- ►nih.gov - Free from Publisher H Esfandiary, U Chakravarthy, C Patterson, … - British Journal of Ophthalmology, 2005 - bjo.bmj.com Background/aims: Age related macular degeneration (AMD) is a complex disorder
leading to loss of central vision, and identification of risk factors associated
with susceptibility to AMD has been a key objective for ophthalmic genetics ... Cited by 11 - Related articles - All 9 versions
PN Baird, D Chu, E Guida, HTV Vu, R Guymer - American journal of ophthalmology, 2004 - Elsevier To investigate the reported association of the two single-nucleotide
polymorphisms (SNPs) of the paraoxonase gene (PON1), Met-Leu 55 (M55L) and
Gln-Arg 192 (Q192R), in individuals of Anglo-Celtic descent who have ... Cited by 12 - Related articles - All 13 versions
N Fiotti, M Pedio, MB Parodi, N Altamura, L … - Genetics in Medicine, 2005 - journals.lww.com From the Departments of 1 Clinical, Morphological and Technological Sciences,
and 2 Surgical Specialties Sciences of the University of Trieste, Trieste,
Italy; and 3 Blood Transfusion Center, ASS 1 triestina, Trieste, Italy. Cited by 18 - Related articles - All 3 versions
N Gotoh, R Yamada, F Matsuda, N Yoshimura, … - American Journal of Ophthalmology, 2008 - ajo.com Register or Login: Password: Auto-Login [Reminder]. Search This Periodical for. ... Cited by 2 - Related articles - Cached - All 12 versions
N Gotoh, S Kuroiwa, T Kikuchi, J Arai, S Arai … - American journal of ophthalmology, 2004 - Elsevier Apo E ε3/ε3 was the most frequent genotype with a prevalence of 79.3% in PCV
patients, 76.5% in AMD patients, and 67.1% in the control subjects. However, the
differences in the percentages were not statistically significant among the ... Cited by 18 - Related articles - All 14 versions
- ►iovs.org S Schmidt, EA Postel, A Agarwal, IC Allen Jr, … - Investigative ophthalmology & visual science, 2003 - ARVO PURPOSE. Age-related maculopathy (ARM) is one of the most common causes of
blindness in older adults worldwide. Sequence variants in a gene coding for a
retina-specific ATP-binding cassette (ABCA4) transporter protein, which is ... Cited by 19 - Related articles - BL Direct - All 4 versions
A Akimoto, M Akimoto, S Kuroiwa, T Kikuchi, … - Graefe's Archive for Clinical and Experimental …, 2001 - Springer Abstract Background: Heterozy- gous mutations of the bestrophin gene are
associated with Best macu- lar dystrophy (BMD). The bestro- phin gene is
specifically expressed in the retinal pigment epithelium. BMD is a ... Cited by 11 - Related articles - BL Direct - All 3 versions
BS Shastry, MT Trese - Ophthalmologica, 2000 - content.karger.com Age-related macular degeneration (AMD) is a heterogeneous group of disorders and
is the leading cause of blindness in the elderly. While degeneration changes in
the macula can occur at any time in life, it is the most common cause of ... Cited by 20 - Related articles - BL Direct - All 5 versions
