Myoclonic status epilepticus in the elderly: Clinical vignettes of four patients [0.03%]
老年人肌阵挛性癫痫持续状态：四个病例的临床表现
Melek Kandemir Yılmaz,Özgür Öztop Çakmak,İrem Erkent et al.
Melek Kandemir Yılmaz et al.
Infantile epileptic spasms syndrome secondary to diffuse low-grade glioma, MAPK pathway-altered: The importance of early surgical intervention [0.03%]
儿童期散发低级别胶质瘤型癫痫性脑病的早期手术干预的重要性
Yusuke Ikeda,Kiyohiro Kim,Shu Hamada et al.
Yusuke Ikeda et al.
The role of SCN1A mutations in temporal lobe epilepsy: Genetic insights and clinical implications [0.03%]
SCN1A基因突变在颞叶癫痫中的作用：遗传学见解与临床意义
Bassel Alrabadi,Hasan Matar,Mahmoud Marouf et al.
Bassel Alrabadi et al.
Purpose: Temporal lobe epilepsy (TLE) is the most common focal epilepsy, yet the genetic mechanisms underlying its development remain incompletely understood. The sodium channel gene SCN1A, known to be involved in several...
Anatomo-clinical correlations in patients with lateral occipital seizures: A systematic review [0.03%]
外侧枕叶癫痫患者的临床和解剖相关性系统回顾
Mathilde Chipaux,Rayann Checri,Emmanuel Raffo
Mathilde Chipaux
Objective: Epilepsies presenting with lateral occipital seizures (LOS) pose diagnostic challenges due to their rarity and association with complex visual symptoms. We performed a systematic review to characterize the icta...
Unique EEG signature of atypical absence seizures in SYNGAP1-related developmental and epileptic encephalopathy [0.03%]
SYNGAP1相关性发育和癫痫性脑病患儿不典型失神发作的EEG特征
Rainier Mark Loidor L Rapal,Joshua Chang,Douglas Nordli rd
Rainier Mark Loidor L Rapal
Glioma-related epilepsy in patients with oligodendroglioma, IDH-mutant, and 1p/19q-codeleted: A single-institute study [0.03%]
单中心IDH突变型少枝胶质瘤伴1p/19q联合缺失患者的胶母细胞相关性癫痫研究
Jiajia Liu,Yu Song,Jiahan Dong et al.
Jiajia Liu et al.
Purpose: The current study aimed to investigate the clinical correlation of glioma-related epilepsy (GRE) in patients with IDH-mutant and 1p/19q-codeleted oligodendrogliomas. ...
Impact of vitamin D supplementation and status on seizure frequency and quality of life in drug-resistant epilepsy: A systematic review and meta-analysis [0.03%]
维生素D补充剂的摄入与状态对难治性癫痫发作频率及生活质量影响的系统评价和meta分析
Bassel Alrabadi,Hasan I Matar,Natalie Bandak et al.
Bassel Alrabadi et al.
Background: Drug-resistant epilepsy (DRE) affects approximately one-third of patients with epilepsy and is associated with significant morbidity and reduced quality of life. Emerging evidence suggests that vitamin D may i...
Cook4Keto: Bridging culinary expertise and clinical practice to improve adherence to ketogenic diet therapy in drug-refractory epilepsy [0.03%]
Cook4Keto：弥合烹饪专业知识和临床实践之间的差距，以改善药物难治性癫痫患者生酮饮食疗法的依从性
G Castellucci,A Calka,R Pedapati et al.
G Castellucci et al.
Distinct phenotypes differentiate paroxysmal kinesigenic dyskinesia from epilepsy in children with PRRT2 variants [0.03%]
具有PRRT2变异儿童的阵发性运动诱发性 dystonia 和癫痫的不同表型特征
Xiaoang Sun,Liqun Geng,Xuqin Chen
Xiaoang Sun
Objective: PRRT2 gene variations are commonly associated with paroxysmal kinesigenic dyskinesia (PKD) and epilepsy (EP). This study compares the clinical phenotypes of PKD and EP in relation to PRRT2, focusing on the asso...
Photosensitive infantile spasms in a preterm infant with 4q22.3-q24 deletion involving PPP3CA [0.03%]
包含PPP3CA基因的4q22.3-q24缺失导致早产儿光敏感性婴儿痉挛症
Odette El Ghawi,Debopam Samanta,Sarah Cobb et al.
Odette El Ghawi et al.