Temporal retinal thinning and the diagnosis of Alport syndrome and Thin basement membrane nephropathy-Reference-Cited by-同舟云学术

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Temporal retinal thinning and the diagnosis of Alport syndrome and Thin basement membrane nephropathy

Published:2017-11-27 Issue:2 Volume:39 Page:208-214
ISSN:1381-6810
Container-title:Ophthalmic Genetics
language:en
Short-container-title:Ophthalmic Genetics

Author:

Chen Yan¹,Colville Deb¹,Ierino Francesco²,Symons Andrew³,Savige Judy¹

Affiliation:

1. Department of Medicine, Melbourne Health and Northern Health, The University of Melbourne, Melbourne, Australia

2. Department of Nephrology, Austin Health, Heidelberg, Heidelberg, Australia

3. Department of Ophthalmology and Surgery, Melbourne Health, Melbourne, Australia

Publisher

Informa UK Limited

Subject

Genetics (clinical),Ophthalmology,Pediatrics, Perinatology and Child Health

Link

https://www.tandfonline.com/doi/pdf/10.1080/13816810.2017.1401088

Reference26 articles.

1. Alport's syndrome

2. Genetic heterogeneity of Alport syndrome

3. Identification of Mutations in the COL4A5 Collagen Gene in Alport Syndrome

4. Identification of mutations in the α3(IV) and α4(IV) collagen genes in autosomal recessive Alport syndrome

5. Alport's Syndrome, Goodpasture's Syndrome, and Type IV Collagen

Cited by 16 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Characterization of Ocular Morphology in Col4a3^−/− Mice as a Murine Model for Alport Syndrome;Translational Vision Science & Technology;2024-07-23

2. Ocular manifestations of the genetic causes of focal and segmental glomerulosclerosis;Pediatric Nephrology;2023-08-14

3. Connective tissue disorders and eye: A review and recent updates;Indian Journal of Ophthalmology;2023-06

4. Heterozygous Pathogenic COL4A3 and COL4A4 Variants (Autosomal Dominant Alport Syndrome) Are Common, and Not Typically Associated With End-Stage Kidney Failure, Hearing Loss, or Ocular Abnormalities;Kidney International Reports;2022-09

5. Temporal retinal thinning might be an early diagnostic indicator in male pediatric X-linked Alport syndrome;International Journal of Ophthalmology;2022-07-18

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