Amyloidosis, Familial

Known as: amyloidosis familial, Familial Amyloidoses, Familial Amyloidosis 
Diseases in which there is a familial pattern of AMYLOIDOSIS.
National Institutes of Health

Papers overview

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Highly Cited
2004
Highly Cited
2004
Transthyretin (TTR) tetramer dissociation and misfolding affords a monomeric amyloidogenic intermediate that misassembles into… (More)
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Review
1998
Review
1998
  • Sari Kiuru
  • Amyloid : the international journal of…
  • 1998
Gelsolin-related familial amyloidosis, Finnish type, occurs worldwide, most likely as a result of sporadic low-frequency… (More)
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Highly Cited
1997
Highly Cited
1997
OBJECTIVE To determine whether patients with myocardial amyloidosis due either to AL (primary) amyloid or familial amyloid have… (More)
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1997
1997
BACKGROUND Familial amyloidosis (FAP) is characterized by the progression of neurologic and cardiac impairment ultimately leading… (More)
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1996
1996
Amyloid deposits in leptomeningeal vessels, subarachnoid, subpial, and subependymal cerebrospinal regions, spinal ganglia… (More)
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Highly Cited
1992
Highly Cited
1992
Dominantly inherited familial amyloidosis, Finnish type (FAF) is caused by the accumulation of a 71–amino acid amyloidogenic… (More)
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1992
1992
Between 1961 and 1990, 52 patients with biopsy-proven familial amyloidosis born in North America were examined at the Mayo Clinic… (More)
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Highly Cited
1984
Highly Cited
1984
Amyloid fibril protein in patients with familial amyloidotic polyneuropathy is known to be chemically related to transthyretin… (More)
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1976
1976
A case of primary familial amyloidosis of the cornea in a 13-year-old boy was confirmed by histopathologic examination of… (More)
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1975
1975
The pathology of primary familia amyloidosis with polyneuropathy is described on the basis of post-mortem examination of six… (More)
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