Results 171 to 180 of about 9,783 (206)

Hereditary Hemorrhagic Telangiectasia

Clinics in Chest Medicine, 2016
Hereditary hemorrhagic telangiectasia (HHT) is an underrecognized and underdiagnosed autosomal-dominant angiodysplasia that has an estimated prevalence of 1 in 5000 individuals, with variable clinical presentations even within family members with identical mutations.
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Hereditary Hemorrhagic Telangiectasia

New England Journal of Medicine, 1944
Karl Singer, William Q. Wolfson
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Hereditary hemorrhagic telangiectasia/avastin

The Laryngoscope, 2009
Abstract This is the first scientific report of hereditary hemorrhagic telangiectasia (HHT) epistaxis treatment by intranasal spraying of the vascular endothelial growth factor (VEGF) inhibitor bevacizumab (Avastin). Epistaxis in patients with HHT is a morbid, mortal condition that is difficult and unpleasant to manage.
Terence M, Davidson, Scott E, Olitsky, Julie L, Wei   +2 more
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Hereditary Hemorrhagic Telangiectasia

New England Journal of Medicine, 1932
RALPH C. LARRABEE, DAVID LITTMAN
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Hereditary Hemorrhagic Telangiectasia

Archives of Neurology, 1977
To the Editor.— The article entitled "Neurologic Aspects of Hereditary Hemorrhagic Telangiectasia" in the February issue of theArchives(34:101, 1977) prompts me to make the following comment. Approximately two years after the publication of my article 1 on the same subject (quoted in the above article), I had the opportunity to study the mother of ...
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Hereditary Hemorrhagic Telangiectasia and Gastrointestinal Hemorrhage

Gastroenterology, 1963
Summary In 1.59 patients with hereditary hemorrhagic telangiectasia, the chief manifestation of the disease was hemorrhage (89 per cent), with epistaxis being most common (81 per cent). The telangiectatic lesions were located primarily on the face, mucous membranes of the head, and hands.
C R, SMITH, L G, BARTHOLOMEW, J C, CAIN
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Hereditary Hemorrhagic Telangiectasia

New England Journal of Medicine, 1996
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Hereditary hemorrhagic telangiectasia.

The Annals of otology, rhinology, and laryngology, 2003
Hereditary hemorrhagic telangiectasia (HHT), also known as Osler-Weber-Rendu disease, is a rare disorder characterized by arteriovenous communications in visceral organs. The diagnosis of HHT consists of recurrent epistaxis, mucocutaneous telangiectasis, visceral vascular lesion and familial occurrence. HHT can be definitely diagnosed with the presence
D A, DOLOWITZ, O N, RAMBO, F E, STEPHENS
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Hemorrhagic hereditary telangiectasia

Gastrointestinal Endoscopy, 2006
Alberto Queiroz, Farias, Flair Jose, Carrilho   +1 more
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Hereditary Hemorrhagic Telangiectasia

Mayo Clinic Proceedings, 2007
Arif Hossain, Kamal, Udaya B S, Prakash
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