- ►bmj.com [PDF] N Yamada, TI Chikama, N Morishige, R Yanai, … - British Medical Journal, 2005 - bjo.bmj.com Subconjunctival corticosteroids for benign lymphoid hyperplasia Appropriate
treatment of subconjunctival benign lymphoid hyperplasia (BLH) has been unclear.
Most have noted poor response to oral or topical corticosteroids. Many ... Cited by 3 - Related articles - All 7 versions
E Nakagawa, T Sakimoto, N Inada, J Shoji, … - Nippon Ganka Gakkai Zasshi, 2004 - ncbi.nlm.nih.gov PURPOSE: A histopathological study of lattice corneal dystrophy with L 527 R
mutation of exon 12 on transforming growth factor-beta induced gene(TGFBI).
PATIENT AND METHODS: The patient was a 66-year-old woman with lattice ... Cited by 3 - Related articles - BL Direct - All 2 versions
[CITATION] TGFBI gene mutations in Brazilian patients with corneal dystrophy [published online ahead …
M Kawashima, M Yamada, T Funayama, Y … - Nippon Ganka Gakkai Zasshi, 2005 - ncbi.nlm.nih.gov PURPOSE: To investigate mutations in the transforming growth factor beta induced
(TGFBI) gene and clinical features in 6 Japanese patients who were clinically
diagnosed as having late-onset lattice corneal dystrophy (LCD). METHODS: ... Cited by 5 - Related articles
K Hirano, M Nakamura, N Yamamoto, Y Hotta - JOURNAL-JAPANESE OPHTHALMOLOGICAL …, 2002 - sciencelinks.jp Abstract;Purpose: To investigate the genetics of patients with lattice corneal
dystrophy (LCD) in Aichi Prefecture, the majority of whom originated from the
same area of Hazu-gun. Methods: We studied twenty patients who visited ... Cited by 6 - Related articles - Cached - BL Direct - All 2 versions
K Tsujikawa, M Tsujikawa, S Yamamoto, T … - American journal of medical genetics, 2002 - interscience.wiley.com Lattice corneal dystrophies (LCDs) are caused by mutations of the transforming
growth factor beta-induced gene (TGFBI, formerly ig-h3). LCD type IIIA (LCDIIIA)
has been reported mostly from Japan. In this study, we demonstrate allelic ... Cited by 6 - Related articles - BL Direct - All 3 versions
[CITATION] The clinical utility of genetic analysis in the diagnosis and management of inherited corneal …
AJ Aldave, VS Yellore, CA Self, D Holsclaw, K … - Ophthalmology, 2004 - Elsevier To make ophthalmologists aware of the usefulness of buccal swabs for the
collection of cells from which DNA may be extracted to be used in genetic
screening of patients with known or suspected inherited ocular disorders, ... Cited by 3 - Related articles - All 13 versions
TK Thanh, K Fujiki, A Murakami, A Kanai - Jpn J Ophthalmol, 2003 - nichigan.or.jp Nguyen Thanh Ha*, Le Xuan Cung*,†, Hoang Minh Chau†, Ton Kim Thanh†, Keiko
Fujiki*, Akira Murakami* and Atsushi Kanai* ... *Department of Ophthalmology,
Juntendo University School of Medicine, Tokyo, Japan; †National Institute ... Cited by 7 - Related articles - All 6 versions
T Funayama, Y Mashima, M Kawashima, M … - Japanese journal of ophthalmology, 2006 - Springer Late-onset lattice corneal dystrophy (LCD) is associated with decreasing vision,
minor recurrent epithelial erosions or no erosions at all, and lattice lines
much thicker than those usually observed in LCD types I and II.A patient ... Cited by 7 - Related articles - All 3 versions
