Levetiracetam Monotherapy in Children with Epilepsy: A Systematic Review

Por Weijenberg, Amerins, Brouwer, Oebele F., Callenbach, Petra M. C.
Publicado no CNS Drugs (2015)

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

Por Weijenberg, Amerins, Callenbach, Petra M. C., Brouwer, Oebele F.
Publicado no Epilepsia Open (2016)

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 no Child Neurol Open (2018)

Contextual Structured Reporting in Radiology: Implementation and Long-Term Evaluation in Improving the Communication of Critical Findings

Por Olthof, Allard W., Leusveld, Anne L. M., de Groot, Jan Cees, Callenbach, Petra M. C., van Ooijen, Peter M. A.
Publicado no J Med Syst (2020)

Mortality Risks in New-Onset Childhood Epilepsy

Por Berg, Anne T., Nickels, Katherine, Wirrell, Elaine C., Geerts, Ada T., Callenbach, Petra M.C., Arts, Willem F., Rios, Christina, Camfield, Peter R., Camfield, Carol S.
Publicado em 2013

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 no Epilepsia Open (2017)

Linkage and association analysis of CACNG3 in childhood absence epilepsy

Por Everett, Kate, Chioza, Barry, Aicardi, Jean, Aschauer, Harald, Brouwer, Oebele, Callenbach, Petra, Covanis, Athanasios, Dulac, Olivier, Eeg-Olofsson, Orvar, Feucht, Martha, Friis, Mogens, Goutieres, Françoise, Guerrini, Renzo, Heils, Armin, Kjeldsen, Marianne, Lehesjoki, Anna-Elina, Makoff, Andrew, Nabbout, Rima, Olsson, Ingrid, Sander, Thomas, Sirén, Auli, McKeigue, Paul, Robinson, Robert, Taske, Nichole, Rees, Michele, Gardiner, Mark
Publicado em 2007

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 em 2009

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 no Brain (2019)