Ocular manifestations in hereditary hemorrhagic telangiectasia (Rendu-Osler-Weber disease): A case-series-Reference-Cited by-同舟云学术

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Ocular manifestations in hereditary hemorrhagic telangiectasia (Rendu-Osler-Weber disease): A case-series

Published:2010-12-21 Issue:1 Volume:32 Page:12-17
ISSN:1381-6810
Container-title:Ophthalmic Genetics
language:en
Short-container-title:Ophthalmic Genetics

Author:

Rinaldi Michele,Buscarini Elisabetta,Danesino Cesare,Chiosi Flavia,De Benedictis Antonella,Porcellini Antonio,Costagliola Ciro

Publisher

Informa UK Limited

Subject

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

Link

http://www.tandfonline.com/doi/pdf/10.3109/13816810.2010.535891

Reference31 articles.

1. A combined syndrome of juvenile polyposis and hereditary haemorrhagic telangiectasia associated with mutations in MADH4 ( SMAD4)

2. Genotype-phenotype relationship in hereditary haemorrhagic telangiectasia

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. Retinal telangiectasia-like lesions in a 15-year-old female with Hereditary hemorrhagic telangiectasia – a case report;BMC Ophthalmology;2022-11-07

2. An update on the ophthalmic features in hereditary haemorrhagic telangiectasia (Rendu-Osler-Weber syndrome);International Ophthalmology;2022-01-16

3. Ocular Manifestations of Neurocutaneous Syndromes;Neurocutaneous Disorders;2022

4. A Rare Coexistence of Isolated Unilateral Conjunctival Telangiectasia and Retinal Vascular Tortuosity;Case Reports in Ophthalmological Medicine;2020-08-24

5. Ocular lesions in hereditary hemorrhagic telangiectasia: genetics and clinical characteristics;Orphanet Journal of Rare Diseases;2020-06-29

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