Zobrazeno 1 - 10
of 26
pro vyhledávání: '"Generalized myoclonic seizures"'
Autor:
Mateus Cardin Marquezani
Publikováno v:
Journal of Clinical Anesthesia and Pain Management. 5
Medication errorsare still one of the contributing factors leading to morbidity and mortality in anesthesia, despite measures to ensure patient safety. A 14-year-old male inadvertently received intrathecal tranexamic acid instead of hyperbaric bupiva
Publikováno v:
Epilepsy research. 170
Background A post-marketing surveillance study is investigating the safety and effectiveness of stiripentol during real-world clinical use in Japanese patients with Dravet syndrome (DS). Methods The safety and effectiveness of stiripentol were prospe
Publikováno v:
Journal of Epileptology, Vol 23, Iss 1, Pp 25-37 (2015)
SUMMARY Introduction. The traditional view of cognition in idiopathic or genetic generalized epilepsy (GGE) is that “one size fits all” i.e. only very mild generalized impairment might be detected, if any. This paper describes four case studies o
Autor:
Octavian V. Lie, L. Mukundan, Alexander M. Papanastassiou, Charles Ákos Szabó, Lola Morgan, Linda D. Leary
Publikováno v:
Epilepsy & Behavior Case Reports
Epilepsy and Behavior Case Reports, Vol 3, Iss C, Pp 4-7 (2015)
Epilepsy and Behavior Case Reports, Vol 3, Iss C, Pp 4-7 (2015)
We evaluated the spatiotemporal distribution of photic driving (PDR), photoparoxysmal (PPR), and photoconvulsive (PCR) responses recorded by intracranial electrodes (ic-EEG) in a patient with generalized photosensitivity and right frontal lobe cortic
Autor:
Mohamad A. Mikati, Faysal Tabbara
Publikováno v:
Epileptic disorders : international epilepsy journal with videotape. 19(1)
A 17-year-old female, of consanguineous parents, presented with a history of seizures and cognitive decline since the age of 12 years. She had absence, focal dyscognitive, generalized myoclonic, and generalized tonic-clonic seizures, all of which wer
Autor:
Roberto Caraballo, Santiago Flesler, Sebastian Fortini, Carolina Vilte, María Constanza Pasteris, María Francisca Lopez Avaria
Publikováno v:
Epilepsia. 54:1605-1612
Summary Purpose Myoclonic epilepsy in infancy (MEI) is characterized by brief generalized myoclonic seizures associated with generalized spike-wave paroxysms without other seizure types occurring in the first 3 years of life in developmentally normal
Autor:
Pierre-Marie Preux, Hun Chamroeun, Pierre Huc, Michel Dumas, Chan Samleng, Mey Vannareth, Kimly Chea, Devender Bhalla, Daniel Gérard, Mireille Cayreyre, Sophal Oum
Publikováno v:
Epilepsia. 52:1382-1387
PURPOSE: To estimate the lifetime prevalence of epilepsy in Prey Veng province (Cambodia). METHODS: Door-to-door screening was performed using a random cluster survey whereby all people >1 year of age were screened for epilepsy by using a validated a
Autor:
Gaetan Lesca, Julitta de Bellescize, Laurent Villard, Nathalie André-Obadia, Dorothée Ville, Anne-Lise Poulat, Mathieu Milh, Pierre Cacciagli
Publikováno v:
Epilepsy Research
Epilepsy Research, Elsevier, 2015, 111, pp.72-77. ⟨10.1016/j.eplepsyres.2015.01.008⟩
Epilepsy Research, 2015, 111, pp.72-77. ⟨10.1016/j.eplepsyres.2015.01.008⟩
Epilepsy Research, Elsevier, 2015, 111, pp.72-77. ⟨10.1016/j.eplepsyres.2015.01.008⟩
Epilepsy Research, 2015, 111, pp.72-77. ⟨10.1016/j.eplepsyres.2015.01.008⟩
International audience; Mutations in the TBC1D24 gene were first reported in an Italian family with a unique epileptic phenotype consisting of drug-responsive, early-onset idiopathic myoclonic seizures. Patients presented with isolated bilateral or f
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bf70c6c0cd2248ec3b822e8cb38a75c0
https://hal-amu.archives-ouvertes.fr/hal-01664298/document
https://hal-amu.archives-ouvertes.fr/hal-01664298/document
Autor:
Louis Vallée, Jullita De Bellecize, Nathalie Villeneuve, Hervé Isnard, Marie-Dominique Lamblin, Jacques Motte, Nicole Badinand, Stéphane Auvin, Florence Pandit
Publikováno v:
Epilepsia. 47:387-393
Summary: Purpose: Benign myoclonic epilepsy in infants (BMEI) is a rare epileptic syndrome characterized only by generalized myoclonic seizures (MSs) in normal children during the first 2 years. Our aim was to assess the electroclinical features and
Publikováno v:
Braindevelopment. 35(8)
Purpose The semiology of infantile seizures often shows different characteristics from that of adults. We performed this study to describe clinical and ictal characteristics of infantile seizures at less than two years of age. Methods A retrospective