Zobrazeno 1 - 10
of 32
pro vyhledávání: '"Barbora, Benova"'
Autor:
Hanna M. Hulshof, Barbora Benova, Pavel Krsek, Martin Kyncl, Maarten H. Lequin, Anezka Belohlavkova, Petr Jezdik, Kees P. J. Braun, Floor E. Jansen
Publikováno v:
Epilepsia Open, Vol 6, Iss 4, Pp 663-671 (2021)
Abstract Objective Patients with tuberous sclerosis complex (TSC) present with drug‐resistant epilepsy in about 60% of cases, and evaluation for epilepsy surgery may be warranted. Correct delineation of the epileptogenic zone (EZ) among multiple dy
Externí odkaz:
https://doaj.org/article/9b8a42fcea844aa685ea68c71fae0e56
Autor:
Jessie De Ridder, Mario Lavanga, Birgit Verhelle, Jan Vervisch, Katrien Lemmens, Katarzyna Kotulska, Romina Moavero, Paolo Curatolo, Bernhard Weschke, Kate Riney, Martha Feucht, Pavel Krsek, Rima Nabbout, Anna C. Jansen, Konrad Wojdan, Dorota Domanska-Pakieła, Magdalena Kaczorowska-Frontczak, Christoph Hertzberg, Cyrille H. Ferrier, Sharon Samueli, Barbora Benova, Eleonora Aronica, David J. Kwiatkowski, Floor E. Jansen, Sergiusz Jóźwiak, Sabine Van Huffel, Lieven Lagae
Publikováno v:
Frontiers in Neurology, Vol 11 (2020)
Tuberous Sclerosis Complex (TSC) is a multisystem genetic disorder with a high risk of early-onset epilepsy and a high prevalence of neurodevelopmental comorbidities, including intellectual disability and autism spectrum disorder (ASD). Therefore, TS
Externí odkaz:
https://doaj.org/article/5e5b31c5c880467a8726961a4a17973e
Autor:
Sophie Adler, Sara Lorio, Thomas S. Jacques, Barbora Benova, Roxana Gunny, J. Helen Cross, Torsten Baldeweg, David W. Carmichael
Publikováno v:
NeuroImage: Clinical, Vol 15, Iss , Pp 95-105 (2017)
Focal cortical dysplasias (FCDs) are a range of malformations of cortical development each with specific histopathological features. Conventional radiological assessment of standard structural MRI is useful for the localization of lesions but is unab
Externí odkaz:
https://doaj.org/article/76b71ddf474b4e4aac3662d4534d4f42
Autor:
Barbora Benova, Anezka Belohlavkova, Petr Jezdik, Alena Jahodová, Martin Kudr, Vladimir Komarek, Vilem Novak, Petr Liby, Robert Lesko, Michal Tichý, Martin Kyncl, Josef Zamecnik, Pavel Krsek, Alice Maulisova
Publikováno v:
PeerJ, Vol 7, p e7790 (2019)
Background We aimed first to describe trends in cognitive performance over time in a large patient cohort (n = 203) from a single tertiary centre for paediatric epilepsy surgery over the period of 16 years divided in two (developing—pre-2011 vs. es
Externí odkaz:
https://doaj.org/article/48f351d87a3b424b9c7f82e23ae94af6
Autor:
Petr Jezdik, Maarten H. Lequin, Floor E. Jansen, Barbora Benova, Martin Kyncl, Hanna M. Hulshof, Kees P.J. Braun, Anezka Belohlavkova, Pavel Krsek
Publikováno v:
Epilepsia Open, Vol 6, Iss 4, Pp 663-671 (2021)
Objective Patients with tuberous sclerosis complex (TSC) present with drug‐resistant epilepsy in about 60% of cases, and evaluation for epilepsy surgery may be warranted. Correct delineation of the epileptogenic zone (EZ) among multiple dysplastic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dce0b606dc873aff7e162ef76cf22145
https://doaj.org/article/9b8a42fcea844aa685ea68c71fae0e56
https://doaj.org/article/9b8a42fcea844aa685ea68c71fae0e56
Autor:
Petr Liby, Alena Jahodova, Barbora Benova, Radek Janca, Martin Kyncl, Pavel Krsek, Petr Jezdik, Martin Kudr, Anezka Belohlavkova, Michal Tichy, Jakub Taborsky, Matyas Ebel
Publikováno v:
European Journal of Paediatric Neurology. 35:49-55
