Zobrazeno 1 - 10
of 227
pro vyhledávání: '"Severe epilepsy"'
Autor:
Michael S Salman, Sydney Martin
Publikováno v:
Journal of Multidisciplinary Healthcare
While ataxia is a relatively common presenting feature in pediatric patients, it represents only one possible cause of uncoordinated movements. Other possible causes of uncoordinated movements include ingestion of toxic substances, musculoskeletal di
Publikováno v:
Seizure. 91:425-436
Epilepsy is a common, often severe, feature of LAMA2-related muscular dystrophy (LAMA2-RD) and could represent its onset and main manifestation, even in the absence of overt muscle involvement. To date, there is no systematic characterization of epil
Autor:
Jaqueline C Geraldis, Estela M. Bruxel, Danielle do Carmo Ferreira Bruno, Alexandre B Godoi, Mariana Martin, Amanda Morato do Canto, Iscia Lopes-Cendes
Publikováno v:
Seizure. 90:34-50
Mesial temporal lobe epilepsy (MTLE) is one of the most common types of focal epilepsy in the adult population. MTLE is frequently associated with a specific histopathological lesion in the medial temporal structures, namely hippocampal sclerosis (HS
Autor:
Abigail Van Nuland, Mary Anne Meskis, Nicole Villas, Anne T. Berg, Anna Ivanenko, Kelly G. Knupp
Publikováno v:
Seizure. 85:102-110
Objectives To describe and quantify the nature and severity of sleep disruptions in young people with Dravet syndrome (DS) based upon parent report. Methods Qualitative review of available pediatric sleep instruments with parent members of the Dravet
Autor:
Michelle A. Farrar, D. Flanagan, Vanessa Sarkozy, John A. Lawson, Clara W. T. Chung, David Mowat, Sean E. Kennedy, Denise L Chan
Publikováno v:
Pediatric Research. 89:1447-1451
Background Literature regarding congenital subependymal giant cell astrocytomas (SEGA) is limited, and suggests they are at risk of rapid growth and complications. We sought to characterise the growth patterns of congenital SEGA. The second part of t
Autor:
Ethan M. Goldberg
Publikováno v:
Epilepsy Currents
Annals of Neurology
Annals of Neurology
dCas9-Based Scn1a Gene Activation Restores Inhibitory Interneuron Excitability and Attenuates Seizures in Dravet Syndrome MiceColasante G, Lignani G, Brusco S, et al. Mol Ther. 2020;28(1):235-253. doi:10.1016/j.ymthe.2019.08.018Dravet syndrome (DS) i
Autor:
Tuba Kurt, Elif Çoban, Süleyman Caner Karahan, Ali Cansu, Elif Acar Arslan, Sevim Şahin, Tülay Kamaşak, Betül Diler Durgut, Beril Dilber, Serap Ozer Yaman
Publikováno v:
Epileptic Disorders. 22:183-193
The purpose of this study was to compare HMGB-1, TLR4, IL-1β, IL-1R1, and TNF-α levels in patients with mild and severe epilepsy with those in a healthy control group. Children aged 4-17 years, diagnosed with epilepsy for at least three years and w
Autor:
Pasquale Striano, Mariagrazia Esposito, Alice Bonuccelli, Diego Peroni, Alessandro Orsini, Ilaria Lagorio
Publikováno v:
Expert Review of Precision Medicine and Drug Development. 5:101-108
Introduction: The large number of different syndromes and seizure types, together with an inter-individual variable response to antiepileptic drugs (AEDs), makes the treatment of epilepsy c...
Autor:
Roberta Solazzi, Francesca Ragona, Tiziana Granata, Jacopo C. DiFrancesco, Stefano D'Arrigo, Stefania Magri, Giuliana Messina, Barbara Castellotti, Elena Freri, Cinzia Gellera, Chiara Vannicola, Laura Canafoglia
Publikováno v:
Seizure. 88:143-145