| pubmed-article:21393095 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:21393095 | lifeskim:mentions | umls-concept:C0036572 | lld:lifeskim |
| pubmed-article:21393095 | lifeskim:mentions | umls-concept:C0543467 | lld:lifeskim |
| pubmed-article:21393095 | lifeskim:mentions | umls-concept:C0038505 | lld:lifeskim |
| pubmed-article:21393095 | lifeskim:mentions | umls-concept:C1274040 | lld:lifeskim |
| pubmed-article:21393095 | lifeskim:mentions | umls-concept:C1533148 | lld:lifeskim |
| pubmed-article:21393095 | lifeskim:mentions | umls-concept:C0332162 | lld:lifeskim |
| pubmed-article:21393095 | lifeskim:mentions | umls-concept:C0441988 | lld:lifeskim |
| pubmed-article:21393095 | pubmed:issue | 1 | lld:pubmed |
| pubmed-article:21393095 | pubmed:dateCreated | 2011-4-4 | lld:pubmed |
| pubmed-article:21393095 | pubmed:abstractText | Sturge-Weber syndrome is a neurocutaneous disorder classically characterized by the presence of facial port-wine stain and ipsilateral leptomeningeal angiomatosis. It is often associated with refractory epilepsy which requires surgical treatment. We present a case of a patient who initially presented with partial seizures of temporo-occipital origin, ipsilateral to the pial angiomatosis. During the course of the disease, the patient developed medically refractory epilepsy with partial seizures originating predominantly from the contralateral temporo-occipital area as well as myoclonic and myoclonic-astatic seizures. Resection of the occipital and temporal lobe affected by the pial angioma resulted in favourable outcome. Bilateral dysfunction observed in Sturge-Weber syndrome may result in an increased capability of focal discharges to generate synchronous epileptiform activity leading to an increased incidence of generalised seizures, most probably via a mechanism of secondary bilateral synchrony. [Published with video sequences]. | lld:pubmed |
| pubmed-article:21393095 | pubmed:language | eng | lld:pubmed |
| pubmed-article:21393095 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:21393095 | pubmed:citationSubset | IM | lld:pubmed |
| pubmed-article:21393095 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:21393095 | pubmed:month | Mar | lld:pubmed |
| pubmed-article:21393095 | pubmed:issn | 1294-9361 | lld:pubmed |
| pubmed-article:21393095 | pubmed:author | pubmed-author:MarusicPetrP | lld:pubmed |
| pubmed-article:21393095 | pubmed:author | pubmed-author:JefferysJohn... | lld:pubmed |
| pubmed-article:21393095 | pubmed:author | pubmed-author:KrsekPavelP | lld:pubmed |
| pubmed-article:21393095 | pubmed:author | pubmed-author:JiruskaPremys... | lld:pubmed |
| pubmed-article:21393095 | pubmed:author | pubmed-author:KomarekVladim... | lld:pubmed |
| pubmed-article:21393095 | pubmed:author | pubmed-author:CmejlaRomanR | lld:pubmed |
| pubmed-article:21393095 | pubmed:author | pubmed-author:SebronovaVera... | lld:pubmed |
| pubmed-article:21393095 | pubmed:issnType | Print | lld:pubmed |
| pubmed-article:21393095 | pubmed:volume | 13 | lld:pubmed |
| pubmed-article:21393095 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:21393095 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:21393095 | pubmed:pagination | 76-81 | lld:pubmed |
| pubmed-article:21393095 | pubmed:meshHeading | pubmed-meshheading:21393095... | lld:pubmed |
| pubmed-article:21393095 | pubmed:meshHeading | pubmed-meshheading:21393095... | lld:pubmed |
| pubmed-article:21393095 | pubmed:meshHeading | pubmed-meshheading:21393095... | lld:pubmed |
| pubmed-article:21393095 | pubmed:meshHeading | pubmed-meshheading:21393095... | lld:pubmed |
| pubmed-article:21393095 | pubmed:meshHeading | pubmed-meshheading:21393095... | lld:pubmed |
| pubmed-article:21393095 | pubmed:meshHeading | pubmed-meshheading:21393095... | lld:pubmed |
| pubmed-article:21393095 | pubmed:meshHeading | pubmed-meshheading:21393095... | lld:pubmed |
| pubmed-article:21393095 | pubmed:meshHeading | pubmed-meshheading:21393095... | lld:pubmed |
| pubmed-article:21393095 | pubmed:year | 2011 | lld:pubmed |
| pubmed-article:21393095 | pubmed:articleTitle | Sturge-Weber syndrome: a favourable surgical outcome in a case with contralateral seizure onset and myoclonic-astatic seizures. | lld:pubmed |
| pubmed-article:21393095 | pubmed:affiliation | Neuronal Networks Group, Neuropharmacology and Neurobiology, School of Clinical and Experimental Medicine, University of Birmingham, Birmingham, United Kingdom. | lld:pubmed |
| pubmed-article:21393095 | pubmed:publicationType | Journal Article | lld:pubmed |
| pubmed-article:21393095 | pubmed:publicationType | Case Reports | lld:pubmed |
| pubmed-article:21393095 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
