Amyloidosis, Hereditary

Known as: Amyloidoses, Hereditary, Amyloidosis - hereditaries, Amyloidosis - hereditary 
Diseases in which there is an inherited mutation leading to AMYLOIDOSIS.
National Institutes of Health

Papers overview

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2014
2014
Hereditary systemic amyloidosis comprises a group of rare monogenic diseases inherited in an autosomal dominant fashion. It is… (More)
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Review
2013
Review
2013
Transthyretin amyloidosis is a progressive and eventually fatal disease primarily characterized by sensory, motor, and autonomic… (More)
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Highly Cited
2006
Highly Cited
2006
Investigators in the United Kingdom have shown that hereditary amyloidosis can be misdiagnosed as Ig light-chain (AL) amyloidosis… (More)
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Highly Cited
2002
Highly Cited
2002
BACKGROUND Hereditary, autosomal dominant amyloidosis, caused by mutations in the genes encoding transthyretin, fibrinogen A… (More)
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2002
2002
BACKGROUND The number of proteins with mutations resulting in amyloidosis has continued to increase. Five proteins--transthyretin… (More)
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2001
2001
Hereditary systemic amyloidosis may be caused by mutations in a number of plasma proteins including transthyretin, apolipoprotein… (More)
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Review
1999
Review
1999
Amyloidosis is a generic term for a heterogeneous group of disorders associated with deposition of protein in an abnormal… (More)
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1993
1993
Three members of a family who died with renal amyloidosis were found to share a single nucleotide substitution in the fibrinogen… (More)
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1990
1990
The amyloid protein in Finnish hereditary amyloidosis is a fragment of the actin-filament binding region of a variant gelsolin… (More)
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1990
1990
Familial amyloidosis, Finnish type (FAF), is an autosomal dominant form of familial amyloid polyneuropathy. The novel amyloid… (More)
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