Mutations in DEPDC5 cause familial focal epilepsy with variable foci
Dibbens, Leanne M, de Vries, Boukje, Donatello, Simona, Heron, Sarah E, Hodgson, Bree L, Chintawar, Satyan, Crompton, Douglas E, Hughes, James N, Bellows, Susannah T, Klein, Karl Martin, Callenbach, Petra M C, Corbett, Mark A, Gardner, Alison E, Kivity, Sara, Iona, Xenia, Regan, Brigid M, Weller, Claudia M, Crimmins, Denis, O'Brien, Terence J, Guerrero-López, Rosa, Mulley, John C, Dubeau, Francois, Licchetta, Laura, Bisulli, Francesca, Cossette, Patrick, Thomas, Paul Q, Gecz, Jozef, Serratosa, Jose, Brouwer, Oebele F, Andermann, Frederick, Andermann, Eva, van den Maagdenberg, Arn M J M, Pandolfo, Massimo, Berkovic, Samuel F, Scheffer, Ingrid E
Published in Nature genetics (01.05.2013)
Published in Nature genetics (01.05.2013)
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Cohesin complex-associated holoprosencephaly
Kruszka, Paul, Berger, Seth I, Casa, Valentina, Dekker, Mike R, Gaesser, Jenna, Weiss, Karin, Martinez, Ariel F, Murdock, David R, Louie, Raymond J, Prijoles, Eloise J, Lichty, Angie W, Brouwer, Oebele F, Zonneveld-Huijssoon, Evelien, Stephan, Mark J, Hogue, Jacob, Hu, Ping, Tanima-Nagai, Momoko, Everson, Joshua L, Prasad, Chitra, Cereda, Anna, Iascone, Maria, Schreiber, Allison, Zurcher, Vickie, Corsten-Janssen, Nicole, Escobar, Luis, Clegg, Nancy J, Delgado, Mauricio R, Hajirnis, Omkar, Balasubramanian, Meena, Kayserili, Hülya, Deardorff, Matthew, Poot, Raymond A, Wendt, Kerstin S, Lipinski, Robert J, Muenke, Maximilian
Published in Brain (London, England : 1878) (01.09.2019)
Published in Brain (London, England : 1878) (01.09.2019)
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Fetal endoscopic myelomeningocele closure preserves segmental neurological function
VERBEEK, RENATE J, HEEP, AXEL, MAURITS, NATALIA M, CREMER, REINHOLD, HOVING, EELCO W, BROUWER, OEBELE F, VAN DER HOEVEN, JOHANNES H, SIVAL, DEBORAH A
Published in Developmental medicine and child neurology (01.01.2012)
Published in Developmental medicine and child neurology (01.01.2012)
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GRIN2A-related disorders: genotype and functional consequence predict phenotype
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
Published in Brain (London, England : 1878) (01.01.2019)
Published in Brain (London, England : 1878) (01.01.2019)
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Acute flaccid myelitis and enterovirus D68: lessons from the past and present
Helfferich, Jelte, Knoester, Marjolein, Van Leer-Buter, Coretta C., Neuteboom, Rinze F., Meiners, Linda C., Niesters, Hubert G., Brouwer, Oebele F.
Published in European journal of pediatrics (01.09.2019)
Published in European journal of pediatrics (01.09.2019)
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Comparison of acute flaccid myelitis and transverse myelitis in children and evaluation of diagnostic criteria
Helfferich, Jelte, Bruijstens, Arlette L., Knoester, Marjolein, Brouwer, Oebele F., Neuteboom, Rinze F.
