Clinical Features of a Newly Recognized Type of Lattice Corneal Dystrophy
- 1 September 1987
- journal article
- research article
- Published by Elsevier in American Journal of Ophthalmology
- Vol. 104 (3) , 241-248
- https://doi.org/10.1016/0002-9394(87)90411-9
Abstract
No abstract availableThis publication has 14 references indexed in Scilit:
- Lattice Dystrophy Type 1: A Report of 8 FamiliesOphthalmologica, 1987
- Familial amyloidosis with cranial neuropathy and corneal lattice dystrophyNeurology, 1986
- Lattice Corneal Dystrophy Associated with Familial Systemic Amyloidosis (Meretoja's Syndrome)Ophthalmology, 1983
- Lattice corneal dystrophy: a source of confusion.British Journal of Ophthalmology, 1983
- Diagnosis of Early Lattice Corneal DystrophyArchives of Ophthalmology (1950), 1982
- The origin of amyloid in gelatinous drop-like corneal dystrophyCurrent Eye Research, 1982
- Familial amyloidosis with cranial neuropathy and corneal lattice dystrophy.Journal of Neurology, Neurosurgery & Psychiatry, 1979
- Primary Familial Amyloidosis of the CorneaAmerican Journal of Ophthalmology, 1976
- Comparative Histopathological and Clinical Findings in Eyes with Lattice Corneal Dystrophy of two Different TypesOphthalmologica, 1972
- LATTICE TYPE OF HEREDITARY CORNEAL DEGENERATIONArchives of Ophthalmology (1950), 1948