PublisherDOIYearVolumeIssuePageTitleAuthor(s)Link
Annals of Child Neurology10.26815/acn.2019.0006620192712-12Frequently Identified Genetic Developmental and Epileptic Encephalopathy: A Review Focusing on Precision MedicineAra Ko, Hoon-Chul Kanghttp://annchildneurol.org/upload/pdf/acn-2019-00066.pdf, http://annchildneurol.org/journal/view.php?doi=10.26815/acn.2019.00066, http://annchildneurol.org/upload/pdf/acn-2019-00066.pdf
Developmental Medicine & Child Neurology10.1111/j.1469-8749.2010.03889.x2011534354-360CDKL5 gene-related epileptic encephalopathy: electroclinical findings in the first year of lifeFEDERICO MELANI, DAVIDE MEI, TIZIANA PISANO, SALVATORE SAVASTA, EMILIO FRANZONI, ANNA RITA FERRARI, CARLA MARINI, RENZO GUERRINIhttps://api.wiley.com/onlinelibrary/tdm/v1/articles/10.1111%2Fj.1469-8749.2010.03889.x, http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1469-8749.2010.03889.x/fullpdf
Annals of Child Neurology10.26815/acn.2020.00227202129143-46Precision Medicine Based on High-Throughput Nucleotide Sequencing for a Patient with SCN2A-Related Developmental Epileptic EncephalopathySe Eun Park, Dajeong Lee, Joo Young Song, Jeehun Lee, Jiwon Leehttp://annchildneurol.org/upload/pdf/acn-2020-00227.pdf, http://annchildneurol.org/journal/view.php?doi=10.26815/acn.2020.00227, http://annchildneurol.org/upload/pdf/acn-2020-00227.pdf
Meta Gene10.1016/j.mgene.2021.100953202130100953Whole exome sequencing identified a novel homozygous ARV1 mutation in an Iranian family with developmental and epileptic encephalopathy-38Emran Esmaeilzadeh, Sahar Bayat, Reza Mirfakhraie, Milad Gholamihttps://api.elsevier.com/content/article/PII:S2214540021001043?httpAccept=text/xml, https://api.elsevier.com/content/article/PII:S2214540021001043?httpAccept=text/plain
Russian Journal of Child Neurology10.17650/2073-8803-2021-16-1-2-10-412021161-210-41Genetic epilepsy caused by CDKL5 gene mutations as an example of epileptic encephalopathy and developmental encephalopathy: literature review and own observationsK. Yu. Mukhin, O. A. Pylaeva, M. Yu. Bobylova, V. A. Chadaevhttps://rjdn.abvpress.ru/jour/article/viewFile/360/242
Developmental Medicine & Child Neurology10.1111/dmcn.152192022648935-935Quality of lives matter in developmental and epileptic encephalopathyFrancesca Sofiahttps://onlinelibrary.wiley.com/doi/pdf/10.1111/dmcn.15219, https://onlinelibrary.wiley.com/doi/full-xml/10.1111/dmcn.15219, https://onlinelibrary.wiley.com/doi/pdf/10.1111/dmcn.15219
Developmental Medicine & Child Neurology10.1111/j.1469-8749.1998.tb15408.x2008408508-516Epileptic aphasia: a consequence of regional hypometabolic encephalopathy?ME O'Regan, JK Brown, GM Goodwin, M. Clarkehttps://api.wiley.com/onlinelibrary/tdm/v1/articles/10.1111%2Fj.1469-8749.1998.tb15408.x, http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1469-8749.1998.tb15408.x/fullpdf
Developmental Medicine & Child Neurology10.1111/j.1469-8749.1987.tb02512.x2008294520-528EARLY INFANTILE EPILEPTIC ENCEPHALOPATHY WITH SUPPRESSION BURST: OHTAHARA SYNDROMEM. Clarke, J. Gill, M. Noronha, I. McKinlayhttps://api.wiley.com/onlinelibrary/tdm/v1/articles/10.1111%2Fj.1469-8749.1987.tb02512.x, http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1469-8749.1987.tb02512.x/fullpdf
Developmental Medicine & Child Neurology10.1111/j.1469-8749.2010.03888.x2011534296-297CDKL5 gene-related epileptic encephalopathy: electroclinical findings in the first year of lifeWILLEM F M ARTShttps://api.wiley.com/onlinelibrary/tdm/v1/articles/10.1111%2Fj.1469-8749.2010.03888.x, http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1469-8749.2010.03888.x/fullpdf
10.21203/rs.3.rs-257334/v12021Phenotypic Spectrum and Long-term Outcome in Children With Genetic Causes of Early-onset Epileptic EncephalopathyChunhui Hu, Deying Liu, Tian Luo, Yi Wang, Zhisheng Liuhttps://www.researchsquare.com/article/rs-257334/v1, https://www.researchsquare.com/article/rs-257334/v1.html