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Lafora bodies

An intraneuronal inclusion body composed of acid mucopolysaccharides. [HPO:sdoelken]
National Institutes of Health

Papers overview

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2019
2019
Lafora disease (LD) is a fatal childhood epilepsy caused by recessive mutations in either the EPM2A or EPM2B gene. A hallmark of… Expand
2018
2018
Lafora disease (LD) is a fatal form of progressive myoclonus epilepsy characterized by the accumulation of insoluble poorly… Expand
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Highly Cited
2012
Highly Cited
2012
Lafora disease (LD), a fatal neurodegenerative disorder characterized by the presence of intracellular inclusions called Lafora… Expand
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2012
2012
Lafora disease (LD) is an autosomal recessive, always fatal progressive myoclonus epilepsy with rapid cognitive and neurologic… Expand
Highly Cited
2007
Highly Cited
2007
Lafora disease (LD) is a progressive myoclonic epilepsy resulting in severe neurodegeneration followed by death. A hallmark of LD… Expand
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Highly Cited
2005
Highly Cited
2005
Lafora progressive myoclonus epilepsy, caused by defective laforin or malin, insidiously present in normal teenagers with… Expand
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Highly Cited
2005
Highly Cited
2005
Progressive Myoclonus Epilepsy (PME) of the Lafora type is an autosomal recessive disease, which presents in teenage years with… Expand
Highly Cited
2004
Highly Cited
2004
Lafora disease (LD) is a fatal and the most common form of adolescent-onset progressive epilepsy. Fulminant endoplasmic reticulum… Expand
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1994
1994
Summary: Since age 12 years, a 25‐year‐old woman had a syndrome with myoclonic epilepsy, cerebellar signs, and spontaneous… Expand
Highly Cited
1968
Highly Cited
1968
THE LAFORA body form of myoclonus epilepsy is a genetically-determined (recessive) disease. It usually begins clinically in the… Expand