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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… 
National Institutes of Health

Papers overview

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2011
2011
Purpose: An atypical case of late-onset lattice corneal dystrophy is described in a 61-year-old man without a family history of… 
2006
2006
OBJECTIVE To describe the clinical data and the results of molecular analyses of the TGFBI gene in a patient with classic… 
2000
2000
Aim—To report a Japanese family diagnosed clinically as having lattice corneal dystrophy type I (LCDI) in which a Leu518Pro… 
1995
1995
Lattice corneal dystrophy type I (LCDI) is a relatively common corneal dystrophy which can cause severe visual impairment. Recent… 
1988
1988
Corneal buttons of two patients with lattice corneal dystrophy were studied by light and electron microscopy. They showed… 
1985
1985
The present study tries to point out new ideas about lattice corneal dystrophy. From our own observations we distinguish five… 
1982
1982
Seven children from two unrelated families had lattice corneal dystrophy. Their ages ranged from 3 to 13 years at initial… 
1978
1978
Most ophthalmologic disorders reported with renal cystic disease have been associated with either medullary cystic disease or… 
Review
1971
Review
1971
Some thoughts on the ultrastructural genesis of the lesions in macular and lattice corneal dystrophy are reviewed. These two… 
1967
1967
Excerpt It is well established that amyloidosis may be a consequence of such disease processes as chronic sepsis, tuberculosis…