Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Noelia Chamorro"'
Autor:
Thomas Czech, Galymzhan Issabekov, Yi Yao, Lily C. Wong-Kisiel, Valeria L. Muro, Faisal Al Otaibi, Anthony C. Wang, Chima O. Oluigbo, Noelia Chamorro, Xinkai Zhou, Howard L. Weiner, Christian Raftapoulos, Shao-Chun Li, Jeffrey Bolton, Maria Angeles Pérez-Jiménez, Jianguo Zhang, Martin N. Stienen, Martha Feucht, Mashael Al Khateeb, Josef Zentner, Jiu Luan Lin, Olivia Kola, Daniel Delev, Niklaus Krayenbühl, Chi-Hong Tseng, Evan Cole Lewis, Christian Dorfer, Poodipedi Sarat Chandra, Samuel Lapalme-Remis, Kai Zhang, Valentina Baro, Qiang Guo, Manjari Tripathi, Aria Fallah, Mary Connelly, Hongwei Zhu, Georgia Ramantani, Marcelo Budke, Jeffrey G. Ojemann, Brent R. O'Neill, Matthew D. Smyth, William D. Gaillard, Walter Hader, Marec von Lehe, Roy W. R. Dudley, Li Xin Cai, Pierre Olivier Champagne, Robert J. Bollo, Eveline Teresa Hidalgo, Kao Min Lin, Juan Pociecha, Silvia Vieker, Pauline Michel, Alexander G. Weil, Phillip L. Pearl, John Ragheb, Paul Steinbok, George M. Ibrahim, Karl Lothard Schaller, Wenjing Zhou, P. Finet, Christian Cantillano Malone, Gary W. Mathern, Feng Peng Wang, Qing Zhu Liu, Sanjiv Bhatia
Publikováno v:
Epilepsia, Vol. 62, no.5, p. 1064-1073 (2021)
Objective To develop and validate a model to predict seizure freedom in children undergoing cerebral hemispheric surgery for the treatment of drug-resistant epilepsy. Methods We analyzed 1267 hemispheric surgeries performed in pediatric participants
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::34f341e071f19ac00af74ca3f01e010f
https://doi.org/10.1111/epi.16861
https://doi.org/10.1111/epi.16861
Autor:
Marcelo Budke, Brent R. O'Neill, Lily C. Wong-Kisiel, Anthony C. Wang, Chima O. Oluigbo, Feng-Peng Wang, Daniel Delev, Chi-Hong Tseng, Poodipedi Sarat Chandra, Martha Feucht, Mary B. Connolly, Faisal Al Otaibi, Yi Yao, Manjari Tripathi, Olivia Kola, Noelia Chamorro, Martin N. Stienen, Jiuluan Lin, Walter Hader, John Ragheb, Valentina Baro, Qiang Guo, Aria Fallah, Georgia Ramantani, Jia-Shu Chen, Valeria L. Muro, Matthew D. Smyth, Qingzhu Liu, George M. Ibrahim, Galymzhan Issabekov, Eveline Teresa Hidalgo, Karl Lothard Schaller, William D. Gaillard, Wenjing Zhou, Evan J. H. Lewis, Maria Angeles Pérez-Jiménez, Roy W. R. Dudley, Alexander G. Weil, Tristan Brunette-Clément, Marec von Lehe, Jeffrey Bolton, Jianguo Zhang, William B. Harris, Sanjiv Bhatia, Christian Raftopoulos, Josef Zentner, Shao-Chun Li, Niklaus Krayenbühl, Lixin Cai, Christian Dorfer, Mashael Al-Khateeb, Pierre-Olivier Champagne, Kai Zhang, Thomas Czech, Robert J. Bollo, Silvia Vieker, Pauline Michel, Paul Steinbok, P. Finet, Christian Cantillano Malone, Gary W. Mathern, Howard L. Weiner, Hongwei Zhu, Samuel Lapalme-Remis, Juan Pociecha, Phillip L. Pearl, Kao-Min Lin
Publikováno v:
Epilepsia, vol 62, iss 11
Epilepsia, Vol. 62, no. 11, p. 2707-2718 (2021)
Epilepsia, Vol. 62, no. 11, p. 2707-2718 (2021)
ObjectiveThis study was undertaken to determine whether the vertical parasagittal approach or the lateral peri-insular/peri-Sylvian approach to hemispheric surgery is the superior technique in achieving long-term seizure freedom.MethodsWe conducted a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::da76549fdcfdedd01bd88ba911dedcad
https://escholarship.org/uc/item/6fc8k7s7
https://escholarship.org/uc/item/6fc8k7s7
Autor:
