Epileptic Disorders




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Issue Information

doi : 10.1002/epd2.20070

Volume 25, Issue 1

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Focal epilepsies: Update on diagnosis and classification

Fábio A. Nascimento, Daniel Friedman, Jurriaan M. Peters, Meriem K. Bensalem-Owen, Fernando Cendes, Stefan Rampp, Elaine Wirrell, Ingmar Blümcke, William Tatum, Sándor Beniczky

doi : 10.1002/epd2.20045

Correctly diagnosing and classifying seizures and epilepsies is paramount to ensure the delivery of optimal care to patients with epilepsy.

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Let food be thy medicine. The interaction between ketogenic diet therapy and anti-seizure medications: A systematic review

Marisa L. Armeno, Eric H. Kossoff

doi : 10.1002/epd2.20055

Ketogenic diet therapy (KDT) is a nonpharmacological treatment that has been demonstrated to be effective in reducing seizures in patients with drug-resistant epilepsy.

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The devil is in the details: Understanding how misinformation regarding epilepsy manifests in TikTok videos

Kallie Jiang, Douglas R. Nordli III, Fernando Galan

doi : 10.1002/epd2.20036

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Different relationships between epilepsy syndromes and autoimmune diseases

João Chaves, Bárbara Leal, Ana Sardoeira, Vanessa Carvalho, Raquel Samões, Joel Freitas, Rui Chorão, Ana Marta Ferreira, Sandra Brás, João Lopes, João Ramalheira, Carolina Lemos, Paulo Pinho Costa, António Marinho, Berta Martins da Silva, António Martins da Silva

doi : 10.1002/epd2.20048

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Impact of an optimized epilepsy surgery imaging protocol for focal epilepsy: A monocentric prospective study

Anna Elisabetta Vaudano, Alice Ballerini, Francesca Zucchini, Elisa Micalizzi, Simona Scolastico, Francesca Talami, Giada Giovannini, Matteo Pugnaghi, Niccolò Orlandi, Niccolò Biagioli, Maria Cristina Cioclu, Stefano Vallone, Maurilio Genovese, Alessandra Todeschini, Francesca Cavalleri, Marcella Malagoli, Stefano Meletti

doi : 10.1002/epd2.20050

To evaluate in a real clinical scenario the impact of the ILAE-recommended “Harmonized neuroimaging of epilepsy structural sequences�- HARNESS protocol in patients affected by focal epilepsy.

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Semiology characteristics and location of epileptogenic zone in motor seizures of axial and shoulder girdle muscles assessed by video stereoelectroencephalography study in 65 patients

Zhang Liping, Wang Jing, Yang Yujiao, Deng Qinqin, Yan Zhaofen, Liu Xinshan, Zhang Shidan, Zhou Jian, Guan Yuguang, Liu Changqing, Luan Guoming, Wang Mengyang

doi : 10.1002/epd2.20054

To study the semiology characteristics of motor seizures of axial and shoulder girdle muscles (ASMs) by stereoelectroencephalography (SEEG) and its value in determining location of epileptogenic zone.

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Cognitive impairment as a comorbidity of epilepsy in older adults: Analysis of global and domain-specific cognition

Xinyi Chai, Zhenxu Xiao, Qianhua Zhao, Jianhong Wang, Ding Ding, Jun Zhang

doi : 10.1002/epd2.20057

This study aimed to explore the association between epilepsy and cognitive impairment and to determine the factors associated with cognitive impairment in older people with epilepsy.

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Highly purified cannabidiol improves stability and postural tone in adult patients with Lennox–Gastaut syndrome: A case series

Carmen Calvello, Mariana Fernandes, Clementina Lupo, Fabio Placidi, Francesca Izzi, Ciro Bianco, Maria Grazia Celeste, Nicola Biagio Mercuri, Claudio Liguori

doi : 10.1002/epd2.20049

Lennox–Gastaut syndrome (LGS) is a severe developmental epileptic encephalopathy associated with numerous neurological signs and symptoms. Altered postural tone and the need for a caregiver-assisted wheelchair are features characterizing patients with LGS. Highly purified cannabidiol (CBD) is a novel antiseizure medication (ASM) recommended for seizure treatment, in combination with clobazam, in patients with LGS.

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Clinical and electroencephalographic findings prior to the onset of juvenile myoclonic epilepsy: A case series

Akiko Hiraiwa, Yu Kobayashi, Moemi Hojo, Jun Tohyama

doi : 10.1002/epd2.20052

The purpose of this study was to investigate the timing of generalized electroencephalographic abnormalities in patients with juvenile myoclonic epilepsy who were followed up long term before the onset of juvenile myoclonic epilepsy.

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Pregnancy and refractory epilepsy in Sturge–Weber syndrome: Challenges and outcomes

Jennifer Olson, Heather McKee

doi : 10.1002/epd2.20058

Sturge–Weber Syndrome (SWS) is a rare neurocutaneous disorder caused by focal vascular dysplasia. It is associated with facial angiomas, ocular abnormalities, epilepsy, intellectual disability, and leptomeningeal angiomas.

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Neurocysticercosis and epilepsy: Imaging and clinical characteristics

Ildefonso Rodríguez-Leyva, Karla Cantú-Flores, Arturo Domínguez-Frausto, Anna Elisabetta Vaudano, John Archer, Boris Bernhardt, Lorenzo Caciagli, Fernando Cendes, Yotin Chinvarun, Paolo Federico, William D. Gaillard, Eliane Kobayashi, Godwin Ogbole, Stefan Rampp, Irene Wang, Shuang Wang, Luis Concha

doi : 10.1002/epd2.20060

The ILAE Neuroimaging Task Force aimed to publish educational case reports highlighting basic aspects related to neuroimaging in epilepsy consistent with the educational mission of the ILAE.

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Association of ictal aphasia with hypoperfusion in language areas in temporal lobe epilepsy patients

Andrés Damian, Mariana Legnani, Patricia Braga, Rodolfo Ferrando

doi : 10.1002/epd2.20061

Ictal clinical phenomenology, including aphasia, is usually associated with increased regional cerebral perfusion. We present an unusual pattern of ictal cerebral perfusion in three patients with pharmacoresistant, lesional temporal lobe epilepsy and ictal/postictal aphasia studied with prolonged video-EEG, ictal, and interictal SPECT and MRI for pre-surgical evaluation.

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A super-elderly autopsy case of benign adult familial myoclonus epilepsy with a heterozygous mutation

Maya Tojima, Katsuya Kobayashi, Takefumi Hitomi, Haruka Ishibashi, Daisuke Yoshii, Makoto Sainouchi, Takashi Ayaki, Akihiro Shimotake, Kiyohide Usami, Takakuni Maki, Akiyoshi Kakita, Ryosuke Takahashi, Akio Ikeda

doi : 10.1002/epd2.20043

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Three consecutive epilepsy syndromes in one child

Min Jung Kim, Linda Huh, Anita N. Datta

doi : 10.1002/epd2.20051

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Progressive basal ganglia damage and EE-SWAS in a patient with a VPS13D pathogenic variant

Douglas R. Nordli III, Fernando N. Galan

doi : 10.1002/epd2.20031

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Sawtooth waves: An EEG normal variant

Fábio A. Nascimento, Sándor Beniczky

doi : 10.1002/epd2.20032

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