Unverricht-Lundborg Syndrome

Known as: EPILEPSY, PROGRESSIVE MYOCLONIC, 1, EPILEPSY, PROGRESSIVE MYOCLONIC, 1A, Mediterranean Myoclonic Epilepsy 
An autosomal recessive condition characterized by recurrent myoclonic and generalized seizures, ATAXIA, slowly progressive intellectual deterioration… (More)
National Institutes of Health

Papers overview

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Highly Cited
2012
Highly Cited
2012
The purpose of this study was to assess the diagnostic image quality of ultra-low-dose chest computed tomography (ULD-CT… (More)
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Highly Cited
2010
Highly Cited
2010
N-methyl-D-aspartate (NMDA) receptors mediate excitatory neurotransmission in the mammalian brain. Two glycine-binding NR1… (More)
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Highly Cited
2010
Highly Cited
2010
This paper presents estimations of the shadow economies for 162 countries, including developing, Eastern European, Central Asian… (More)
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Review
2008
Review
2008
Unverricht-Lundborg disease (ULD), progressive myoclonic epilepsy type 1 (EPM1, OMIM254800), is an autosomal recessively… (More)
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2007
2007
PURPOSE Unverricht-Lundborg disease (ULD) is currently classified as progressive myoclonus epilepsy. Myoclonus, the… (More)
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2006
2006
PURPOSE To assess the long-term evolution of Unverricht-Lundborg disease (ULD), especially concerning myoclonus, seizures, and… (More)
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Highly Cited
2003
Highly Cited
2003
The views expressed in this Working Paper are those of the author(s) and do not necessarily represent those of the IMF or IMF… (More)
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Highly Cited
2001
Highly Cited
2001
BACKGROUND The genetic basis of most common forms of human paroxysmal disorders of the central nervous system, such as epilepsy… (More)
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Highly Cited
2001
Highly Cited
2001
T he collapse of the Soviet political and economic system in the late 1980s, epitomized by the fall of the Berlin Wall in… (More)
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Highly Cited
1992
Highly Cited
1992
Pectin methylesterase (PME, EC 3.1.11) demethoxylates pectins and is believed to be involved in degradation of pectic cell wall… (More)
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