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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… Expand
National Institutes of Health

Papers overview

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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… Expand
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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… Expand
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Highly Cited
2003
Highly Cited
2003
This Paper examines the importance of agglomeration economies and institutions vis-a-vis initial conditions and factor endowments… Expand
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Highly Cited
2002
Highly Cited
2002
I present data and assess the first twelve years of the transition from plan to market. Transformations have taken place, but the… Expand
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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… Expand
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Highly Cited
2000
Highly Cited
2000
The adoption of Stated Preference (SP) techniques in freight route/mode choice studies requires the identification of the major… Expand
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Highly Cited
1998
Highly Cited
1998
Loss-of-function mutations in the gene (CSTB) encoding human cystatin B, a widely expressed cysteine protease inhibitor, are… Expand
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Highly Cited
1998
Highly Cited
1998
Autosomal dominant nocturnal frontal-lobe epilepsy (ADNFLE) is a recently identified partial epilepsy in which two different… Expand
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Highly Cited
1997
Highly Cited
1997
Progressive myoclonus epilepsy of the Unverricht–Lundborg type (EPM1; MIM 254800) is an autosomal recessive disorder with onset… Expand
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Highly Cited
1995
Highly Cited
1995
The disorder of autosomal dominant nocturnal frontal lobe epilepsy has recently been identified, and is now delineated in detail… Expand
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