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- Journal Article
- A2
- open access
Complicated spastic paraplegia in patients with AP5Z1 mutations (SPG48)
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- Journal Article
- A1
- open access
Rare mutations in SQSTM1 modify susceptibility to frontotemporal lobar degeneration
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- Journal Article
- A1
- open access
First line management of prolonged convulsive seizures in children and adults : good practice points
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- Journal Article
- A1
- open access
Recommendations for the treatment of epilepsy in adult patients in general practice in Belgium : an update
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KCNQ2 encephalopathy: emerging phenotype of a neonatal epileptic encephalopathy
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Progressive myoclonic epilepsy as an adult-onset manifestation of Leigh syndrome due to the m.14487T>C mutation in ND6