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Hereditary hemorrhagic teleangiectasia (Rendu-Osler-Weber disease).

Minerva cardioangiologica, 2002
Rendu-Osler-Weber disease, or hereditary hemorrhagic telangiectasia (HHT), is an autosomal dominant disorder with incomplete penetrance, characterized by vascular anomalies which may virtually develop in many organs. The prevalence varies and may range from 1/3,500 to 1/5,000 in specific regions.
SABBA', Carlo   +7 more
openaire   +1 more source

[Rendu-Osler-Weber syndrome and cerebral infarction].

Nederlands tijdschrift voor geneeskunde, 2010
A 30 year old man with a history of migraine presented at the neurology outpatient clinic with hypesthesia of the left side of his body during a migraine attack, which was unusual for him. His family history was positive for Rendu-Osler-Weber syndrome.
Aaike S, van den Berg   +4 more
openaire   +1 more source

Síndrome de Rendu-Osler-Weber

Medicina Clínica, 2019
Sonia Benítez-Rivero   +2 more
openaire   +1 more source

Hereditary Hemorrhagic Telangiectasis (Rendu-Osler-Weber Disease)

Optometry and Vision Science, 1981
T T, McMahon, J H, Maino
openaire   +2 more sources

[Rendu-Osler-Weber syndrome].

Ryoikibetsu shokogun shirizu, 1997
S, Tanabe, W, Koizumi, K, Saigenji
openaire   +1 more source

[Rendu-Osler-Weber disease].

Schweizerische medizinische Wochenschrift, 2000
N, Halkic   +3 more
openaire   +1 more source

Case report: Rendu-Osler-Weber syndrome

Journal of the American Academy of Dermatology, 2012
openaire   +1 more source

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