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Osler-Weber-Rendu syndrome with multiple angiographic findings
The British Journal of Radiology, 1972Hereditary haemorrhagic telangiectasia or the Osler-Weber-Rendu syndrome is a hereditary disease manifested by telangiectasia of the skin and mucous membranes resulting in repeated episodes of epistaxis. The angiographic findings have been mainly oriented towards the arteriovenous malformations found in the lung and brain (Alexander and Harrington ...
M N, Kinkhabwala +2 more
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[Pulmonary involvement in Osler-Weber-Rendu syndrome].
Harefuah, 2000Hereditary hemorrhagic telangiectasia (Osler-Weber-Rendu syndrome) is a group of autosomal dominant diseases with variable penetration, characterized by vascular malformations. Recently hereditary hemorrhagic telangiectasia has been found to be a phenotypic expression of mutations in genes located on chromosomes 9 and 12, and possibly of other genes ...
E, Bron-Harlev, B, Zeevi, B Z, Garty
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Osler-Weber-Rendu syndrome. Urologist's view.
Urology, 1975Two patients had hereditary hemorrhagic telangiectasia with hematuria. Characteristic telangiectasia was demonstrated in the bladder, prostate, and prostatic urethra of 1 patient; the other had a bladder tumor. Pathophysiologic aspects and treatment of the syndrome are discussed. Hematuria in patients with hereditary hemorrhagic telangiectasia demands
J M, De Cenzo +2 more
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Osler-Weber-Rendu syndrome: Case report
2015Osler–Weber–Rendu syndrome, also known as hereditary haemorrhagic telangiectasia (HHT), is a rare disorder of the fibrovascular tissue. It is an under-recognized disorder that results from multisystem vascular dysplasia. It is characterized by telangiectasias and arteriovenous malformations (AVMs) of skin, mucosa and viscera.
Akintayo, RO, Bojuwoye, MO
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Melena and Epistaxis: Osler-Weber-Rendu Syndrome
The American Journal of the Medical Sciences, 2010Huan-Lin, Chen +3 more
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