This HTML5 document contains 58 embedded RDF statements represented using HTML+Microdata notation.

The embedded RDF content will be recognized by any processor of HTML5 Microdata.

Namespace Prefixes

PrefixIRI
dctermshttp://purl.org/dc/terms/
n15http://linked.opendata.cz/resource/domain/vavai/riv/tvurce/
n5http://linked.opendata.cz/ontology/domain/vavai/
n8http://linked.opendata.cz/resource/domain/vavai/zamer/
shttp://schema.org/
skoshttp://www.w3.org/2004/02/skos/core#
n3http://linked.opendata.cz/ontology/domain/vavai/riv/
n2http://linked.opendata.cz/resource/domain/vavai/vysledek/
n10http://linked.opendata.cz/resource/domain/vavai/vysledek/RIV%2F00064203%3A_____%2F10%3A6053%21RIV11-MZ0-00064203/
rdfhttp://www.w3.org/1999/02/22-rdf-syntax-ns#
n4http://linked.opendata.cz/ontology/domain/vavai/riv/klicoveSlovo/
n16http://linked.opendata.cz/ontology/domain/vavai/riv/duvernostUdaju/
xsdhhttp://www.w3.org/2001/XMLSchema#
n14http://linked.opendata.cz/ontology/domain/vavai/riv/aktivita/
n12http://linked.opendata.cz/ontology/domain/vavai/riv/jazykVysledku/
n17http://linked.opendata.cz/ontology/domain/vavai/riv/obor/
n11http://linked.opendata.cz/ontology/domain/vavai/riv/druhVysledku/
n6http://reference.data.gov.uk/id/gregorian-year/

Statements

Subject Item
n2:RIV%2F00064203%3A_____%2F10%3A6053%21RIV11-MZ0-00064203
rdf:type
n5:Vysledek skos:Concept
dcterms:description
Purpose: Anecdotal reports have described cortical malformations in epileptic patients with Sturge-Weber syndrome (SWS). No data are available regarding the prevalence and significance of this association. Methods: We reviewed retrospectively the clinical profile, preoperative magnetic resonance imaging (MRI) studies, and pathology reports of all patients with SWS and medically intractable epilepsy evaluated in our epilepsy surgery program between 1979 and 2006. Results: Twelve patients (male/female = 7/5) were identified. Mean age at seizure onset was 11.1 +/- 16.7 months. Seizures occurred daily in seven patients and weekly in five patients. A facial port-wine stain was noted in 10 cases. Eleven patients evidenced developmental delay and eight were hemiparetic. Eight patients underwent excisional surgery for epilepsy (mean age 10.3 +/- 6.5 year), including hemispherectomy (n = 4) and focal cortical resection (n = 4). Purpose: Anecdotal reports have described cortical malformations in epileptic patients with Sturge-Weber syndrome (SWS). No data are available regarding the prevalence and significance of this association. Methods: We reviewed retrospectively the clinical profile, preoperative magnetic resonance imaging (MRI) studies, and pathology reports of all patients with SWS and medically intractable epilepsy evaluated in our epilepsy surgery program between 1979 and 2006. Results: Twelve patients (male/female = 7/5) were identified. Mean age at seizure onset was 11.1 +/- 16.7 months. Seizures occurred daily in seven patients and weekly in five patients. A facial port-wine stain was noted in 10 cases. Eleven patients evidenced developmental delay and eight were hemiparetic. Eight patients underwent excisional surgery for epilepsy (mean age 10.3 +/- 6.5 year), including hemispherectomy (n = 4) and focal cortical resection (n = 4).
dcterms:title
Medically intractable epilepsy in Sturge-Weber syndrome is associated with cortical malformation: Implications for surgical therapy Medically intractable epilepsy in Sturge-Weber syndrome is associated with cortical malformation: Implications for surgical therapy
skos:prefLabel
Medically intractable epilepsy in Sturge-Weber syndrome is associated with cortical malformation: Implications for surgical therapy Medically intractable epilepsy in Sturge-Weber syndrome is associated with cortical malformation: Implications for surgical therapy
skos:notation
RIV/00064203:_____/10:6053!RIV11-MZ0-00064203
n3:aktivita
n14:I n14:Z
n3:aktivity
I, Z(MZ0FNM2005)
n3:cisloPeriodika
2
n3:dodaniDat
n6:2011
n3:domaciTvurceVysledku
n15:9525300
n3:druhVysledku
n11:J
n3:duvernostUdaju
n16:S
n3:entitaPredkladatele
n10:predkladatel
n3:idSjednocenehoVysledku
270264
n3:idVysledku
RIV/00064203:_____/10:6053
n3:jazykVysledku
n12:eng
n3:klicovaSlova
Sturge-Weber syndrome; Epilepsy; Young children; Polymicrogyria; Cortical dysplasia; pediatric epilepsy; fdg-pet; children; disease; abnormalities; dysplasia; migration; perfusion; surgery; mri
n3:klicoveSlovo
n4:mri n4:fdg-pet n4:Polymicrogyria n4:children n4:pediatric%20epilepsy n4:perfusion n4:surgery n4:disease n4:Young%20children n4:abnormalities n4:Cortical%20dysplasia n4:Epilepsy n4:migration n4:dysplasia n4:Sturge-Weber%20syndrome
n3:kodStatuVydavatele
US - Spojené státy americké
n3:kontrolniKodProRIV
[6429042D55E5]
n3:nazevZdroje
Epilepsia
n3:obor
n17:FH
n3:pocetDomacichTvurcuVysledku
1
n3:pocetTvurcuVysledku
9
n3:rokUplatneniVysledku
n6:2010
n3:svazekPeriodika
51
n3:tvurceVysledku
Ragheb, J. Castellano-Sanchez, A. Jayakar, P. Koehn, M. Resnick, T. Morrison, G. Duchowny, M. Kršek, Pavel Maton, B.
n3:wos
000274144900010
n3:zamer
n8:MZ0FNM2005
s:issn
0013-9580
s:numberOfPages
11