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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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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
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2011
2011
Glycogen is the largest soluble cytosolic macromolecule, containing up to 55,000 glucoses per molecule. It is formed by glycogen… Expand
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2009
2009
BackgroundLafora disease (LD) is a fatal autosomal recessive neurodegenerative disease. A hallmark of LD is cytoplasmic… Expand
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2007
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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2005
2005
Progressive Myoclonus Epilepsy (PME) of the Lafora type is an autosomal recessive disease, which presents in teenage years with… Expand
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1994
1994
Since age 12 years, a 25-year-old woman had a syndrome with myoclonic epilepsy, cerebellar signs, and spontaneous myoclonus. Skin… Expand
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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
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