Lily C. Wong-Kisiel, Christian Raftapoulos, George M. Ibrahim, Anthony C. Wang, Chima O. Oluigbo, Paul Steinbok, Robert J. Bollo, Evan Cole Lewis, Silvia Vieker, Karl Lothard Schaller, Wenjing Zhou, Pauline Michel, Jiu-Luan Lin, Christian Dorfer, Hongwei Zhu, Pierre Olivier Champagne, Georgia Ramantani, Jeffrey Bolton, Martha Feucht, Marec von Lehe, Juan Pociecha, Phillip L. Pearl, Matthew D. Smyth, Kao-Min Lin, Feng-Peng Wang, Yi Yao, Manjari Tripathi, Walter Hader, Shao-Chun Li, Daniel Delev, Lixin Cai, Noelia Chamorro, Faisal Al Otaibi, Qiang Guo, Chi-Hong Tseng, John Ragheb, Niklaus Krayenbühl, Eveline Teresa Hidalgo, Josef Zentner, Aria Fallah, Maria Angeles Pérez-Jiménez, Martin N. Stienen, Marcelo Budke, Alexander G. Weil, Brent R. O'Neill, Qingzhu Liu, Kai Zhang, P. Sarat Chandra, Mashael Al Khateeb, Jeffrey G. Ojemann, Xinkai Zhou, William D. Gaillard, Roy W. R. Dudley, Sanjiv Bhatia, Jian-Guo Zhang, Valentina Baro, Howard L. Weiner, Galymzhan Issabekov, Thomas Czech, Valeria L. Muro, Samuel Lapalme-Remis, Olivia Kola, Mary Connelly, P. Finet, Christian Cantillano Malone, Gary W. Mathern
Publikováno v:
SSRN Electronic Journal.
Background: A subset of pediatric epilepsy patients suffer from epilepsy syndromes related to multi-lobar or hemispheric epileptogenic networks and diseases. Most of these patients are refractory to anti-seizure drug treatment, resulting in persisten
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b6512332b74f2d426894bf56255d6c2b
https://doi.org/10.2139/ssrn.3514748
https://doi.org/10.2139/ssrn.3514748
Publikováno v:
Archivos Argentinos de Pediatria. 117
Opsoclonus-myoclonus syndrome is a rare disorder among pediatric patients. The diagnosis is clinical and is characterized by the presence of at least three of the following: opsoclonus, myoclonus, ataxia, irritability and sleep disorders. In over 50
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::527f2b18f9a6099ce876a07a4b40dec8
https://doi.org/10.5546/aap.2019.e651
https://doi.org/10.5546/aap.2019.e651
Autor:
Gabriela, Urman, Maia, Leivi, Noelia, Chamorro, Brenda, García, Adrián, Callea, Arnoldo, Grosman
Publikováno v:
Archivos argentinos de pediatria. 117(6)
Opsoclonus-myoclonus syndrome is a rare disorder among pediatric patients. The diagnosis is clinical and is characterized by the presence of at least three of the following: opsoclonus, myoclonus, ataxia, irritability and sleep disorders. In over 50
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::73ceb8e4ca50abefc7d78a082300b940
https://pubmed.ncbi.nlm.nih.gov/31758904
https://pubmed.ncbi.nlm.nih.gov/31758904
Autor:
Roberto Caraballo, Pablo Sebastian Fortini, Ricardo Cersósimo, Belen Ramirez, Carolina Vilte, Noelia Chamorro
Publikováno v:
Journal of Pediatric Epilepsy. :173-180
We present an update of a series of patients with myoclonic status in non-progressive encephalopaties (MSNPE) describing the electroclinical features and outcome. Between February 1, 1990 and June 30, 2011, 41 patients who met diagnostic criteria of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b05c98e8677020c55b677f8f02f349a0
https://doi.org/10.3233/pep-14088
https://doi.org/10.3233/pep-14088
Autor:
Noelia Chamorro, María C. Kaltenmeier, Ana María Soprano, Natalia Cejas, Sebastian Fortini, Roberto Caraballo
Publikováno v:
Seizure. 23(2):98-104
Purpose The aim of the study was to retrospectively analyze the electroclinical features, etiology, treatment, and prognosis of 29 patients with Landau–Kleffner syndrome (LKS) with a long-term follow-up. Methods Inclusion criteria were a diagnosis
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dfc28b51b8d32f0b228e112dbefad037
Publikováno v:
Pediatric Neurology. 48:355-362
Epilepsy with myoclonic-atonic seizures is characterized by myoclonic-atonic, absence, tonic-clonic, and eventually tonic seizures, appearing in previously normal children at ages 18-60 months. We analyzed the electroclinical features, treatment, and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ce4bfeb6ac31be11a3c547128bc3a2a3
https://doi.org/10.1016/j.pediatrneurol.2012.12.022
https://doi.org/10.1016/j.pediatrneurol.2012.12.022