Issue Date | Title | Author(s) |
2009 | Dravet syndrome or genetic (generalized) epilepsy with febrile seizures plus? | Scheffer, Ingrid E.; Zhang, Yue-Hua; Jansen, Floor E.; Dibbens, Leanne |
2010 | Generalized epilepsy with febrile seizures plus and classical idiopathic generalized epilepsy | Zhang, Yue-Hua; Scheffer, Ingrid |
2017 | Genetic epilepsy with febrile seizures plus Refining the spectrum | Zhang, Yue-Hua; Burgess, Rosemary; Malone, Jodie P.; Glubb, Georgie C.; Helbig, Katherine L.; Vadlamudi, Lata; Kivity, Sara; Afawi, Zaid; Bleasel, Andrew; Grattan-Smith, Padraic; Grinton, Bronwyn E.; Bellows, Susannah T.; Vears, Danya F.; Damiano, John A.; Goldberg-Stern, Hadassa; Korczyn, Amos D.; Dibbens, Leanne M.; Ruzzo, Elizabeth K.; Hildebrand, Michael S.; Berkovic, Samuel F.; Scheffer, Ingrid E. |
2010 | Genetics of the epilepsies: Genetic twists in the channels and other tales | Scheffer, Ingrid E.; Zhang, Yue-Hua; Gecz, Jozef; Dibbens, Leanne |
2012 | Genotype/phenotype of 6 Chinese cases with Niemann-Pick disease type C | Xiong, Hui; Higaki, Katsumi; Wei, Cui-jie; Bao, Xin-Hua; Zhang, Yue-Hua; Fu, Na; Qin, Jiong; Adachi, Kaori; Kumura, Yumiko; Ninomiya, Haruaki; Nanba, Eiji; Wu, Xi-Ru |
2017 | ILAE classification of the epilepsies: Position paper of the ILAE Commission for Classification and Terminology | Scheffer, Ingrid E.; Berkovic, Samuel; Capovilla, Giuseppe; Connolly, Mary B.; French, Jacqueline; Guilhoto, Laura; Hirsch, Edouard; Jain, Satish; Mathern, Gary W.; Moshe, Solomon L.; Nordli, Douglas R.; Perucca, Emilio; Tomson, Torbjoern; Wiebe, Samuel; Zhang, Yue-Hua; Zuberi, Sameer M. |
2018 | ILAE classification of the epilepsies: position paper of the ILAE Commission for Classification and Terminology | Scheffer, Ingrid E.; Berkovic, Samuel; Capovilla, Guiseppe; Connolly, Mary B.; French, Jacqueline; Guilhoto, Laura; Hirsch, Edouard; Jain, Satish; Mathern, Gary W.; Moshe, Solomon L.; Nordli, Douglas R.; Perucca, Emilio; Tomson, Torbjorn; Wiebe, Samuel; Zhang, Yue-Hua; Zuberi, Sameer M. |
Nov-2020 | NEXMIF encephalopathy: an X-linked disorder with male and female phenotypic patterns | Stamberger, Hannah; Hammer, Trine B.; Gardella, Elena; Vlaskamp, Danique R. M.; Bertelsen, Birgitte; Mandelstam, Simone; de Lange, Iris; Zhang, Jing; Myers, Candace T.; Fenger, Christina; Afawi, Zaid; Fuerte, Edith P. Almanza; Andrade, Danielle M.; Balcik, Yunus; Ben Zeev, Bruria; Bennett, Mark F.; Berkovic, Samuel F.; Isidor, Bertrand; Bouman, Arjan; Brilstra, Eva; Busk, Oyvind L.; Cairns, Anita; Caumes, Roseline; Chatron, Nicolas; Dale, Russell C.; de Geus, Christa; Edery, Patrick; Gill, Deepak; Granild-Jensen, Jacob Bie; Gunderson, Lauren; Gunning, Boudewijn; Heimer, Gali; Helle, Johan R.; Hildebrand, Michael S.; Hollingsworth, Georgie; Kharytonov, Volodymyr; Klee, Eric W.; Koeleman, Bobby P. C.; Koolen, David A.; Korff, Christian; Kury, Sebastien; Lesca, Gaetan; Lev, Dorit; Leventer, Richard J.; Mackay, Mark T.; Macke, Erica L.; McEntagart, Meriel; Mohammad, Shekeeb S.; Monin, Pauline; Montomoli, Martino; Morava, Eva; Moutton, Sebastien; Muir, Alison M.; Parrini, Elena; Procopis, Peter; Ranza, Emmanuelle; Reed, Laura; Reif, Philipp S.; Rosenow, Felix; Rossi, Massimiliano; Sadleir, Lynette G.; Sadoway, Tara; Schelhaas, Helenius J.; Schneider, Amy L.; Shah, Krati; Shalev, Ruth; Sisodiya, Sanjay M.; Smol, Thomas; Stumpel, Connie T. R. M.; Stuurman, Kyra; Symonds, Joseph D.; Mau-Them, Frederic Tran; Verbeek, Nienke; Verhoeven, Judith S.; Wallace, Geoffrey; Yosovich, Keren; Zarate, Yuri A.; Zerem, Ayelet; Zuberi, Sameer M.; Guerrini, Renzo; Mefford, Heather C.; Patel, Chirag; Zhang, Yue-Hua; Moller, Rikke S.; Scheffer, Ingrid E. |
2012 | Niemann-Pick disease type C: analysis of 7 patients | Xiong, Hui; Bao, Xin-Hua; Zhang, Yue-Hua; Xu, You-Ning; Qin, Jiong; Shi, Hui-Ping; Wu, Xi-Ru |
Jan-2023 | PACS gene family-related neurological diseases: limited genotypes and diverse phenotypes | Zhang, Han; Gao, Kai; Wang, Shuang; Zhang, Yue-Hua; Yang, Zhi-Xian; Wu, Ye; Jiang, Yu-Wu |
2018 | Severe infantile onset developmental and epileptic encephalopathy caused by mutations in autophagy gene WDR45 | Carvill, Gemma L.; Liu, Aijie; Mandelstam, Simone; Schneider, Amy; Lacroix, Amy; Zemel, Matthew; McMahon, Jacinta M.; Bello-Espinosa, Luis; Mackay, Mark; Wallace, Geoffrey; Waak, Michaela; Zhang, Jing; Yang, Xiaoling; Malone, Stephen; Zhang, Yue-Hua; Mefford, Heather C.; Scheffer, Ingrid E. |
2013 | The Impact of Health on Work in China: A Study Using Pilot Survey Data | Zhang, Yue-Hua; Li, Chu-Shiu; Liu, Chwen-Chi; Peng, Sheng-Chang |