Results 71 to 80 of about 5,408,332 (199)
Successful liver transplantation for Rendu-Weber-Osler disease, a single centre experience.
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
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
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
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
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
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
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)
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Nihat Okçu +3 more
doaj
Osler-Weber-Rendu sendromu ile ilişkili pulmoner arteriyovenöz malformasyon
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
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

