Fundus autofluorescence, optical coherence tomography, and electroretinogram findings in choroidal sclerosis - Wikidata - wikimedia - TriplyDB

Fundus autofluorescence, optical coherence tomography, and electroretinogram findings in choroidal sclerosis

Fundus autofluorescence, optical coherence tomography, and electroretinogram findings in choroidal sclerosis

http://www.wikidata.org/entity/Q33937657

about

Two-photon excited autofluorescence imaging of freshly isolated frog retinas.Clinical characteristics of a large choroideremia pedigree carrying a novel CHM mutation.

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P2860

Fundus autofluorescence, optical coherence tomography, and electroretinogram findings in choroidal sclerosis

http://www.wikidata.org/entity/Q33937657

description

2010 nî lūn-bûn

@nan

2010 թուականի Յուլիսին հրատարակուած գիտական յօդուած

@hyw

2010 թվականի հուլիսին հրատարակված գիտական հոդված

@hy

2010年の論文

@ja

2010年論文

@yue

2010年論文

@zh-hant

2010年論文

@zh-hk

2010年論文

@zh-mo

2010年論文

@zh-tw

2010年论文

@wuu

name

Fundus autofluorescence, optic ...... indings in choroidal sclerosis

@ast

Fundus autofluorescence, optic ...... indings in choroidal sclerosis

@en

type

label

Fundus autofluorescence, optic ...... indings in choroidal sclerosis

@ast

Fundus autofluorescence, optic ...... indings in choroidal sclerosis

@en

prefLabel

Fundus autofluorescence, optic ...... indings in choroidal sclerosis

@ast

Fundus autofluorescence, optic ...... indings in choroidal sclerosis

@en

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Fundus autofluorescence, optic ...... indings in choroidal sclerosis

@en

P2093

Chai Lin Chou

http://www.w3.org/2001/XMLSchema#string

David Y Kim

http://www.w3.org/2001/XMLSchema#string

Stephen H Tsang

http://www.w3.org/2001/XMLSchema#string

P2860

Newfoundland rod-cone dystrophy, an early-onset retinal dystrophy, is caused by splice-junction mutations in RLBP1

Ocular phenotype of bothnia dystrophy, an autosomal recessive retinitis pigmentosa associated with an R234W mutation in the RLBP1 gene

Fundus autofluorescence and development of geographic atrophy in age-related macular degeneration.

Annular choroidal sclerosis.

Fluorescein angiography of the hereditary choroidal dystrophies.

Mutation in a short-chain collagen gene, CTRP5, results in extracellular deposit formation in late-onset retinal degeneration: a genetic model for age-related macular degeneration.

Central areolar choroidal sclerosis.

Generalized choroidal sclerosis; course and mode of inheritance.

Choroidal atrophy. Clinical and genetic types.

Functional characteristics of patients with retinal dystrophy that manifest abnormal parafoveal annuli of high density fundus autofluorescence; a review and update

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1095-1103

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scholarly article

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10.1097/IAE.0B013E3181CD48F9

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7

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30

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2010-07-01T00:00:00Z

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41910731

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20224472

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2891359

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