, Breuning, Martijn H, Ruivenkamp, Claudia A.L

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Three new cases with a mosaicism involving a normal cell line and a cryptic unbalanced autosomal reciprocal translocation by Gijsbers, Antoinet C.J, Dauwerse, Johannes G, Bosch, Cathy A.J, Boon, Elles M.J, van den Ende, Wilco, Kant, Sarina G, Hansson, Kerstin M.B, Breuning, Martijn H, Bakker, Egbert, Ruivenkamp, Claudia A.L

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A 797 kb de novo deletion of 18q21.31 in a patient with speech delay, mental retardation, sleeping problems, facial dysmorphism, and feet anomalies by van Diepen, Mireille M.L, Gijsbers, Antoinet C.J, Bosch, Cathy A.J, Oudesluys-Murphy, Anne Marie, Ruivenkamp, Claudia A.L, Bijlsma, Emilia K

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A 400 kb duplication, 2.4 Mb triplication and 130 kb duplication of 9q34.3 in a patient with severe mental retardation by Gijsbers, Antoinet C.J, Bijlsma, Emilia K, Weiss, Marjan M, Bakker, Egbert, Breuning, Martijn H, Hoffer, Mariëtte J.V, Ruivenkamp, Claudia A.L

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X-chromosome duplications in males with mental retardation: pathogenic or benign variants? by Gijsbers, ACJ, Den Hollander, NS, Helderman-van de Enden, ATJM, Schuurs-Hoeijmakers, JHM, Vijfhuizen, L, Bijlsma, EK, Van Haeringen, A, Hansson, KBM, Bakker, E, Breuning, MH, Ruivenkamp, CAL

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A 400kb duplication, 2.4Mb triplication and 130kbduplication of 9q34.3 in a patient with severe mental retardation by Gijsbers, Antoinet C.J., Bijlsma, Emilia K., Weiss, Marjan M., Bakker, Egbert, Breuning, Martijn H., Hoffer, Mariëtte J.V., Ruivenkamp, Claudia A.L.

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