Familial Amyloid Polyneuropathy, Type V

Known as: Finnish Type Familial Amyloid Neuropathy, Type V Familial Amyloid Polyneuropathy, Biber haab dimmer dystrophy 
The presence of fine, branching linear opacities in Bowman's layer in the central area that may spread to the periphery in the clinical course. The… (More)
National Institutes of Health

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Highly Cited
2011
Highly Cited
2011
The UniProt Knowledgebase (UniProtKB) acts as a central hub of protein knowledge by providing a unified view of protein sequence… (More)
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2011
2011
PURPOSE To estimate the prevalence of corneal dystrophies. METHODS Records of almost 8 million enrollees in a national managed… (More)
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2005
2005
PURPOSE To identify mutations in the TGFBI gene in Indian patients with lattice corneal dystrophy (LCD) or granular corneal… (More)
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1999
1999
PURPOSE Two forms of autosomal-dominant lattice corneal dystrophy (LCD), types I and IIIA, have previously been shown to be… (More)
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1998
1998
Reis-Bücklers' corneal dystrophy (RBCD) is a relatively rare autosomal dominant disease originating in the Bowman's membrane… (More)
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1998
1998
PURPOSE To identify the mutation responsible for lattice corneal dystrophy type 1 in an extended Canadian kindred. METHODS A… (More)
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1998
1994
1994
The two most common autosomal dominant dystrophies of the corneal stroma are lattice corneal dystrophy type I and granular… (More)
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1990
1990
Familial amyloidosis, Finnish type (FAF), is an inherited form of systemic amyloidosis clinically characterized by cranial… (More)
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1988
1988
Four patients from families in Pennsylvania, Massachusetts, and Argentina were diagnosed clinically as having granular dystrophy… (More)
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