Levetiracetam Monotherapy in Children with Epilepsy: A Systematic Review

por Weijenberg, Amerins, Brouwer, Oebele F., Callenbach, Petra M. C.
Publicado 2015

Investigator‐initiated randomized controlled trials in children with epilepsy: Mission impossible?

por Weijenberg, Amerins, Callenbach, Petra M. C., Brouwer, Oebele F.
Publicado 2016

Acute flaccid myelitis and Guillain–Barré syndrome in children: A comparative study with evaluation of diagnostic criteria

por Helfferich, Jelte, Roodbol, Joyce, de Wit, Marie‐Claire, Brouwer, Oebele F., Jacobs, Bart C.
Publicado 2021

Histological characterisation of segmental neuromuscular dysfunction in fetuses with spina bifida aperta

por Sival, Deborah A, Brouwer, Oebele F, Verbeek, Renate J, Sollie, Krystyna M, den Dunnen, Wilfred F
Publicado 2006

Fetal operation followed by Caesarean section may have a beneficial effect upon neuromuscular function in spina bifida aperta

por Verbeek, Renate, Heep, Axel, Maurits, Natasha, Cremer, Reinhold, Brouwer, Oebele, Hoeven, Johannes van der, Sival, Deborah
Publicado 2009

Does fetal endoscopic closure of the myelomeningocele prevent loss of neurologic function in spina bifida aperta?

por Verbeek, Renate, Heep, Axel, Maurits, Natasha, Cremer, Reinhold, Brouwer, Oebele, van der Hoeven, Johannes, Sival, Deborah
Publicado 2010

Ketogenic Diet in Refractory Childhood Epilepsy: Starting With a Liquid Formulation in an Outpatient Setting

por Weijenberg, Amerins, van Rijn, Margreet, Callenbach, Petra M. C., de Koning, Tom J., Brouwer, Oebele F.
Publicado 2018

Twenty-nine Cases of Enterovirus-D68–associated Acute Flaccid Myelitis in Europe 2016: A Case Series and Epidemiologic Overview

por Knoester, Marjolein, Helfferich, Jelte, Poelman, Randy, Van Leer-Buter, Coretta, Brouwer, Oebele F., Niesters, Hubert G. M.
Publicado 2019

Acute flaccid myelitis and enterovirus D68: lessons from the past and present

por Helfferich, Jelte, Knoester, Marjolein, Van Leer-Buter, Coretta C., Neuteboom, Rinze F., Meiners, Linda C., Niesters, Hubert G., Brouwer, Oebele F.
Publicado 2019

Unusual Course of Lafora Disease

por Zutt, Rodi, Drost, Gea, Vos, Yvonne J., Elting, Jan Willem, Miedema, Irene, Tijssen, Marina A. J., Brouwer, Oebele F., de Jong, Bauke M.
Publicado 2016

Copy number variation in a hospital‐based cohort of children with epilepsy

por Vlaskamp, Danique R. M., Callenbach, Petra M. C., Rump, Patrick, Giannini, Lucia A. A., Dijkhuizen, Trijnie, Brouwer, Oebele F., van Ravenswaaij‐Arts, Conny M. A.
Publicado 2017

Pathogenesis of cerebral malformations in human fetuses with meningomyelocele

por de Wit, Olga A, den Dunnen, Wilfred FA, Sollie, Krystyne M, Muñoz, Rosa Iris, Meiners, Linda C, Brouwer, Oebele F, Rodríguez, Esteban M, Sival, Deborah A
Publicado 2008

Neuronal antibodies in pediatric epilepsy: Clinical features and long‐term outcomes of a historical cohort not treated with immunotherapy

por Wright, Sukhvir, Geerts, Ada T., Jol‐van der Zijde, Cornelia Maria, Jacobson, Leslie, Lang, Bethan, Waters, Patrick, van Tol, Maarten J. D., Stroink, Hans, Neuteboom, Rinze F., Brouwer, Oebele F., Vincent, Angela
Publicado 2016

The efficacy of the modified Atkins diet in North Sea Progressive Myoclonus Epilepsy: an observational prospective open-label study

por van Egmond, Martje E., Weijenberg, Amerins, van Rijn, Margreet E., Elting, Jan Willem J., Gelauff, Jeannette M., Zutt, Rodi, Sival, Deborah A., Lambrechts, Roald A., Tijssen, Marina A. J., Brouwer, Oebele F., de Koning, Tom J.
Publicado 2017

Genome wide high density SNP-based linkage analysis of childhood absence epilepsy identifies a susceptibility locus on chromosome 3p23-p14

por Chioza, Barry A., Aicardi, Jean, Aschauer, Harald, Brouwer, Oebele, Callenbach, Petra, Covanis, Athanasios, Dooley, Joseph M., Dulac, Olivier, Durner, Martina, Eeg-Olofsson, Orvar, Feucht, Martha, Friis, Mogens Laue, Guerrini, Renzo, Kjeldsen, Marianne Juel, Nabbout, Rima, Nashef, Lina, Sander, Thomas, Sirén, Auli, Wirrell, Elaine, McKeigue, Paul, Robinson, Robert, Gardiner, R. Mark, Everett, Kate V.
Publicado 2009

Epidemiology of acute flaccid myelitis in children in the Netherlands, 2014 to 2019

por Helfferich, Jelte, de Lange, Marit MA, Benschop, Kimberley SM, Jacobs, Bart C, Van Leer-Buter, Coretta C, Meijer, Adam, Bakker, Dewi P, de Bie, Eva, Braakman, Hilde MH, Brandsma, Rick, Neuteboom, Rinze F, Niks, Erik H, Niermeijer, Jikke-Mien, Roelfsema, Vincent, Schoenmaker, Niels, Sie, Lilian T, Niesters, Hubert G, Brouwer, Oebele F, te Wierik, Margreet JM
Publicado 2022

GRIN2A-related disorders: genotype and functional consequence predict phenotype

por Strehlow, Vincent, Heyne, Henrike O, Vlaskamp, Danique R M, Marwick, Katie F M, Rudolf, Gabrielle, de Bellescize, Julitta, Biskup, Saskia, Brilstra, Eva H, Brouwer, Oebele F, Callenbach, Petra M C, Hentschel, Julia, Hirsch, Edouard, Kind, Peter C, Mignot, Cyril, Platzer, Konrad, Rump, Patrick, Skehel, Paul A, Wyllie, David J A, Hardingham, Giles E, van Ravenswaaij-Arts, Conny M A, Lesca, Gaetan, Lemke, Johannes R
Publicado 2019