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@ARTICLE{Leonide:10137,
author = {Leonide, A. and Rüger, B. and Weber, A. and Meulenberg, W.
A. and Ivers-Tiffée, E.},
title = {{I}mpedance {S}tudy of {A}lternative
({L}a,{S}r){F}e{O}3-and ({L}a,{S}r)({C}o,{F}e){O}3- {MIEC}
{C}athode {C}ompositions},
journal = {Journal of the Electrochemical Society},
volume = {157},
issn = {0013-4651},
address = {Pennington, NJ},
publisher = {Electrochemical Society},
reportid = {PreJuSER-10137},
pages = {B234 - B239},
year = {2010},
note = {Funding by the Fuel Cell Research Alliance
Baden-Wurttemberg (project 23-729.90 5/371) is gratefully
acknowledged.},
abstract = {This open-label extension evaluated the long-term efficacy
and tolerability of rufinamide in patients with
Lennox-Gastaut syndrome (LGS) who had previously completed a
12-week double-blind study.In total, 124 patients (aged 4-37
years), receiving 1-3 concomitant antiepileptic drugs, were
treated with rufinamide approximately 25-60 mg/kg/day.
Efficacy was assessed by seizure frequency; tolerability by
adverse events (AEs) and laboratory tests.Overall, patients
were treated with rufinamide for a median (range) of 432
(10-1149) days. Reductions in seizure frequency were
observed throughout the study; during the last 12 months of
treatment, $41.0\%$ and $47.9\%$ of patients had > or =
$50\%$ reduction in total and tonic-atonic seizure
frequency, respectively. The most common AEs were vomiting
$(30.6\%)$ and pyrexia $(25.8\%).In$ this open-label
extension, rufinamide appeared to be an effective long-term
adjunctive therapy for the treatment of LGS-associated
seizures in children and young adults.},
cin = {IEF-1},
ddc = {540},
cid = {I:(DE-Juel1)VDB809},
pnm = {Rationelle Energieumwandlung},
pid = {G:(DE-Juel1)FUEK402},
shelfmark = {Electrochemistry / Materials Science, Coatings $\&$ Films},
typ = {PUB:(DE-HGF)16},
UT = {WOS:000273222700026},
doi = {10.1149/1.3265473},
url = {https://juser.fz-juelich.de/record/10137},
}