| pubmed-article:15129840 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:15129840 | lifeskim:mentions | umls-concept:C0008059 | lld:lifeskim |
| pubmed-article:15129840 | lifeskim:mentions | umls-concept:C1457887 | lld:lifeskim |
| pubmed-article:15129840 | lifeskim:mentions | umls-concept:C0036572 | lld:lifeskim |
| pubmed-article:15129840 | lifeskim:mentions | umls-concept:C0006118 | lld:lifeskim |
| pubmed-article:15129840 | lifeskim:mentions | umls-concept:C0449450 | lld:lifeskim |
| pubmed-article:15129840 | pubmed:issue | 2 | lld:pubmed |
| pubmed-article:15129840 | pubmed:dateCreated | 2004-5-7 | lld:pubmed |
| pubmed-article:15129840 | pubmed:abstractText | Seizures were the presenting clinical symptom in 10 (12%) of 81 consecutive children with a primary brain tumour treated in a tertiary paediatric oncology unit over 5 years. Nine patients experienced partial seizures, and in seven a waking electroencephalogram showed focal or lateralising abnormalities. Astrocytoma was the most common tumour histology. The delay in tumour diagnosis from the onset of seizures ranged from 2 weeks to 2 years with a mean of 6 months. Complete resection of the tumour was the only treatment in three patients and four underwent resection followed by radiotherapy and/or chemotherapy. Two patients died. Three patients became seizure free receiving no antiepileptic medication and the remaining five showed a 50-80% reduction in seizures between 2 and almost 5 years following treatment. | lld:pubmed |
| pubmed-article:15129840 | pubmed:language | eng | lld:pubmed |
| pubmed-article:15129840 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:15129840 | pubmed:citationSubset | IM | lld:pubmed |
| pubmed-article:15129840 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:15129840 | pubmed:month | Mar | lld:pubmed |
| pubmed-article:15129840 | pubmed:issn | 1059-1311 | lld:pubmed |
| pubmed-article:15129840 | pubmed:author | pubmed-author:AppletonRicha... | lld:pubmed |
| pubmed-article:15129840 | pubmed:author | pubmed-author:IbrahimKhalid... | lld:pubmed |
| pubmed-article:15129840 | pubmed:issnType | Print | lld:pubmed |
| pubmed-article:15129840 | pubmed:volume | 13 | lld:pubmed |
| pubmed-article:15129840 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:15129840 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:15129840 | pubmed:pagination | 108-12 | lld:pubmed |
| pubmed-article:15129840 | pubmed:dateRevised | 2004-11-17 | lld:pubmed |
| pubmed-article:15129840 | pubmed:meshHeading | pubmed-meshheading:15129840... | lld:pubmed |
| pubmed-article:15129840 | pubmed:meshHeading | pubmed-meshheading:15129840... | lld:pubmed |
| pubmed-article:15129840 | pubmed:meshHeading | pubmed-meshheading:15129840... | lld:pubmed |
| pubmed-article:15129840 | pubmed:meshHeading | pubmed-meshheading:15129840... | lld:pubmed |
| pubmed-article:15129840 | pubmed:meshHeading | pubmed-meshheading:15129840... | lld:pubmed |
| pubmed-article:15129840 | pubmed:meshHeading | pubmed-meshheading:15129840... | lld:pubmed |
| pubmed-article:15129840 | pubmed:meshHeading | pubmed-meshheading:15129840... | lld:pubmed |
| pubmed-article:15129840 | pubmed:meshHeading | pubmed-meshheading:15129840... | lld:pubmed |
| pubmed-article:15129840 | pubmed:meshHeading | pubmed-meshheading:15129840... | lld:pubmed |
| pubmed-article:15129840 | pubmed:meshHeading | pubmed-meshheading:15129840... | lld:pubmed |
| pubmed-article:15129840 | pubmed:year | 2004 | lld:pubmed |
| pubmed-article:15129840 | pubmed:articleTitle | Seizures as the presenting symptom of brain tumours in children. | lld:pubmed |
| pubmed-article:15129840 | pubmed:affiliation | The Roald Dahl EEG Unit, Department of Neurology, Royal Liverpool Children's NHS Trust (Alder Hey), Liverpool, UK. | lld:pubmed |
| pubmed-article:15129840 | pubmed:publicationType | Journal Article | lld:pubmed |
