Idiopathic Partial Epilepsies

作者: Freedom F. Perkins

DOI: 10.1002/9781119998600.CH16

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参考文章(21)
Anne T. Berg, Ingrid E. Scheffer, New concepts in classification of the epilepsies: Entering the 21st century Epilepsia. ,vol. 52, pp. 1058- 1062 ,(2011) , 10.1111/J.1528-1167.2011.03101.X
Nicola Specchio, Federico Vigevano, The spectrum of benign infantile seizures Epilepsy Research. ,vol. 70, pp. 156- 167 ,(2006) , 10.1016/J.EPLEPSYRES.2006.01.018
Steven L. Kugler, Bhavna Bali, Philip Lieberman, Lisa Strug, Bernadine Gagnon, Peregrine L. Murphy, Tara Clarke, David A. Greenberg, Deb K. Pal, An autosomal dominant genetically heterogeneous variant of rolandic epilepsy and speech disorder Epilepsia. ,vol. 49, pp. 1086- 1090 ,(2008) , 10.1111/J.1528-1167.2007.01517.X
Roberto Caraballo, Michael Koutroumanidis, Chrysostomos P. Panayiotopoulos, Natalio Fejerman, Idiopathic childhood occipital epilepsy of Gastaut: a review and differentiation from migraine and other epilepsies. Journal of Child Neurology. ,vol. 24, pp. 1536- 1542 ,(2009) , 10.1177/0883073809332395
Chrysostomos P. Panayiotopoulos, Autonomic seizures and autonomic status epilepticus peculiar to childhood: diagnosis and management Epilepsy & Behavior. ,vol. 5, pp. 286- 295 ,(2004) , 10.1016/J.YEBEH.2004.01.013
P. A.D. Bouma, A. C. Bovenkerk, R. G.J. Westendorp, O. F. Brouwer, The course of benign partial epilepsy of childhood with centrotemporal spikes A meta-analysis Neurology. ,vol. 48, pp. 430- 437 ,(1997) , 10.1212/WNL.48.2.430
Kaate R. J. Vanmolkot, Esther E. Kors, Jouke-Jan Hottenga, Gisela M. Terwindt, Joost Haan, Wil A. J. Hoefnagels, David F. Black, Lodewijk A. Sandkuijl, Rune R. Frants, Michel D. Ferrari, Arn M. J. M. Van Den Maagdenberg, Novel mutations in the Na+, K+-ATPase pump gene ATP1A2 associated with familial hemiplegic migraine and benign familial infantile convulsions. Annals of Neurology. ,vol. 54, pp. 360- 366 ,(2003) , 10.1002/ANA.10674
John H. Livingston, J. Helen Cross, Ailsa Mclellan, Rachael Birch, Sameer M. Zuberi, A novel inherited mutation in the voltage sensor region of SCN1A is associated with Panayiotopoulos syndrome in siblings and generalized epilepsy with febrile seizures plus. Journal of Child Neurology. ,vol. 24, pp. 503- 508 ,(2009) , 10.1177/0883073808324537
Hiltrud Muhle, Carolien de Kovel, Carl Baker, Sarah von Spiczak, Katherine L Kron, Ines Steinich, Ailing A Kleefuß-Lie, Costin Leu, Verena Gaus, Bettina Schmitz, Karl M Klein, Philipp S Reif, Felix Rosenow, Yvonne Weber, Holger Lerche, Fritz Zimprich, Lydia Urak, Karoline Fuchs, Martha Feucht, Pierre Genton, Pierre Thomas, Frank Visscher, Gerrit-Jan de Haan, Rikke S Møller, Helle Hjalgrim, Daniela Luciano, Michael Wittig, Michael Nothnagel, Christian E Elger, Peter Nürnberg, Corrado Romano, Alain Malafosse, Bobby P C Koeleman, Dick Lindhout, Ulrich Stephani, Stefan Schreiber, Evan E Eichler, Thomas Sander, Ingo Helbig, Heather C Mefford, Andrew J Sharp, Michel Guipponi, Marco Fichera, Andre Franke, 15q13.3 microdeletions increase risk of idiopathic generalized epilepsy Nature Genetics. ,vol. 41, pp. 160- 162 ,(2009) , 10.1038/NG.292