A multimodal diagnostic approach for lateralised rhythmic delta activity in the ictal-interictal continuum [0.03%]
脑放电痫性活动的多模态诊断方法研究
Maddalena Spalletti,Francesca Pescini,Davide Gadda et al.
Maddalena Spalletti et al.
The ictal-interictal continuum represents a diagnostic challenge even for expert neurrophysiologists, often requiring an additional multimodal diagnostic workup to understand its clinical significance. Lateralised rhythmic delta activity (L...
James R Barnett,Bradley M Fleming,Kennedy R Geenen et al.
James R Barnett et al.
To characterize the clinical phenotype of Sunflower syndrome. Sunflower syndrome is a rare photosensitive epilepsy syndrome characterized by highly stereotyped seizures, photosensitivity, and heliotropism. We retrospectively reviewed the me...
Pitfalls in the diagnosis of Jeavons syndrome: a study of 32 cases and review of the literature [0.03%]
Jeavons综合征诊断陷阱及病例报道与文献复习
Aylin Reyhani,Çiğdem Özkara
Aylin Reyhani
Jeavons syndrome (JS) is mainly characterized by eyelid myoclonia with or without absences. It is thought to be underdiagnosed rather than have a rare prevalence. We aimed to investigate the electroclinical features of JS to determine possi...
Eslicarbazepine for focal epilepsy and acute intermittent porphyria [0.03%]
艾司卡巴锌治疗局灶性癫痫和急性间歇性血管内皮生长因子相关疾病
Tamara Herrera-Fortin,Raluca Pana,Ewa Wesolowska et al.
Tamara Herrera-Fortin et al.
Porphyrias are rare genetic disorders which cause a deficiency in the enzymes involved in the biosynthesis of heme. The treatment of epilepsy in patients with acute intermittent porphyria can be difficult since many anticonvulsants can incr...
Sensitivity of magnetoencephalography as a diagnostic tool for epilepsy: a prospective study [0.03%]
磁性脑成像作为诊断癫痫的工具的价值：一项前瞻性研究
Imte Koster,Pauly Ossenblok,Geert J Brekelmans et al.
Imte Koster et al.
The diagnostic process for epilepsy can be lengthy and stressful, which may delay the start of treatment. The objective of this study was to determine the benefit of routine magnetoencephalography (MEG) with regard to diagnostic gain, compa...
Joshua J Bear,Heidi E Kirsch,Brian D Berman et al.
Joshua J Bear et al.
Functional connectivity is providing new insights into the network nature of epilepsy with growing clinical applications. Our objective was to validate a novel magnetoencephalography-based method to non-invasively measure the epileptic netw...
Hussein Hamdi,Sebastien Boissonneau,Sofiene Hadidane et al.
Hussein Hamdi et al.
Drop attacks are the most responsive seizure type to open callosotomy, however, surgical complications can worsen the prognosis. Various less invasive techniques have been explored in an effort to minimize the risk. We present a patient who...
Reply to comment on "Indications and expectations for neuropsychological assessment in epilepsy surgery in children and adults" [0.03%]
关于“儿童和成人癫痫手术神经心理评估的指征和预期”的评论回复
Panayiotis Patrikelis,Giuliana Lucci,Athanasia Alexoudi et al.
Panayiotis Patrikelis et al.
Comparison of the effectiveness and tolerability of perampanel and brivaracetam: a real-world, observational, retrospective study [0.03%]
一项真实世界、观察性、回顾性研究比较了elperisent和brivaracetam的疗效和耐受性
Claudio Liguori,Natalia Manfredi,Rosaria Renna et al.
Claudio Liguori et al.
Perampanel (PER) and brivaracetam (BRV) are third-generation antiseizure medications. The aim of the present retrospective, double-centre study was to compare the effectiveness and tolerability between PER and BRV in adult patients with epi...
De novo truncating mutation in SCN1A as a cause of febrile seizures plus (FS+) [0.03%]
SCN1A基因的新发截短突变与发热性全面性癫痫发作相关
Alex Jaimes,Rosa Guerrero-López,Beatriz González-Giráldez et al.
Alex Jaimes et al.
SCN1A is one of the most relevant epilepsy genes. In general, de novo severe mutations, such as truncating mutations, lead to a classic form of Dravet syndrome (DS), while missense mutations are associated with both DS and milder phenotypes...