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Second International Guidelines for the Diagnosis and Management of Hereditary Hemorrhagic Telangiectasia.
Ann Intern Med. 2020 Dec 15;173(12):989-1001. doi: 10.7326/M20-1443. Epub 2020 Sep 8.
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Intractable bleeding from the renal pelvis in a patient with hereditary haemorrhagic telangiectasia (Rendu-Osler-Weber disease).
Scand J Urol. 2020 Oct;54(5):449-451. doi: 10.1080/21681805.2020.1798505. Epub 2020 Jul 28.
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Absence of renal phenotype in hereditary haemorrhagic telangiectasia.
Intern Med J. 2018 Oct;48(10):1255-1257. doi: 10.1111/imj.14059.
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Hereditary hemorrhagic telangiectasia: genetics and molecular diagnostics in a new era.
Front Genet. 2015 Jan 26;6:1. doi: 10.3389/fgene.2015.00001. eCollection 2015.
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Management of renal arteriovenous malformations: A pictorial review.
Insights Imaging. 2014 Aug;5(4):523-30. doi: 10.1007/s13244-014-0342-4. Epub 2014 Jul 5.
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Endovascular treatment of a renal arteriovenous malformation with Onyx.
Cardiovasc Intervent Radiol. 2012 Feb;35(1):211-4. doi: 10.1007/s00270-011-0298-4.
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Diagnostic criteria for hereditary hemorrhagic telangiectasia (Rendu-Osler-Weber syndrome).
Am J Med Genet. 2000 Mar 6;91(1):66-7. doi: 10.1002/(sici)1096-8628(20000306)91:1<66::aid-ajmg12>3.0.co;2-p.

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