Temporal macular thinning associated with X-linked Alport syndrome. - Wikidata - wikimedia - TriplyDB

Temporal macular thinning associated with X-linked Alport syndrome.

Temporal macular thinning associated with X-linked Alport syndrome.

http://www.wikidata.org/entity/Q37101426

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Ocular features in Alport syndrome: pathogenesis and clinical significance Retinal Findings on OCT in Systemic Conditions.Alport Syndrome in Women and Girls.Temporal retinal thinning and the diagnosis of Alport syndrome and Thin basement membrane nephropathy.

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Temporal macular thinning associated with X-linked Alport syndrome.

http://www.wikidata.org/entity/Q37101426

description

article científic

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article scientifique

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articolo scientifico

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artigo científico

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bilimsel makale

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scientific article published on June 2013

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vedecký článok

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vetenskaplig artikel

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videnskabelig artikel

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vědecký článek

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name

Temporal macular thinning associated with X-linked Alport syndrome.

@en

Temporal macular thinning associated with X-linked Alport syndrome.

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type

label

Temporal macular thinning associated with X-linked Alport syndrome.

@en

Temporal macular thinning associated with X-linked Alport syndrome.

@nl

prefLabel

Temporal macular thinning associated with X-linked Alport syndrome.

@en

Temporal macular thinning associated with X-linked Alport syndrome.

@nl

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JAMAOPHTHALMOL.2013.1452

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JAMA Ophthalmology

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Temporal macular thinning associated with X-linked Alport syndrome

@en

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Denise J Jones

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

Gregory S Hageman

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Kandon K Kamae

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Margaret M Deangelis

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Martin C Gregory

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Paul S Bernstein

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P2860

X-linked Alport syndrome: natural history and genotype-phenotype correlations in girls and women belonging to 195 families: a "European Community Alport Syndrome Concerted Action" study

Molecular testing for adult type Alport syndrome

Normative data for macular thickness by high-definition spectral-domain optical coherence tomography (spectralis).

Alport retinopathy results from "severe" COL4A5 mutations and predicts early renal failure.

Alport syndrome. An inherited disorder of renal, ocular, and cochlear basement membranes.

Retinal basement membrane abnormalities and the retinopathy of Alport syndrome

Distribution of type IV collagen in the cochlea in Alport syndrome.

A mutation causing Alport syndrome with tardive hearing loss is common in the western United States.

Mapping structural landmarks, ligand binding sites, and missense mutations to the collagen IV heterotrimers predicts major functional domains, novel interactions, and variation in phenotypes in inherited diseases affecting basement membranes.

The renal lesions of Alport syndrome.

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777-782

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scholarly article

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10.1001/JAMAOPHTHALMOL.2013.1452

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2013-06-01T00:00:00Z

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