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pro vyhledávání: '"E, Andermann"'
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Akademický článek
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Autor:
Dina Amrom, Samuel F. Berkovic, Frederick Andermann, Amit Bar-Or, Y. M. Hart, Demet Kinay, Ken Laxer, E. Andermann
Publikováno v:
Neurology. 83:1049-1055
Objective: To describe a potential association between comorbid autoimmune disease and Rasmussen encephalitis (RE) and discuss potential insights into underlying RE pathogenesis. Methods: We report a case series of 4 patients with RE in whom a comorb
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fc700428c74fa11945a88b565ca89a6f
https://doi.org/10.1212/wnl.0000000000000791
https://doi.org/10.1212/wnl.0000000000000791
Publikováno v:
Neurology. 70:607-616
Background: Currently, there are no published randomized controlled trials evaluating the efficacy and safety of adjunctive antiepileptic therapy in idiopathic generalized epilepsy with myoclonic seizures. Methods: This randomized, double-blind, plac
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7107570158d8929d31825d4cffc6b9cd
https://doi.org/10.1212/01.wnl.0000297512.18364.40
https://doi.org/10.1212/01.wnl.0000297512.18364.40
Autor:
Neda Bernasconi, François Dubeau, Li M. Li, Andrea Bernasconi, C.A.M. Guerreiro, Fernando Cendes, D. Kinay, Maria Augusta Montenegro, F. Andermann, Ana Carolina Coan, Iscia Lopes-Cendes, M M Guerreiro, E. Andermann
Publikováno v:
Journal of Neurology, Neurosurgery & Psychiatry. 77:367-371
Objective: To assess whether different types of malformation of cortical development (MCD) are associated with specific patterns of hippocampal abnormalities. Methods: A total of 122 consecutive patients with MRI diagnosis of MCD (53 males, age range
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2db2742ee826d7d33bb8c88670c8714f
https://doi.org/10.1136/jnnp.2005.070417
https://doi.org/10.1136/jnnp.2005.070417
Autor:
François Dubeau, A. Bastos, F. Andermann, Hiroshi Otsubo, André Olivier, André Palmini, Marilisa M. Guerreiro, Paul A. Hwang, H. J. Hoffman, G. J. Snipes, E. Andermann, Theodore Rasmussen
Publikováno v:
Neurology. 51:1263-1269
Background: Seizures in patients with tuberous sclerosis complex (TSC) are often intractable to antiepileptic medications and searching investigation may provide evidence that surgical treatment can be considered. Objective: To review the results of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4ddb60977b560269598243d5905077b3
https://doi.org/10.1212/wnl.51.5.1263
https://doi.org/10.1212/wnl.51.5.1263
Publikováno v:
ResearcherID
We describe the clinical characteristics of a group of patients with familial temporal lobe epilepsy (TLE) in 11 kindreds with 36 affected individuals identified and investigated at the Montreal Neurological Hospital. Seizure types were simple partia
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b412b3098d4ecba294924da238ab427e
https://doi.org/10.1212/wnl.50.2.554
https://doi.org/10.1212/wnl.50.2.554
Publikováno v:
Neurology. 46:766-772
Because hereditary hyperekplexia results from a defect in the glycine receptor, we studied in five patients several spinal inhibitory pathways that are thought to use either glycine or gamma-aminobutyric acid as a neurotransmitter. Three patients had
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4651f6e07f8231c3e00791a3a641a55e
https://doi.org/10.1212/wnl.46.3.766
https://doi.org/10.1212/wnl.46.3.766
Autor:
M, Cadieux-Dion, E, Andermann, P, Lachance-Touchette, O, Ansorge, C, Meloche, A, Barnabé, R I, Kuzniecky, F, Andermann, E, Faught, S, Leonberg, J A, Damiano, S F, Berkovic, G A, Rouleau, P, Cossette
Publikováno v:
Clinical genetics. 83(6)
We sought to identify the molecular basis of the autosomal dominant form of Kufs disease, an adult onset form of neuronal ceroid lipofuscinosis. We used a combination of classic linkage analysis and Next Generation Sequencing to map and identify muta
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::c15186f4ef03076520687fd8ae76a37c
https://pubmed.ncbi.nlm.nih.gov/22978711
https://pubmed.ncbi.nlm.nih.gov/22978711