Source:http://linkedlifedata.com/resource/pubmed/id/21557146
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
1
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pubmed:dateCreated |
2011-5-10
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pubmed:abstractText |
Epilepsy with myoclonic absences (EMA) is a rare epileptic syndrome with frequently poor response to antiepileptic treatment. Rufinamide (RUF) is a relatively new EMEA- and FDA-approved anticonvulsant licensed as an orphan drug for the adjunctive treatment of patients with Lennox-Gastaut syndrome.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:month |
Feb
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pubmed:issn |
1439-1899
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pubmed:author | |
pubmed:copyrightInfo |
© Georg Thieme Verlag KG Stuttgart · New York.
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pubmed:issnType |
Electronic
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pubmed:volume |
42
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
28-9
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pubmed:meshHeading |
pubmed-meshheading:21557146-Anticonvulsants,
pubmed-meshheading:21557146-Child, Preschool,
pubmed-meshheading:21557146-Epilepsies, Myoclonic,
pubmed-meshheading:21557146-Humans,
pubmed-meshheading:21557146-Male,
pubmed-meshheading:21557146-Retrospective Studies,
pubmed-meshheading:21557146-Triazoles
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pubmed:year |
2011
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pubmed:articleTitle |
Epilepsy with myoclonic absences - favourable response to add-on rufinamide treatment in 3 cases.
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pubmed:affiliation |
Department of Pediatrics, University Hospital, RWTH Aachen, Aachen, Germany. haeusler@rwth-aachen.de
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pubmed:publicationType |
Journal Article,
Case Reports
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