Recent Publications on Unverricht-Lundborg Syndrome: |  |
Unverricht-Lundborg progressive myoclonus epilepsy in Oman.
We analyzed the clinical, electrophysiologic, and genetic features of...
Direct Link | 11th July, 2008
| Department of Neurology, Royal Hospital, Muscat, Oman.
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Clinical picture of EPM1-Unverricht-Lundborg disease.
Unverricht-Lundborg disease (ULD), progressive myoclonic epilepsy type 1...
Direct Link | 23rd May, 2008
| Kuopio Epilepsy Center, Department of Neurology, Kuopio University
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Molecular background of EPM1-Unverricht-Lundborg disease.
Unverricht-Lundborg disease (EPM1) is an autosomal recessively inherited...
Direct Link | 23rd May, 2008
| Folkhalsan Institute of Genetics and Neuroscience Center, Biomedicum
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The natural history of Unverricht-Lundborg disease: a report of eight genetically proven cases.
We report eight cases of genetically proven ULD, with the aim of...
Direct Link | 15th April, 2008
| Sobell Department of Motor Neuroscience and Movement Disorders, Institute
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Substantial thalamostriatal dopaminergic defect in Unverricht-Lundborg disease.
PURPOSE: Unverricht-Lundborg disease (ULD) is currently classified as...
Direct Link | 11th October, 2007
| Department of Neurology, Turku University Hospital, Turku, Finland.
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Levetiracetam in three cases of progressive myoclonus epilepsy.
We present three unrelated cases of genetically confirmed progressive...
Direct Link | 19th August, 2007
| The Cyprus Institute of Neurology & Genetics, Nicosia, Cyprus.
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Seizures, ataxia, and neuronal loss in cystatin B heterozygous mice.
Unverricht-Lundborg disease (EPM1) has been considered to be an...
Direct Link | 7th July, 2007
| Department of Pharmacology, Centre of Excellence of Molecular and Clinical
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A pathogenetic hypothesis of Unverricht-Lundborg disease onset and progression.
Unverricht-Lundborg disease (EPM1), the most common progressive myoclonic...
Direct Link | 18th May, 2007
| Division of Neurophysiology and Epileptology, Neurological Institute C.
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Long-term evolution of EEG in Unverricht-Lundborg disease.
PURPOSE: Unverricht-Lundborg disease (ULD) is a progressive myoclonus...
Direct Link | 16th May, 2007
| Centre for the Diagnosis and Care of Epilepsy, Department of
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Hyperostosis frontalis interna as a novel finding in Unverricht-Lundborg disease.
PURPOSE: Unverricht-Lundborg disease (ULD) is currently classified as...
Direct Link | 26th April, 2007
| Department of Neurology, Turku University Hospital, Kiinamyllynkatu 4-8,
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Cystatin B: mutation detection, alternative splicing and expression in progressive myclonus epilepsy of Unverricht-Lundborg type (EPM1) patients.
Progressive myoclonus epilepsy of Unverricht-Lundborg type (EPM1) is an...
Direct Link | 17th March, 2007
| Department of Medical Genetics and Neuroscience Center, Folkhalsan
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Lack of efficacy and potential aggravation of myoclonus with lamotrigine in Unverricht-Lundborg disease.
PURPOSE: Unverricht-Lundborg disease (ULD) is a progressive myoclonus...
Direct Link | 25th January, 2007
| Centre Saint Paul-H. Gastaut, Marseille, France.
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Protein therapy for Unverricht-Lundborg disease using cystatin B transduction by TAT-PTD. Is it that simple?
In this work we analysed the characteristics of the cell-permeable peptide...
Direct Link | 19th January, 2007
| Department of Molecular and Medical Genetics, University of Toronto,
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Altered tryptophan metabolism in the brain of cystatin B-deficient mice: a model system for progressive myoclonus epilepsy.
PURPOSE: Progressive myoclonus epilepsy of the Unverricht-Lundborg type...
Direct Link | 13th December, 2006
| Department of Pharmacology, University of Tartu, Tartu, Estonia.
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[Unverricht-Lundborg disease (PME1)]
Unverricht-Lundborg disease (ULD) is the purest and least severe type of...
Direct Link | 15th November, 2006
| Centre Saint-Paul--H.
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