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Cited by 753

The DOI matches its Crossref record; 1 of the 1 references it cites were found in a registry or an index.

IDIOPATHIC POLYPOIDAL CHOROIDAL VASCULOPATHY (IPCV)

Yannuzzi, Lawrence A., Sorenson, John, Spaide, Richard F., Lipson, Barry·2012·Retina

Abstract

Eleven patients, 40 to 71 years old, had a choroidal vasculopathy that led to hemorrhagic and exudative macular degeneration. The patients had peculiar polypoidal, subretinal, vascular lesions associated with serous and hemorrhagic detachments of the retinal pigment epithelium. This macular disorder, which we have named idiopathic polypoidal choroidal vasculopathy (IPCV), appears to represent a distinct entity that differs clinically and demograph-ically from age-related macular degeneration (AMD) and other macular diseases associated with subretinal neovascularization. Recognition of this condition is important because it may have specific risk factors, natural course, and management considerations that differ from those of age-related macular degeneration

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Crossref · 10.1097/iae.0b013e31823f992a

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Metadata

Authors
Yannuzzi, L. A., Sorenson, J., Spaide, R. F., & Lipson, B.
Venue
Retina
Published
2012-02
Volume
32
Issue
Supplement 1
Pages
1-8
ISSN
0275-004X (ISSN-L)
OpenAlex
W1978913875
Cited by
753
References
1
FWCI
43.76
Type
journal article
Language
en
Open access
closed

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CoChat. (2026). Citation check: IDIOPATHIC POLYPOIDAL CHOROIDAL VASCULOPATHY (IPCV). https://app.cochat.ai/papers/10.1097/iae.0b013e31823f992a
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Yannuzzi, L. A., Sorenson, J., Spaide, R. F., & Lipson, B. (2012). IDIOPATHIC POLYPOIDAL CHOROIDAL VASCULOPATHY (IPCV). Retina. https://doi.org/10.1097/iae.0b013e31823f992a

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