EPIDEMIOLOGY
Soumen Khatua(St Nicholas Hospital), Thomas S. Jacques(Great Ormond Street Hospital), Stefan Rutkowski(Universität Hamburg), André O. von Bueren(University of Geneva), Kōichi Mishima, Claudia E. Kuehni(University of Bern), Zsuzsanna Jakab(Semmelweis University), Óscar Zurriaga(Fundación para el Fomento de la Investigación Sanitaria y Biomédica de la Comunitat Valenciana), Corrie Gidding(Radboud University Nijmegen), Marjolijn C.J. Jongmans(Utrecht University), Tomohiro Koga(Beth Israel Deaconess Medical Center), Marjolijn J. L. Ligtenberg(Radboud University Nijmegen), Bernard Lacour, Tribhawan S. Vats(University of South Florida), D Sommelet, Ryutaro Nishikawa(Nagoya City University), Debi Nelson, Fernando Moreno(Hospital Clínico San Carlos), Takamitsu Fujimaki, Mireia Vicente, Jun Adachi(Otsuka (Japan)), Matthew G.K. Benesch, Kenji Wakiya, Pieter Wesseling(Radboud University Nijmegen), Masaharu Nishi, Julie Von Behren, C Stiller, Rafael Peris‐Bonet(Hospital Universitari i Politècnic La Fe), Robert W. Brown(Creative Research Enterprises (United States)), Tetsu Yanagisawa, Henrik Hasle(Aarhus University Hospital), Kohei Fukuoka(Hospital for Sick Children), Takeshi Suzuki, Maria Luisa Garrè(Istituto Giannina Gaslini), N. von der Weid(University of Geneva), Christian Rickert, Jolanda Schieving, Daniel Satgé, Mark D. Pearlman(University of Michigan), Maura Massimino(Fondazione IRCCS Istituto Nazionale dei Tumori), M Matsutani, Sarah Leigh Nicholson, K. Robson, Maurice Greenberg, Marcel Vekemans, S Sullivan, Stephen Crosier(Newcastle upon Tyne Hospitals NHS Foundation Trust), Patricia M. Reynolds, Paul G. Fisher(Northwestern University)
Cited by 1
Related Papers
The clinicopathologic spectrum of focal cortical dysplasias: A consensus classification proposed by an ad hoc Task Force of the ILAE Diagnostic Methods Commission1
|Epilepsia|2010|1.7k
Analysis of the mouse transcriptome based on functional annotation of 60,770 full-length cDNAs
|Nature|2002|1.6k
Overcoming the blood–brain tumor barrier for effective glioblastoma treatment
|Drug Resistance Updates|2015|1k
Heritable somatic methylation and inactivation of MSH2 in families with Lynch syndrome due to deletion of the 3′ exons of TACSTD1
|Nature Genetics|2008|818
<scp>WHO</scp> 2016 Classification of gliomas
|Neuropathology and Applied Neurobiology|2017|817