Object Epilepsy surgery is an effective treatment for selected patients with focal intractable epilepsy. Complete removal of the epileptogenic zone significantly increases the chances for postoperative seizure-freedom. In complex surgical candidates,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ba1a59ff95fbeb66f3db73dbae3dfa7d
https://doi.org/10.1016/j.ejpn.2021.09.012
https://doi.org/10.1016/j.ejpn.2021.09.012
Autor:
Eleonora Aronica, Maurits W.C.B. Sanders, Barbora Benova, Kees P.J. Braun, Vilém Novák, Anezka Belohlavkova, Anna Uhrova-Meszarosova, Barbora Hermanovska, Bobby P. C. Koeleman, Marketa Vlckova, David Stanek, Floor E. Jansen, Josef Zamecnik, Pavel Krsek
Publikováno v:
European journal of paediatric neurology : EJPN, 30, 88-96. W.B. Saunders Ltd
Background Variants of GATOR1-genes represent a recognised cause of focal cortical dysplasia (FCD), the most common structural aetiology in paediatric drug-resistant focal epilepsy. Reports on familial cases of GATOR1-associated FCD are limited, espe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a145929a3102b09f8e4571f34275e582
https://doi.org/10.1016/j.ejpn.2020.12.001
https://doi.org/10.1016/j.ejpn.2020.12.001
Autor:
Carmen, Barba, Ingmar, Blumcke, Melodie R, Winawer, Till, Hartlieb, Hoon-Chul, Kang, Laura, Grisotto, Mathilde, Chipaux, Christian G, Bien, Barbora, Heřmanovská, Brenda E, Porter, Hart G W, Lidov, Valentina, Cetica, Friedrich G, Woermann, Javier A, Lopez-Rivera, Peter D, Canoll, Irina, Mader, Ludovico, D'Incerti, Sara, Baldassari, Edward, Yang, Ahmed, Gaballa, Hannes, Vogel, Barbora, Benova, Letizia, Macconi, Tilman, Polster, Gerald A, Grant, Lenka, Krsková, Hui Jin, Shin, Ara, Ko, Peter B, Crino, Pavel, Krsek, Jeong Ho, Lee, Dennis, Lal, Stéphanie, Baulac, Annapurna, Poduri, Renzo, Guerrini
Publikováno v:
Neurology
BACKGROUND AND OBJECTIVES: The SLC35A2 gene, located at chromosome Xp11.23, encodes for a uridine diphosphate–galactose transporter. We describe clinical, genetic, neuroimaging, EEG, and histopathologic findings and assess possible predictors of po
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::82371b127438734bbafca5bc470cae5d
https://pubmed.ncbi.nlm.nih.gov/36307217
https://pubmed.ncbi.nlm.nih.gov/36307217
Autor:
Angelika Mühlebner, Jackelien van Scheppingen, Hanna M Hulshof, Theresa Scholl, Anand M Iyer, Jasper J Anink, Ans M W van den Ouweland, Mark D Nellist, Floor E Jansen, Wim G M Spliet, Pavel Krsek, Barbora Benova, Josef Zamecnik, Peter B Crino, Daniela Prayer, Thomas Czech, Adelheid Wöhrer, Jasmin Rahimi, Romana Höftberger, Johannes A Hainfellner, Martha Feucht, Eleonora Aronica
Publikováno v:
PLoS ONE, Vol 11, Iss 6, p e0157396 (2016)
Tuberous Sclerosis Complex (TSC) is a genetic hamartoma syndrome frequently associated with severe intractable epilepsy. In some TSC patients epilepsy surgery is a promising treatment option provided that the epileptogenic zone can be precisely delin
Externí odkaz:
https://doaj.org/article/3b4361f6c3404a0ab17dc4ed6bddecb7
Autor:
Barbora Benova, Robert Lesko, Martin Kudr, Petr Jezdik, Michal Tichy, Petr Liby, Josef Zamecnik, Alena Jahodova, Pavel Krsek
Publikováno v:
Journal of Neurosurgery: Pediatrics. 26:533-542
OBJECTIVEIn this study, the authors aimed to determine 1) whether the use of intraoperative electrocorticography (ECoG) affects outcomes and complication rates of children undergoing resective epilepsy surgery; 2) which patient- and epilepsy-related
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::85efefeb3fb66f307309b7b09b7eca25
https://doi.org/10.3171/2020.4.peds20198
https://doi.org/10.3171/2020.4.peds20198