Results 71 to 80 of about 5,408,332 (199)

Successful liver transplantation for Rendu-Weber-Osler disease, a single centre experience.

open access: yes, 2011
BACKROUNDS/PURPOSE: Hereditary hemorrhagic telangiectasia or Rendu-Weber-Osler is an autosomal dominant inherited disorder characterized by arteriovenous malformations and telangiectasia that may affect the nose, skin, lungs, brain and gastrointestinal ...
Philippe Wolf   +17 more
core   +1 more source

Coexistence of brain capillary telangiectasia and venous angioma: A case report and literature review

open access: yesClinical Case Reports, Volume 12, Issue 5, May 2024.
Key Clinical Message While Cerebral vascular malformations exhibit distinct clinical and radiographical features, rare instances of coexisting lesions occur. This case report sheds light on the rare coexistence of brain capillary telangiectasia and venous angioma in a patient presenting with a seizure attributed to frontal lobe bleeding.
Moaz O. Moursi   +4 more
wiley   +1 more source

Angiogenesis and hereditary hemorrhagic telangiectasia. Rendu-Osler-Weber disease

open access: yes, 2001
To date much of the recent work on pathological angiogenesis has focused on inflammatory diseases, diabetes and cancer in particular. Hereditary hemorrhagic telangiectasia or Rendu-Osler-Weber disease provides an example of the genetic disorder of ...
Pasculli G   +11 more
core   +1 more source

An international, multicenter study of intravenous bevacizumab for bleeding in hereditary hemorrhagic telangiectasia: the InHIBIT-Bleed study

open access: yesHaematologica, 2020
Hereditary hemorrhagic telangiectasia (HHT, Osler-Weber-Rendu disease) is a rare multisystem vascular disorder causing chronic gastrointestinal bleeding, epistaxis, and severe anemia.
Hanny Al-Samkari   +20 more
doaj   +1 more source

High risk of ischaemic stroke amongst patients with hereditary haemorrhagic telangiectasia

open access: yesEuropean Journal of Neurology, Volume 31, Issue 2, February 2024.
Abstract Background and purpose Hereditary haemorrhagic telangiectasia (HHT) is a genetic disease with fragile blood vessels and vascular malformations, potentially causing neurological manifestations, including stroke and cerebral abscesses. The study aimed to investigate neurological manifestations in the Danish HHT database, focusing on pulmonary ...
Mikkel Seremet Kofoed   +5 more
wiley   +1 more source

Endoglin mutants retained in the endoplasmic reticulum exacerbate loss of function in hereditary hemorrhagic telangiectasia type 1 (HHT1) by exerting dominant negative effects on the wild type allele

open access: yesTraffic, Volume 25, Issue 1, January 2024.
The formation of heterodimers between ER‐retained endoglin mutants and WT endoglin impairs WT maturation and trafficking to the plasma membrane. Abstract Hereditary hemorrhagic telangiectasia (HHT) is an autosomal dominant disorder affecting 1 in 5000–8000 individuals.
Nesrin Gariballa   +2 more
wiley   +1 more source

Síndrome de Osler-Weber-Rendu

open access: yes, 2009
Tres imágenes de un síndrome de Osler-Weber-Rendu.Three pictures of a Osler-Weber-Rendu ...
Iglesias Rozas, José Rafael, 1942-
core  

Osler Weber Rendu Disease ( A Case Report)

open access: yesEurasian Journal of Medicine, 2019
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Nihat Okçu   +3 more
doaj  

Osler-Weber-Rendu sendromu ile ilişkili pulmoner arteriyovenöz malformasyon

open access: yes, 2011
Osler-Weber-Rendu syndrome is a relatively common vascular displasia of children presented with telengiectasias of skin, mucosa, and visceral organs and arteriovenous malformations.
Aygün Dindar   +5 more
core   +1 more source

PREGNANCY AND HERITABLE CONNECTIVE TISSUE DISORDERS (MARFAN SYNDROME, EHLERS DANLOS SYNDROME, OSLER-WEBER-RENDU DISEASE)

open access: yesАкушерство, гинекология и репродукция, 2016
The article describes some inherited disorders (Marfan syndrome, Ehlers-Danlos syndrome, Osler-Weber-Rendu disease) that affects the connective tissue with prominent manifestations in the skeletal, ocular, and cardiovascular systems during the pregnancy.
L. S. Radetskaya
doaj   +1 more source

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