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Lafora bodies

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

Related topics

Related topics

1 relation

Broader (1)

Cytoplasmic inclusion (cell structure)

Papers overview

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2013
2013
Exploring the Structural Insights on Human Laforin Mutation K87A in Lafora Disease—A Molecular Dynamics Study
Lafora disease (LD) is an autosomal recessive, progressive form of myoclonus epilepsy which affects worldwide. LD occurs mainly… 
2013
2013
Support Title Homeostatic regulation of emergent neuronal network properties in vivo
The spliceosome is a macromolecular assemblage composed of both proteins and RNA that catalyzes the splicing of transcribed pre… 
2011
2011
Lafora bodies in skeletal muscle are fiber type specific
Glycogen is the largest soluble cytosolic macromolecule, containing up to 55,000 glucoses per molecule. It is formed by glycogen… 
2008
2008
Epilepsia de Lafora
Clinicamente, la enfermedad de Lafora es una forma de epilepsia mioclonica progresiva, autosomica recesiva. Se desarrolla debido… 
2004
2004
Correlation between ultrastructure and histochemistry of lafora bodies
SummaryLafora bodies are composed of fibrillar and granular components in various concentrations. They are located in neuronal… 
2001
2001
Myoclonic epilepsies and Lafora body disease : biopsy diagnosis
Myoclonic epilepsies represent a large group of heterogenous diseases. The most important disorder in this group is Lafora body… 
1994
1994
Arylsulfatase A Pseudodeficiency and Lafora Bodies in a Patient with Progressive Myoclonic Epilepsy
Summary: Since age 12 years, a 25‐year‐old woman had a syndrome with myoclonic epilepsy, cerebellar signs, and spontaneous… 
1991
1991
Early detection of skin and muscular involvement in lafora disease
SummaryTwo siblings with Lafora disease (LD) are described: one with epilepsy, myoclonus, EEG abnormalities, severe dementia and… 
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