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Anesthetic considerations in a cardiac surgical patient with Osler-Weber-Rendu disease
Journal of Cardiothoracic and Vascular Anesthesia, 19920 SLER-Weber-Rendu disease, otherwise known as hereditary hemorrhagic telangiectasia (HHT), is an autosomal-dominant disease with an incidence of 1-2 per 100,000 and a high penetrante. The homozygous trait causes a rapidly fatal disease,’ but the more common heterozygous trait causes a mild disease that usually presents in adulthood.
C, Radu, D L, Reich, R, Tamman
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Laparoscopic Findings in Hereditary Haemorrhagic Telangiectasia (Osler-Weber-Rendu Disease)
Endoscopy, 1984The laparoscopic findings observed in eight patients with hereditary haemorrhagic telangiectasia are reported. Clinical signs or laboratory data suggestive of liver involvement were present in all cases and constituted the main indication for laparoscopic examination.
J A, Solis-Herruzo +4 more
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Surgical Management of Life-Threatening Epistaxis in Osler-Weber-Rendu Disease
Annals of Plastic Surgery, 1995Hereditary hemorrhagic telangiectasia is a systemic disorder of blood vessels. It often leads to severe epistaxis that is refractory to conventional therapy. Three patients with severe epistaxis caused by hereditary hemorrhagic telangiectasia unresponsive to laser coagulation and to septal dermoplasty and requiring multiple transfusions underwent ...
E E, Rebeiz +3 more
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The Journal of the Association of Physicians of India, 2006
S K, Mahajan +4 more
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S K, Mahajan +4 more
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No shinkei geka. Neurological surgery, 1991
A 54 year-old man, who had a hereditary hemorrhagic telangiectasia (Osler-Weber-Rendu disease; O-W-R) accompanied by pulmonary arteriovenous fistulas (PAVFs) and congestive heart failure, developed seizure, right hemiparesis and dysphasia. A brain CT scan revealed a cystic lesion with perifocal edema in left frontoparietal lobe.
M, Higuchi +5 more
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A 54 year-old man, who had a hereditary hemorrhagic telangiectasia (Osler-Weber-Rendu disease; O-W-R) accompanied by pulmonary arteriovenous fistulas (PAVFs) and congestive heart failure, developed seizure, right hemiparesis and dysphasia. A brain CT scan revealed a cystic lesion with perifocal edema in left frontoparietal lobe.
M, Higuchi +5 more
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Hereditary Hemorrhagic Telangiectasia (Osler-Weber-Rendu Disease)
Archives of Internal Medicine, 1996Hereditary hemorrhagic telangiectasia (HHT), also known as Osler-Weber-Rendu disease, is a hereditary disorder leading to easily bleeding telangiectases on skin and mucosal surfaces, and it is associated with the presence of arteriovenous malformations (AVMs) in multiple organ systems. These AVMs may cause serious complications when they are located in
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Osler-Weber-Rendu disease: a six generation family.
Gaoxiong yi xue ke xue za zhi = The Kaohsiung journal of medical sciences, 1993A Taiwanese family, with at least nine members in six generations has been affected with Osler-Weber-Rendu disease, also known as hereditary hemorrhagic telangiectasia. It is an autosomal dominant familial disease which involves systemic subepithelial fibrovascular dysplasia and manifests with telangiectasia or angiomas of the face, the palms, or the ...
L H, Cheng, W J, Tsai
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Osler-Weber-Rendu disease: MR findings in the liver.
Journal of computer assisted tomography, 1989We report the magnetic resonance (MR) findings in the liver of a patient with known Osler-Weber-Rendu disease, a rare disorder characterized by arteriovenous malformations involving multiple organ systems. To the best of our knowledge, the MR findings in liver involvement have not been previously reported.
D G, Varma +4 more
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Clinical spectrum of hereditary hemorrhagic telangiectasia (Osler-Weber-Rendu disease)
The American Journal of Medicine, 1987Hereditary hemorrhagic telangiectasia (Osler-Weber-Rendu disease) is an autosomal dominant, systemic fibrovascular dysplasia in which telangiectases, arteriovenous malformations, and aneurysms may be widely distributed throughout the body vasculature.
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The radiologic presentation of Osler-Weber-Rendu disease of the liver.
The American journal of gastroenterology, 1994A case of Osler-Weber-Rendu disease with extensive hepatic arteriovenous fistulation is described in detail. Hemodynamic and imaging data indicated hepatic artery to hepatic vein shunting. Enhanced magnetic resonance imaging demonstrated the existence of arteriovenous fistulas by virtue of simultaneous enhancement of hepatic arteries and veins ...
K, Ouchi +5 more
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