In Vivo Laser Confocal Microscopy Findings and Mutational Analysis for Schnyder's Crystalline Corneal DystrophyKOBAYASHI, Akira; FUJIKI, Keiko; MURAKAMI, Akira et al.Ophthalmology (Rochester, MN). 2009, Vol 116, Num 6, pp 1029-1037, issn 0161-6420, 9 p.Article

Transferrin-polyethylenimine conjugate, FuGENE6 and TransIT-LT as nonviral vectors for gene transfer to the corneal endotheliumHA NGUYEN THANH; MURAKAMI, Akira; FUJIKI, Keiko et al.Japanese journal of ophthalmology. 2002, Vol 46, Num 2, pp 140-146, issn 0021-5155Article

A novel mutation of M1S1 gene found in a Vietnamese patient with gelatinous droplike corneal dystrophyNGUYEN THANH HA; HOANG MINH CHAU; LE XUAN CUNG et al.American journal of ophthalmology. 2003, Vol 135, Num 3, pp 390-393, issn 0002-9394, 4 p.Article

Multiplex polymerase chain reaction for detection of herpes simplex virus type 1, type 2, cytomegalovirus, and Varicella-Zoster virus in ocular viral infectionsYAN ZHANG; KIMURA, Tairo; FUJIKI, Keiko et al.Japanese journal of ophthalmology. 2003, Vol 47, Num 3, pp 260-264, issn 0021-5155, 5 p.Article

Transthyretin Ser-44 mutation in a case with vitreous amyloidosisMURAKAMI, Akira; FUJIKI, Keiko; HASEGAWA, Sachiko et al.American journal of ophthalmology. 2002, Vol 133, Num 2, pp 272-273, issn 0002-9394Article

OPA1 gene mutations in Japanese patients with bilateral optic atrophy unassociated with mitochondrial DNA mutations at nt 11778, 3460, and 14484YAMADA, Tetsuya; HAYASAKA, Seiji; KANAI, Atsushi et al.Japanese journal of ophthalmology. 2003, Vol 47, Num 4, pp 409-411, issn 0021-5155, 3 p.Article

Q118X mutation of M1S1 gene caused gelatinous drop-like corneal dystrophy : The P501T of BIGH3 gene found in a family with gelatinous drop-like corneal dystrophyNGUYEN THANH HA; FUJIKI, Keiko; HOTTA, Yoshihiro et al.American journal of ophthalmology. 2000, Vol 130, Num 1, pp 119-120, issn 0002-9394Article