Resultados de procura - Paul B. Augustijn

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  1. 1
    Shunting normal pressure hydrocephalus: the predictive value of combined clinical and CT data.

    Shunting normal pressure hydrocephalus: the predictive value of combined clinical and CT data. por J.A.L. Vanneste, Paul B. Augustijn, Wee Fu Tan, Clemens M.F. Dirven

    Publicado 1993
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  2. 2
    Nav1.1 dysfunction in genetic epilepsy with febrile seizures-plus or Dravet syndrome

    Nav1.1 dysfunction in genetic epilepsy with febrile seizures-plus or Dravet syndrome por Linda Volkers, Kristopher M. Kahlig, Nienke E. Verbeek, Joost H.G. Das, Marjan J. A. van Kempen, Hans Stroink, Paul B. Augustijn, Onno van Nieuwenhuizen, Dick Lindhout, Alfred L. George, Bobby P.C. Koeleman, Martin B. Rook

    Publicado 2011
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  3. 3
    Male patients affected by mosaic PCDH19 mutations: five new cases

    Male patients affected by mosaic PCDH19 mutations: five new cases por Iris Lange, Patrick Rump, Rinze F. Neuteboom, Paul B. Augustijn, K. Hodges, A. I. Kistemaker, Oebele F. Brouwer, Grazia M.S. Mancini, Hadas Newman, Yvonne J. Vos, Katherine L. Helbig, Cacha Peeters‐Scholte, Marjolein Kriek, N. Knoers, Dick Lindhout, Bobby P.C. Koeleman, Marjan J. A. van Kempen, Eva H. Brilstra

    Publicado 2017
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  4. 4
    Long-term neuropsychological outcome following pediatric anti-NMDAR encephalitis

    Long-term neuropsychological outcome following pediatric anti-NMDAR encephalitis por Marienke A.A.M. de Bruijn, Femke K. Aarsen, Marielle P. van Oosterhout, Marieke M van der Knoop, Coriene E. Catsman‐Berrevoets, Marco W.J. Schreurs, Anna E.M. Bastiaansen, Peter A.E. Sillevis Smitt, Rinze F. Neuteboom, Maarten J. Titulaer, Paul B. Augustijn, Dewi P. Bakker, Maartje Boon, Elisabeth A. Cats, Merijn Eikelenboom, Marc Engelen, C.P.W. Geleijns, Charlotte A. Haaxma, Joost Nicolai, J.M.F. Niermeijer, Erik H. Niks, E Peeters, R Portier, André B. Rietman, H.M. Schippers, Aad Verrips, Marie‐Claire Y. de Wit

    Publicado 2018
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  5. 5
    <i>GRIN2A</i>-related disorders: genotype and functional consequence predict phenotype

    <i>GRIN2A</i>-related disorders: genotype and functional consequence predict phenotype por Vincent Strehlow, Henrike Heyne, Danique R.M. Vlaskamp, Katie Marwick, Gabrielle Rudolf, Julitta de Bellescize, Saskia Biskup, Eva H. Brilstra, Oebele F. Brouwer, Petra M.C. Callenbach, Julia Hentschel, Édouard Hirsch, Peter C. Kind, Cyril Mignot, Konrad Platzer, P. Rump, Paul Skehel, David J. A. Wyllie, Giles E. Hardingham, Conny M.A. van Ravenswaaij‐Arts, Gaëtan Lesca, Johannes R. Lemke, Alexis Arzimanoglou, Paul B. Augustijn, Patrick Van Bogaert, Helene Bourry, Peter Burfeind, Yoyo W. Y. Chu, Brian Chung, Diane Doummar, Patrick Edery, Aviva Fattal‐Valevski, Mélanie Fradin, Marion Gérard, Christa de Geus, Boudewijn Gunning, Danielle Hasaerts, Ingo Helbig, Katherine L. Helbig, Rami Abou Jamra, Mélanie Jennesson Lyver, Jolien S. Klein Wassink‐Ruiter, David A. Koolen, Damien Lederer, Roelineke J. Lunsing, Mikaël Mathot, Hélène Maurey, Shay Menascu, Anne Michel, Ghayda Mirzaa, Diana Mitter, Hiltrud Muhle, Rikke S. Møller, Caroline Nava, Margaret O’Brien, Evelyn van Pinxteren-Nagler, Anne van Riesen, Christelle Rougeot, Damien Sanlaville, Jolanda Schieving, Steffen Syrbe, Hermine E. Veenstra‐Knol, Nienke E. Verbeek, Dorothée Ville, Yvonne J. Vos, Pascal Vrielynck, Sabrina Wagner, Sarah Weckhuysen, Marjolein H. Willemsen

    Publicado 2018
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