Amyloid Neuropathies

Known as: Neuropathies, Amyloid, amyloidosis polyneuropathy, Amyloid Neuropathies [Disease/Finding] 
Disorders of the peripheral nervous system associated with the deposition of AMYLOID in nerve tissue. Familial, primary (nonfamilial), and secondary… (More)
National Institutes of Health

Papers overview

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Highly Cited
2013
Highly Cited
2013
Tafamidis, a transthyretin (TTR) kinetic stabilizer, delayed neuropathic progression in patients with Val30Met TTR familial… (More)
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Highly Cited
2012
Highly Cited
2012
OBJECTIVES To evaluate the efficacy and safety of 18 months of tafamidis treatment in patients with early-stage V30M… (More)
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Highly Cited
2012
Highly Cited
2012
The transthyretin amyloidoses (ATTR) are invariably fatal diseases characterized by progressive neuropathy and/or cardiomyopathy… (More)
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Review
2011
Review
2011
Familial amyloid polyneuropathies (FAPs) are a group of life-threatening multisystem disorders transmitted as an autosomal… (More)
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Highly Cited
2010
Highly Cited
2010
The Nomenclature Committee of the International Society of Amyloidosis (ISA) met during the XIIIth International Symposium, May 6… (More)
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Review
2007
Review
2007
Neuropathy is often a major manifestation of systemic amyloidosis. It is most frequently seen in patients with hereditary… (More)
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Review
2002
Review
2002
Alzheimer's disease (AD) is a progressive, neurodegenerative disorder characterized by amyloid deposition in the cerebral… (More)
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Review
2001
Review
2001
Amyloid neuropathies occur in a context of hereditary (FAP) or acquired amyloidosis. They present usually as severe and… (More)
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Highly Cited
2000
Highly Cited
2000
Familial amyloid polyneuropathy (FAP) associated with mutations of the transthyretin (TTR) gene is the most common type of FAP, a… (More)
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Highly Cited
1993
Highly Cited
1993
Familial amyloid polyneuropathy (FAP) is a fatal autosomal dominant disorder. Progressive peripheral and autonomic neuropathy are… (More)
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