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Genus Agrypnia

Known as: Agrypnia 
National Institutes of Health

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
Review
2019
Review
2019
Fatal Familial Insomnia (FFI) is a hereditary prion disease caused by a mutation at codon 178 of the prion-protein gene leading… Expand
2011
2011
Agrypnia excitata (AE) is a syndrome characterized by the inability to sleep associated with a generalized motor and autonomic… Expand
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2011
2011
INTRODUCTION Morvan chorea is an antibody-mediated limbic encephalopathy characterized by severe insomnia, mental confusion… Expand
Review
2011
Review
2011
The concept of Agrypnia excitata (AE) was originally proposed as a concept deriving from the clinical and anatomo-pathological… Expand
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Review
2008
Review
2008
Fatal familial insomnia, a human prion disease, Morvan's chorea, an autoimmune limbic encephalopathy, and delirium tremens, the… Expand
2007
2007
In the serum and cerebrospinal fluid of a patient with recurrent acute episodes of respiratory crises, autonomic symptoms and… Expand
Review
2005
Review
2005
Insomnia is the most common sleep complaint. Insomnia is not a disease itself but mostly a clinical sign of an underlying disease… Expand
Review
2004
Review
2004
This review synthetizes the most important historical contributions in sleep anatomy and the pioneer discoveries in sleep… Expand
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Review
2002
Review
2002
OBJECTIVES To analyse the clinicophysiological features of delirium tremens (DT), Morvan's fibrillary chorea (MC) and fatal… Expand
Highly Cited
2001
Highly Cited
2001
Fatal familial insomnia, Morvan's chorea and delirium tremens share the same clinical features: severe insomnia and mental… Expand