terised by typical choroidal neovascularisation (CNV) that can cause severe vision loss [2]. Polypoidal choroidal vasculopathy (PCV) is an exudative maculopathy marked by branching networks of inner choroidal vessels and a nodular appearance on stereoscopic view with indocyanine green angiography (ICGA) [3]. Emerging evidence has shown that PCV is more common in Asians than in Caucasians [4,5], and it has been recognised as a special ent. Although nAMD and PCV share some common genetic determinants, such as the complement factor H gene (CFH) and the high temperature requirement factor A1 (HTRA1) gene [8,9], they are not the same. For ex-ample, superkiller viralicidic activity 2-like (SKIV2 L), in the entire C2 (complement component 2)-CFB (...
Age related macular degeneration (AMD) in Asians has been suggested to differ from their Western cou...
Copyright © 2014 Raffaella Cascella et al. This is an open access article distributed under the Crea...
<div><p>Purpose</p><p>To investigate whether the polymorphism rs800292 (184G>A, I62V) in the complem...
<b><i>Purpose:</i></b> rs1999930 and rs4711751 have recently been identified as novel variants assoc...
<b><i>Purpose:</i></b> To identify the associations of the two complement factor I (CFI) polymorphis...
Purpose: To identify the associations of the two complement factor I (CFI) polymorphisms rs10033900 ...
PURPOSE: To determine prevalence of probable poly-poidal choroidal vasculopathy (PCV) among White pa...
Purpose: Recently, a complement component 1 inhibitor (SERPING1) gene polymorphism was identified as...
Purpose To investigate the effect of genetic variants in the high-density lipoprotein (HDL) metaboli...
Age-related macular degeneration (AMD) is a complex disorder of the eye and the third leading cause ...
<p>Purpose: To investigate the association of genetic and environmental factors, and their interacti...
Full list of author information is available at the end of the articlemated that the prevalence of A...
Purpose To investigate the association of genetic and environmental factors, and their interactions ...
Age-related macular degeneration (AMD) is the leading cause of irreversible blindness in the elderly...
Complement factor H (CFH) is one of the most important soluble complement regulatory proteins and is...
Age related macular degeneration (AMD) in Asians has been suggested to differ from their Western cou...
Copyright © 2014 Raffaella Cascella et al. This is an open access article distributed under the Crea...
<div><p>Purpose</p><p>To investigate whether the polymorphism rs800292 (184G>A, I62V) in the complem...
<b><i>Purpose:</i></b> rs1999930 and rs4711751 have recently been identified as novel variants assoc...
<b><i>Purpose:</i></b> To identify the associations of the two complement factor I (CFI) polymorphis...
Purpose: To identify the associations of the two complement factor I (CFI) polymorphisms rs10033900 ...
PURPOSE: To determine prevalence of probable poly-poidal choroidal vasculopathy (PCV) among White pa...
Purpose: Recently, a complement component 1 inhibitor (SERPING1) gene polymorphism was identified as...
Purpose To investigate the effect of genetic variants in the high-density lipoprotein (HDL) metaboli...
Age-related macular degeneration (AMD) is a complex disorder of the eye and the third leading cause ...
<p>Purpose: To investigate the association of genetic and environmental factors, and their interacti...
Full list of author information is available at the end of the articlemated that the prevalence of A...
Purpose To investigate the association of genetic and environmental factors, and their interactions ...
Age-related macular degeneration (AMD) is the leading cause of irreversible blindness in the elderly...
Complement factor H (CFH) is one of the most important soluble complement regulatory proteins and is...
Age related macular degeneration (AMD) in Asians has been suggested to differ from their Western cou...
Copyright © 2014 Raffaella Cascella et al. This is an open access article distributed under the Crea...
<div><p>Purpose</p><p>To investigate whether the polymorphism rs800292 (184G>A, I62V) in the complem...