Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Robert S, Delamont"'
Publikováno v:
Sultan Qaboos University Medical Journal, Vol 14, Iss 4, Pp 473-477 (2014)
Objectives: The aim of this study was to establish the relationship between background amplitude and interictal abnormalities in routine electroencephalography (EEG). Methods: This retrospective audit was conducted between July 2006 and December 2009
Externí odkaz:
https://doaj.org/article/313a80e22e314977bb458ffb496e0a78
Autor:
Matthew C. Walker, Robert S. Delamont
Publikováno v:
Epilepsy Research. 97:267-272
Summary Autonomic measures frequently alter with seizure activity and with brain state and so theoretically, there could be pre-ictal changes in autonomic function. However, there are considerable confounders. First, the measurement of autonomic func
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3bc6e1a486d89fd2d7d1daba5cf9e23f
https://doi.org/10.1016/j.eplepsyres.2011.10.016
https://doi.org/10.1016/j.eplepsyres.2011.10.016
Publikováno v:
Epilepsia. 57
The risk of dying suddenly and unexpectedly is increased 24- to 28-fold among young people with epilepsy compared to the general population, but the incidence of sudden unexpected death in epilepsy (SUDEP) varies markedly depending on the epilepsy po
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3462b2ad16a733b74a70ae506c795cdf
https://pubmed.ncbi.nlm.nih.gov/26749012
https://pubmed.ncbi.nlm.nih.gov/26749012
Publikováno v:
Clinical Neurophysiology. 124:1258-1260
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3179e88d925be8de6a0da0153c5b9305
https://doi.org/10.1016/j.clinph.2012.10.016
https://doi.org/10.1016/j.clinph.2012.10.016
Autor:
Peter O.O. Julu, Giorgio Pini, Eric Smeets, Robert S. Delamont, Flora Apartopoulos, Ingegerd Witt Engerström, Stig Hansen, Bengt Engerström
Publikováno v:
The Lancet. 371:1981-1983
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8fde1cf685df33093ba118aa26b57452
https://doi.org/10.1016/s0140-6736(08)60849-1
https://doi.org/10.1016/s0140-6736(08)60849-1
Autor:
Giorgio, Pini, Stefania, Bigoni, Ingegerd Witt, Engerström, Olga, Calabrese, Beatrice, Felloni, Maria Flora, Scusa, Pietro, Di Marco, Paolo, Borelli, Ubaldo, Bonuccelli, Peter O O, Julu, Jytte Bieber, Nielsen, Bodil, Morin, Stig, Hansen, Giuseppe, Gobbi, Paola, Visconti, Maria, Pintaudi, Veneselli, Edvige, Anna, Romanelli, Fabrizio, Bianchi, Manuela, Casarano, Roberta, Battini, Giovanni, Cioni, Francesca, Ariani, Alessandra, Renieri, Alberto, Benincasa, Robert S, Delamont, Michele, Zappella, Eric E J, Smeets
Publikováno v:
Neuropediatrics, 43(1), 37-43. Georg Thieme Verlag
Rett syndrome (RTT) is a severe neurodevelopmental disorder affecting almost exclusively females. The Hanefeld variant, or early-onset seizure variant, has been associated with mutations in CDKL5 gene.In recent years more than 60 patients with mutati
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a0409f97ebac9c4fbd6e76388ad1f213
http://hdl.handle.net/11568/202217
http://hdl.handle.net/11568/202217
