Results 91 to 100 of about 3,955,077 (290)

Dominant partial epilepsies: A clinical, electrophysiological and genetic study of 19 European families [PDF]

, 2017
Nineteen families with autosomal dominant partial epilepsy were analysed clinically and electrophysiologically in detail. Seventy-one patients were studied as well as 33 non-epileptic at-risk family members.
Marescaux, C., Thomas, P., Genton, P., An, I., Hirsch, E., Vigevano, F., Gericke, C. A., Rudolf, G., Brice, A., Baulac, S., Sebastianelli, R., LeGuern, E., Picard, F., Kahane, P., Herman, A., Guerrini, R.   +15 more
core  

Temporal Divergence of True and False Alarms in Pediatric Nocturnal Seizure Monitoring

Annals of Clinical and Translational Neurology, EarlyView.
The early‐morning surge in false seizure alarms supports exploring time‐ or state‐dependent detection thresholds to reduce false detections. ABSTRACT Seizure detection devices can improve the safety of children with epilepsy, yet high false alarms limit their clinical applicability.
Mohammad Shahbakhti, Anemoon T. Bosch, Job van der Palen, Franciscus S. Leijten, Johannes P. van Dijk, Richard H. C. Lazeron, Roland D. Thijs   +6 more
wiley   +1 more source

Dynamic imaging of coherent sources reveals different network connectivity underlying the generation and perpetuation of epileptic seizures [PDF]

, 2013
The concept of focal epilepsies includes a seizure origin in brain regions with hyper synchronous activity (epileptogenic zone and seizure onset zone) and a complex epileptic network of different brain areas involved in the generation, propagation, and ...
Raethjen, Jan, Günther Deuschl, Elshoff, Lydia, Lydia Elshoff, Abdul Rauf Anwar (475525), Stephani, Ulrich, Michael Siniatchkin, Abdul Rauf Anwar, Muthuraman Muthuraman (328846), Michael Siniatchkin (475526), Deuschl, Günther, Ulrich Stephani, Muthuraman Muthuraman, Günther Deuschl (58204), Jan Raethjen, Muthuraman, Muthuraman, Siniatchkin, Michael, Lydia Elshoff (475524), Ulrich Stephani (364671), Jan Raethjen (328852), Anwar, Abdul Rauf, Raethjen Jan, Elshoff Lydia, Stephani Ulrich, Anwar Abdul Rauf, Deuschl Günther, Siniatchkin Michael   +26 more
core   +2 more sources

Early Clinical and Cerebrospinal Fluid Predictors of 1‐Year Recurrence in Autoimmune GFAP Astrocytopathy

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective Autoimmune glial fibrillary acidic protein astrocytopathy (GFAP‐A) is an inflammatory central nervous system disorder with variable outcomes. Relapse occurs in a subset of patients, but early predictors remain unclear. We aimed to identify admission‐available features associated with 1‐year recurrence and develop an interpretable ...
Qingting Hong, Yuping Xiao, Yuhan Wu, Ziyuan Huang, Weishan Liang, Li Xiao, Yaqing Shu, Tingting Lu, Yanyu Chang, Wei Qiu, Yuge Wang   +10 more
wiley   +1 more source

Familial Partial Epilepsies [epilepsias Parciais Familiares]

, 2015
[No abstract available]583 B862868Ottmann, R., Lee, J.H., Risch, N., Clinical indicators of genetic susceptibility to epilepsy (1996) Epilepsia, 37, pp.
Kobayashi E., Scotoni A.E., Carvalho M.I., Guerreiro M.M., Cendes F., Guerreiro C.A.M., Sousa S.C., Lopes-Cendes I.   +7 more
core  

Levetiracetam as add-on therapy in generalised epilepsies

, 2004
Levetiracetam is highly effective as add-on treatment in refractory partial-onset seizures but there are only limited data supporting its benefit in generalised epilepsies.
Kumar, S. Pradeep, Smith, Philip E. M.
core   +1 more source

Mother and daughter with adolescent-onset severe frontal lobe dysfunction and epilepsy

Dementia & Neuropsychologia
Familial cases of early-onset prominent frontal lobe dysfunction associated with epilepsy have not been reported to date. We report a mother and her only daughter with incapacitating behavioral manifestations of frontal lobe dysfunction and epilepsy of ...
Giordani Rodrigues dos Passos, Alonso Cuadrado Fernández, Adriana Machado Vasques, William Alves Martins, André Palmini   +4 more
doaj   +1 more source

Complementing Engel Classification: Postoperative Scalp EEG as an Objective Indicator in SEEG‐Guided Radiofrequency Thermocoagulation—A Seizure‐Onset Pattern‐Based Stratified Analysis—

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Background Stereoelectroencephalography‐guided radiofrequency thermocoagulation (SEEG‐RFTC) is a minimally invasive therapy for drug‐resistant focal epilepsy. However, the relationship between specific seizure‐onset patterns (SOPs), particularly low‐voltage fast activity (LVFA), and postoperative scalp EEG normalization remains inadequately ...
Yi‐qing Yang, Rui Zhang, Haiyan Ma, Lu Yang, Xuefeng Qu, Qiqi Chen, Yan Zhang   +6 more
wiley   +1 more source

Clinical Variability and Genotype Driven Outcomes in an International Cohort of 14 Pediatric FIG4 Patients

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Background Biallelic FIG4 variants classically cause distinct conditions characterized by peripheral neuropathy (Charcot‐Marie‐Tooth disease type 4J) or skeletal dysplasia (Yunis‐Varón syndrome). However, central nervous system involvement is increasingly recognized. The prevalence and specific characteristics of movement disorders within FIG4‐
Andrea Gangfuß, Vykuntaraju K. Gowda, Daniel Natera‐de Benito, Pinki Munot, Maria Vanegas, Alejandra Darling, Constanze Reutlinger, Laura Carrera‐Garcia, Gilbert Wunderlich, Heike Kölbel, Burkhard Stüve, David Muhmann, Lucía Monfort Belenguer, Diana‐Gabriela Barca, Viveka Santhosh Reddy C, Varunvenkat M. Srinivasan, Cristina Molina Anguita, Heinz Jungbluth, Hormos Salimi Dafsari, Thomas Rossor, Johann Böhm, Ulrike Schara‐Schmidt, Andreas Roos   +22 more
wiley   +1 more source

The management of refractory idiopathic epilepsies

, 2001
Idiopathic epilepsies comprise a wide variety of partial and generalized syndromes that have in common a known or presumed genetic etiology and the lack of overt abnormalities other than the epilepsy itself. Most of these epilepsies have a benign natural
PERUCCA, EMILIO
core   +1 more source