Epilepsy Epileptic Syndromes and Treatment

被引：46
作者：
Katyayan, Akshat [1 ,2 ]
Diaz-Medina, Gloria [1 ,2 ]
机构：
[1] Texas Childrens Hosp, Baylor Coll Med, Dept Pediat, 6701 Fannin St,Suite 1250, Houston, TX 77030 USA
[2] Texas Childrens Hosp, Baylor Coll Med, Dept Neurol, 6701 Fannin St,Suite 1250, Houston, TX 77030 USA
来源：
NEUROLOGIC CLINICS | 2021年 / 39卷 / 03期
关键词：
Epilepsy; Epilepsy syndrome; Infantile spasms; Lennox-Gastaut syndrome; Childhood absence epilepsy; Juvenile myoclonic epilepsy; Childhood epilepsy with centrotemporal spikes; Dravet syndrome; JUVENILE MYOCLONIC EPILEPSY; KINGDOM INFANTILE SPASMS; DRAVET SYNDROME; ILAE COMMISSION; POSITION PAPER; CLINICAL-TRIAL; MANAGEMENT; MULTICENTER; VIGABATRIN; CLASSIFICATION;
D O I：
10.1016/j.ncl.2021.04.002
中图分类号：
R74 [神经病学与精神病学];
学科分类号：
摘要：
[No abstract available]
引用
收藏
页码：779 / 795
页数：17
相关论文
共 35 条
[1]   ATYPICAL BENIGN PARTIAL EPILEPSY OF CHILDHOOD [J].
AICARDI, J ;
CHEVRIE, JJ .
DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY, 1982, 24 (03) :281-292
[2]   Lennox-Gastaut syndrome: a consensus approach on diagnosis, assessment, management, and trial methodology [J].
Arzimanoglou, Alexis ;
French, Jacqueline ;
Blume, Warren T. ;
Cross, J. Helen ;
Ernst, Jan-Peter ;
Feucht, Martha ;
Genton, Pierre ;
Guerrini, Renzo ;
Kluger, Gerhard ;
Pellock, John M. ;
Perucca, Emilio ;
Wheless, James W. .
LANCET NEUROLOGY, 2009, 8 (01) :82-93
[3]   Modern management of juvenile myoclonic epilepsy [J].
Brodie, Martin J. .
EXPERT REVIEW OF NEUROTHERAPEUTICS, 2016, 16 (06) :681-688
[4]   De novo mutations in the sodium-channel gene SCN1A cause severe myoclonic epilepsy of infancy [J].
Claes, L ;
Del-Favero, J ;
Ceulemans, B ;
Lagae, L ;
Van Broeckhoven, C ;
De Jonghe, P .
AMERICAN JOURNAL OF HUMAN GENETICS, 2001, 68 (06) :1327-1332
[5]   Dravet Syndrome: Diagnosis and Long-Term Course [J].
Connolly, Mary B. .
CANADIAN JOURNAL OF NEUROLOGICAL SCIENCES, 2016, 43 :S3-S8
[6]   Panayiotopoulos syndrome: A benign childhood autonomic epilepsy frequently imitating encephalitis, syncope, migraine, sleep disorder, or gastroenteritis [J].
Covanis, Athanasios .
PEDIATRICS, 2006, 118 (04) :E1237-E1243
[7]   Dravet syndrome: Treatment options and management of prolonged seizures [J].
Cross, J. Helen ;
Caraballo, Roberto H. ;
Nabbout, Ritna ;
Vigevano, Federico ;
Guerrini, Renzo ;
Lagae, Lieven .
EPILEPSIA, 2019, 60 :S39-S48
[8]   JUVENILE MYOCLONIC EPILEPSY OF JANZ [J].
DELGADOESCUETA, AV ;
ENRILEBACSAL, F .
NEUROLOGY, 1984, 34 (03) :285-294
[9]   The core Dravet syndrome phenotype [J].
Dravet, Charlotte .
EPILEPSIA, 2011, 52 :3-9
[10]   Atypical rolandic epilepsy [J].
Fejerman, Natalio .
EPILEPSIA, 2009, 50 :9-12
1234