Results 21 to 30 of about 974,404 (311)

KBG syndrome mimicking genetic generalized epilepsy [PDF]

, 2022
•Several conditions may mimic Genetic Generalized Epilepsy GGE. •GGE is less frequently misdiagnosed compared to other subtypes of epilepsy. •KBG syndrome is a rare autosomal dominant condition. •KBG syndrome may mimic GGE.
MJ Murphy (12708812), DJ Costello (10572470), Marie Greally (7895861), N McSweeney (12708815), Gianpiero Cavalleri (7895525), Katherine Benson (7895723)   +5 more
core   +3 more sources

Atypical juvenile myoclonic epilepsy with structural brain abnormalities and cognitive impairment: A case report [PDF]

Romanian Journal of Neurology, 2023
Juvenile myoclonic epilepsy (JME) is an idiopathic generalized epilepsy affecting 5–10% of epilepsy patients. Its exact cause remains unknown, but recent studies indicate frontal region involvement.
Putri Permata Sari, Prastiya Indra Gunawan, Riza Noviandi, Sunny Mariana Samosir   +3 more
doaj   +1 more source

Inherited Epilepsies

Bezmiâlem Science, 2020
Mutations in genes encoding the formation of ion channels may cause epileptic syndromes. These epileptic syndromes are generally divided into generalized and partial epilepsies.
Halil Aziz VELİOĞLU, Muhammed Yunus BEKTAY   +1 more
doaj   +1 more source

Role of neurotrophins and neuropeptides in Genetic Absence Epilepsy Rats from Strasbourg (GAERS) : a model for human generalized absence seizures [PDF]

, 2010
Several studies have shown that neurotrophins and neuropeptides contribute to epileptogenesis but their impact on idiopathic generalized epilepsies is not yet elucidated.
Landweer, Svenja
core   +1 more source

The Coexistence of Idiopathic Generalized Epilepsy and Partial Epilepsy [PDF]

Epilepsia, 2004
Summary:  Purpose: To describe the clinical, EEG, and imaging data of a series of patients with features of both idiopathic generalized epilepsy (IGE) and partial epilepsy. Methods: A computerized database of all patients attending the regional epilepsy clinic was used to identify all patients with IGE.
Andrew, Nicolson, David W, Chadwick, David F, Smith   +2 more
openaire   +2 more sources

Role of circulating miR 194-5p, miR 106b, and miR 146a as potential biomarkers for epilepsy: a case-control study

The Egyptian Journal of Neurology, Psychiatry and Neurosurgery, 2020
Background Epilepsy is a chronic neurological disease. A suitable biomarker for epilepsy diagnosis remains lacking. MicroRNAs (miRNAs) were pronounced as promising biomarkers for epileptogenesis. Objectives To analyze the expression levels of miR 194-5p,
Mervat Moustafa, Noha T. Abokrysha, Nermeen A. Eldesoukey, Dalia Gamil Amin, Nesma Mounir, Dalia M. Labib   +5 more
doaj   +1 more source

A Classification Model of EEG Signals Based on RNN-LSTM for Diagnosing Focal and Generalized Epilepsy

Sensors, 2022
Epilepsy is a chronic neurological disorder caused by abnormal neuronal activity that is diagnosed visually by analyzing electroencephalography (EEG) signals.
Tahereh Najafi, Rosmina Jaafar, Rabani Remli, Wan Asyraf Wan Zaidi   +3 more
doaj   +1 more source

CHD2 variants are a risk factor for photosensitivity in epilepsy. [PDF]

, 2015
Photosensitivity is a heritable abnormal cortical response to flickering light, manifesting as particular electroencephalographic changes, with or without seizures. Photosensitivity is prominent in a very rare epileptic encephalopathy due to de novo CHD2
Cantonetti, L., Muhle, H., Thiele, H., Lench, N, Krishna Chinthapalli, V, Krause, R, Sadleir, L. G., Moller, R. S., EURO Epinomics CoGIE Consortium, Afrikanova, T, Jocic-Jakubi, B., Capovilla, G., Myers, C., Myers, C. T., Sadleir, LG, Muhle, H, Nürnberg, P, Helbig, I., Parisi, P., EuroEPINOMICS CoGIE Consortium,, Pendziwiat, M., Stephani, U., Coppola, A., Myers, CT, Chinthapalli, V. K., Stephani, U, Del Gaudio, L., De Kovel, CGF, Chinthapalli, VK, Veggiotti, P., Lehesjoki, AE, Jacmin, M., Drury, S., Piccioli, M., Berkovic, S. F., Esguerra, C., Trenite, D., Chinthapalli, V., Thiele, H, Kasteleijn-Nolst Trenité, DG, Lehesjoki, A., Crawford, A., Boustred, C., Lerche, H, Moller, R., Galizia, E. C., Ruppert, A. -K., Helbig, I, Schubert, J, Schneider, A. L., Crawford, AD, Schubert, J., Veggotti, P, Esguerra, CV, Striano, S., Ruppert, A., Berkovic, S., Galizia, EC, Cordero-Maldonado, M., Leu, C., Mefford, H. C., Martins, T. G., Palotie, A, Crawford, A. D., Covanis, A., Sisodiya, S., Ruppert, AK, Cordero-Maldonado, M. L., Møller, RS, Esguerra, C. V., Trenité, D. G. A. K. -N., Schneider, A., Coppola, A, Cantonetti, L, Leu, C, Del Gaudio, L, Cordero-Maldonado, ML, De Kovel, C. G. F., Berkovic, SF, Mullen, S. A., Trenité, DGAKN, Martins, T., Koeleman, BPC, Jacmin, M, Covanis, A, Boustred, C, Moller, RS, Martins, TG, Sisodiya, SM, Koeleman, B., Sander, T, Sander, T., Nürnberg, P., Mullen, SA, Palotie, A., Pendziwiat, M, Parisi, P, Capovilla, G, Scheffer, I., Koeleman, BP, Gaudio, LD, Lerche, H., Mullen, S., Veggiotti, P, Scheffer, I. E., Koeleman, B. P. C., De Kovel, C., Piccioli, M, Sisodiya, S. M., Lehesjoki, A. -E., Afrikanova, T., de Kovel, CG, Mefford, HC, Drury, S, Scheffer, IE, Schneider, AL, Mefford, H., Krause, R., Galizia, E., Striano, S, Jocic-Jakubi, B, Lench, N., Sadleir, L.   +122 more
core   +1 more source

Juvenile myoclonic epilepsy as a spectrum disorder: A focused review

, 2021
In consequence of newer research juvenile myoclonic epilepsy (JME) is no longer seen as a homogeneous disease. The causes of the existing variance are only partially known yet.
Wolf, Peter, Baykan, BETÜL
core   +1 more source

Analysis of the effects of different provocative methods on bioelectrical brain activity in patients with epilepsy

Neurologijos seminarai, 2019
ntroduction. The sensitivity of EEG is increased by performing standard provocative tests. The effects of additional cognitive tasks on bioelectrical brain activity aren’t widely studied.
G. Seniut , D. Streckytė , R. Mameniškienė   +2 more
doaj   +1 more source