Unverricht-Lundborg disease, a condition with self-limited progression: long-term follow-up of 20 patients.
about
Profile of brivaracetam and its potential in the treatment of epilepsyClinical picture of EPM1-Unverricht-Lundborg disease3D texture analysis reveals imperceptible MRI textural alterations in the thalamus and putamen in progressive myoclonic epilepsy type 1, EPM1.The network sustaining action myoclonus: a MEG-EMG study in patients with EPM1.Progressive myoclonic epilepsies: definitive and still undetermined causes.Genetics of epilepsy and relevance to current practice.Broad spectrum of hepatocyte inclusions in humans, animals, and experimental models.Transition for patients with epilepsy due to metabolic and mitochondrial disorders.Progressive myoclonic epilepsy type 1: Report of an Emirati family and literature review.Brivaracetam: review of its pharmacology and potential use as adjunctive therapy in patients with partial onset seizures.Update on pharmacological treatment of Progressive Myoclonus Epilepsies.Methodological issues associated with clinical trials in epilepsy.Myoclonus epilepsy and ataxia due to KCNC1 mutation: Analysis of 20 cases and K+ channel properties.Description of a family with a novel progressive myoclonus epilepsy and cognitive impairment.Clinical and neurophysiological features of familial cortical myoclonic tremor with epilepsy.Alterations of motor cortical excitability and anatomy in Unverricht-Lundborg disease.Levetiracetam-responsive myoclonus in spinocerebellar ataxia type 15.Severer phenotype in Unverricht-Lundborg disease (EPM1) patients compound heterozygous for the dodecamer repeat expansion and the c.202C>T mutation in the CSTB gene.The photoparoxysmal response: the probable cause of attacks during video games.'North Sea' progressive myoclonus epilepsy: phenotype of subjects with GOSR2 mutation.Clinical and neurophysiologic features of progressive myoclonus epilepsy without renal failure caused by SCARB2 mutations.Cerebellar Involvement in Patients with Mild to Moderate Myoclonus Due to EPM1: Structural and Functional MRI Findings in Comparison with Healthy Controls and Ataxic Patients.Natural history and long-term evolution in families with autosomal dominant cortical tremor, myoclonus, and epilepsy.Perampanel in 12 patients with Unverricht-Lundborg disease.
P2860
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P2860
Unverricht-Lundborg disease, a condition with self-limited progression: long-term follow-up of 20 patients.
description
2006 nî lūn-bûn
@nan
2006年の論文
@ja
2006年論文
@yue
2006年論文
@zh-hant
2006年論文
@zh-hk
2006年論文
@zh-mo
2006年論文
@zh-tw
2006年论文
@wuu
2006年论文
@zh
2006年论文
@zh-cn
name
Unverricht-Lundborg disease, a ...... term follow-up of 20 patients.
@en
Unverricht-Lundborg disease, a ...... term follow-up of 20 patients.
@nl
type
label
Unverricht-Lundborg disease, a ...... term follow-up of 20 patients.
@en
Unverricht-Lundborg disease, a ...... term follow-up of 20 patients.
@nl
prefLabel
Unverricht-Lundborg disease, a ...... term follow-up of 20 patients.
@en
Unverricht-Lundborg disease, a ...... term follow-up of 20 patients.
@nl
P2093
P2860
P1433
P1476
Unverricht-Lundborg disease, a ...... -term follow-up of 20 patients
@en
P2093
Edoardo Ferlazzo
Pierre Genton
Vi-Hong Nguyen
P2860
P304
P356
10.1111/J.1528-1167.2006.00553.X
P577
2006-05-01T00:00:00Z