Published in European journal of neurology (01.08.2023)
Published in European journal of neurology (01.08.2023)
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Neurofibromatosis type 1 associated low grade gliomas: A comparison with sporadic low grade gliomas
Helfferich, Jelte, Nijmeijer, Ronald, Brouwer, Oebele F, Boon, Maartje, Fock, Annemarie, Hoving, Eelco W, Meijer, Lisethe, den Dunnen, Wilfred F.A, de Bont, Eveline S.J.M
Published in Critical reviews in oncology/hematology (01.08.2016)
Published in Critical reviews in oncology/hematology (01.08.2016)
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Twenty-nine Cases of Enterovirus-D68-associated Acute Flaccid Myelitis in Europe 2016: A Case Series and Epidemiologic Overview
Knoester, Marjolein, Helfferich, Jelte, Poelman, Randy, Van Leer-Buter, Coretta, Brouwer, Oebele F, Niesters, Hubert G M
Published in The Pediatric infectious disease journal (01.01.2019)
Published in The Pediatric infectious disease journal (01.01.2019)
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Dystonia in children and adolescents: a systematic review and a new diagnostic algorithm
van Egmond, Martje E, Kuiper, Anouk, Eggink, Hendriekje, Sinke, Richard J, Brouwer, Oebele F, Verschuuren-Bemelmans, Corien C, Sival, Deborah A, Tijssen, Marina A J, de Koning, Tom J
Published in Journal of neurology, neurosurgery and psychiatry (01.07.2015)
Published in Journal of neurology, neurosurgery and psychiatry (01.07.2015)
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Book Review
Neonatal loss of motor function in human spina bifida aperta
Sival, Deborah A, van Weerden, Tiemen W, Vles, Johan S H, Timmer, Albert, den Dunnen, Wilfred F A, Staal-Schreinemachers, A L, Hoving, Eelco W, Sollie, Krystyne M, Kranen-Mastenbroek, Vivianne J M, Sauer, Pieter J J, Brouwer, Oebele F
Published in Pediatrics (Evanston) (01.08.2004)
Published in Pediatrics (Evanston) (01.08.2004)
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Levetiracetam Monotherapy in Children with Epilepsy: A Systematic Review
Weijenberg, Amerins, Brouwer, Oebele F., Callenbach, Petra M. C.
Published in CNS drugs (01.05.2015)
Published in CNS drugs (01.05.2015)
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A novel diagnostic approach to patients with myoclonus
Zutt, Rodi, van Egmond, Martje E., Elting, Jan Willem, van Laar, Peter Jan, Brouwer, Oebele F., Sival, Deborah A., Kremer, Hubertus P., de Koning, Tom J., Tijssen, Marina A.
Published in Nature reviews. Neurology (01.12.2015)
Published in Nature reviews. Neurology (01.12.2015)
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Functional ability and muscle force in healthy children and ambulant Duchenne muscular dystrophy patients
Beenakker, Ernesto A.C., Maurits, Natalia M., Fock, Johanna M., Brouwer, Oebele F., van der Hoeven, Johannes H.
Published in European journal of paediatric neurology (01.01.2005)
Published in European journal of paediatric neurology (01.01.2005)
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Neuronal antibodies in pediatric epilepsy: Clinical features and long‐term outcomes of a historical cohort not treated with immunotherapy
Wright, Sukhvir, Geerts, Ada T., Jol‐van der Zijde, Cornelia Maria, Jacobson, Leslie, Lang, Bethan, Waters, Patrick, Tol, Maarten J. D., Stroink, Hans, Neuteboom, Rinze F., Brouwer, Oebele F., Vincent, Angela
Published in Epilepsia (Copenhagen) (01.05.2016)
Published in Epilepsia (Copenhagen) (01.05.2016)
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A post hoc study on gene panel analysis for the diagnosis of dystonia
van Egmond, Martje E., Lugtenberg, Coen H.A., Brouwer, Oebele F., Contarino, Maria Fiorella, Fung, Victor S.C., Heiner‐Fokkema, M. Rebecca, van Hilten, Jacobus J., van der Hout, Annemarie H., Peall, Kathryn J., Sinke, Richard J., Roze, Emmanuel, Verschuuren‐Bemelmans, Corien C., Willemsen, Michel A., Wolf, Nicole I., Tijssen, Marina A., de Koning, Tom J.
Published in Movement disorders (01.04.2017)
Published in Movement disorders (01.04.2017)
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Early onset facioscapulohumeral dystrophy – a systematic review using individual patient data
Goselink, Rianne J.M., Voermans, Nicol C., Okkersen, Kees, Brouwer, Oebele F., Padberg, George W., Nikolic, Ana, Tupler, Rossella, Dorobek, Malgorzata, Mah, Jean K., van Engelen, Baziel G.M., Schreuder, Tim H.A., Erasmus, Corrie E.
Published in Neuromuscular disorders : NMD (01.12.2017)
Published in Neuromuscular disorders : NMD (01.12.2017)
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