Protein Aa and Lattice Corneal Dystrophy

Author:

Mondino Bartly J.,Raj Cholappadi V. Sundar,Skinner Martha,Cohen Alan S.,Brown Stuart I.

Publisher

Elsevier BV

Subject

Ophthalmology

Reference8 articles.

1. The complexity of amyloid;Franklin;New Engl. J. Med.,1974

2. Amyloidosis. Current trends in its investigation;Cohen;Arthritis Rheum.,1978

3. Amyloid fibril protein related to prealbumin in familial amyloidotic polyneuropathy;Costa;Proc. Natl. Acad. Sci. U.S.A.,1978

4. The identification of amyloid P-component (protein AP) in normal cultured human fibroblasts;Spark;Lab. Invest.,1978

5. Lattice corneal dystrophy. An inherited variety of amyloidosis restricted to the cornea;Klintworth;Am. J. Pathol.,1967

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1. Corneal Dysgeneses, Dystrophies, and Degenerations;Albert and Jakobiec's Principles and Practice of Ophthalmology;2022

2. Corneal Dysgeneses, Dystrophies, and Degenerations;Albert and Jakobiec's Principles and Practice of Ophthalmology;2021

3. Corneal Dysgeneses, Dystrophies, and Degenerations;Albert &amp Jakobiec's Principles &amp Practice of Ophthalmology;2008

4. Confocal microscopy in lattice corneal dystrophy;Graefe's Archive for Clinical and Experimental Ophthalmology;1999-07-05

5. Ocular amyloidosis, with special reference to thehereditary forms with vitreous involvement;Survey of Ophthalmology;1995-11

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