Results 151 to 160 of about 1,710,432 (184)
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ROTH SPOTS IN A RENDU–OSLER–WEBER SYNDROME
RETINAL Cases & Brief ReportsPurpose: The purpose of this study was to describe the molecular diagnosis and atypical ocular presentation of a patient who suffered for a Rendu–Osler–Weber syndrome associated with juvenile polyposis syndrome. Methods: This is a case report of a patient who underwent fundus ...
Thomas Ferreira de Moura +4 more
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Rendu-Osler-Weber syndrome: a current perspective on cerebral manifestations
Journal of Clinical Neuroscience, 1998Rendu-Osler-Weber syndrome (hereditary haemorrhagic telangiectasia) is a vascular dysplasia characterized by recurrent epistaxis, mucocutaneous telangiectasia and a family history of the disorder. Although rare, it may cause significant morbidity to healthy and young individuals.
M J, McDonald, B P, Brophy, C, Kneebone
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Pulmonary Arteriovenous Fistula in a Patient with Rendu-Osler-Weber Syndrome
Respiration, 2009Pulmonary arteriovenous fistula (PAVF) is an abnormal connection between pulmonary arteries and veins. Patients with PAVF may have the Rendu-Osler-Weber syndrome, a disease transmitted by autosomal dominant mechanisms. Here we describe a case of PAVF in a 56-year-old women, who was admitted to our department because of dyspnea, hemoptysis, and a mass ...
F, Marchesani +6 more
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Contact endoscopy of the nose in patients with Rendu–Osler–Weber syndrome
Auris Nasus Larynx, 2007Teleangiectases are the source of hemorrhage in many HHT patients. Most frequent site of bleeding is the nose and more than 90% of all individuals with HHT suffer from recurrent epistaxis. Despite all efforts, treatment of epistaxis in HHT continues to be a problem for many otorhinolaryngologists, who can alleviate recurrent nosebleeds by ...
B J, Folz, J A, Werner
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[Syndromes 14. Rendu-Osler-Weber disease].
Nederlands tijdschrift voor tandheelkunde, 2002The Rendu-Osler-Weber disease is due to an autosomal dominant disease with multiple telangiectasia in skin and mucosa. Recurrent bleeding of the nose is due to telangiectasia of the nasal mucosa. Haemorrhage of the oral mucosa also occurs. Extensive arteriovenous malformations can be present in lungs, liver and brain. Treatment of bleedings in the oral
J A, Baart, J M, van Hagen
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[Rendu-Osler-Weber syndrome and cerebral infarction].
Nederlands tijdschrift voor geneeskunde, 2010A 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
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Diagnostic criteria for hereditary hemorrhagic telangiectasia (Rendu-Osler-Weber syndrome)
American Journal of Medical Genetics, 2000Hereditary Hemorrhagic Telangiectasia (HHT) is easily recognized in individuals displaying the classical triad of epistaxis, telangiectasia, and a suitable family history, but the disease is more difficult to diagnosis in many patients. Serious consequences may result if visceral arteriovenous malformations, particularly in the pulmonary circulation ...
Shovlin, C L +7 more
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[Rendu-Osler-Weber syndrome--a complex systemic disease].
MMW Fortschritte der Medizin, 2004Hereditary hemorrhagic teleangiectasia (HHT or Rendu-Osler-Weber Syndrome) is an inherited autosomal dominant disorder of the vascular connective tissue. The resulting vascular malformations can occur in virtually any organ. Nosebleeds can massively impact on the quality of life of those afflicted. However, visceral manifestations are likely to be more
U W, Geisthoff +3 more
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Tracheobronchial Telangiectases in Rendu-Osler-Weber Syndrome
Journal of Bronchology, 1997Antoni Rosell +3 more
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