1Ion channels and genetic epilepsyKONG Wei-jing, JIANG Yu-wuSYMPOSIUM481-4872Clinical and molecular genetic study of epilepsy related to fever sensitivityZHANG Yue-huaSYMPOSIUM487-4913Diagnosis and treatment of gene mutation in early-onset epileptic encephalopathiesZHANG Yun-jian, ZHOU Shui-zhenSYMPOSIUM492-4974Molecular genetic research, diagnosis and treatment of benign familial infantile epilepsyWANG HuaSYMPOSIUM497-5015The genetic research, diagnosis and treatment of infantile spasmsWANG Ji-wenSYMPOSIUM502-5066Clinical and molecular genetic study of epilepsy related to glucose transporter type 1 deficiency syndromeZHANG Shi-min, BAO Xin-huaSYMPOSIUM506-5117@@512-5148Presurgical evaluation of epilepsy surgery in children : development and challengeLIU Xiao-yan, CAI Li-xinLECTURES515-5209The clinical and EEG characteristics of fulminant SSPE in childrenORIGINAL CONTRIBUTIONS521-52610Characteristics of covert reflexive visual spatial attention in children with attention-deficit/hyperactivity disorder with or without learning disabilitiesORIGINAL CONTRIBUTIONS527-53011Relationship between the expression levels of TGF-β1 and IL-18 mRNA and hormone resistance in children with primary nephrotic syndrome.ZHANG Bi-li, LIU Tao, WANG JianORIGINAL CONTRIBUTIONS531-53412Clinical research and genetic analysis of six cases of Xp21 contiguous gene deletion syndromeWANG Xu, WU Di, FANG Fang, JIANG MinORIGINAL CONTRIBUTIONS535-53913Clinical and imaging characteristics of cerebral paragonimiasis in childrenZHANG Gao-feng, LIU Heng, XI Shan-shanORIGINAL CONTRIBUTIONS540-54314@@544-54615@@547-54916Research progress of the pathogenesis of sepsis-associated encephalopathyXIANG Dan, ZENG Qi-yiSUMMARY550-55517Research progress of the renal damage in children with Wilson's diseaseWANG Xiao-lang, YAO YongSUMMARY556-55818One case of epileptic encephalopathy associated with cyclin-dependent kinase-like 5 gene mutationCASE REPORT559-56019@@中插1,555 