Results 101 to 110 of about 11,240 (218)
Caractéristiques cliniques et parcours médical des patients atteints de la maladie de Rendu-Osler suivis au CHUV [PDF]
Objectifs : Les objectifs de ce travail ont consisté à décrire les caractéristiques cliniques et la prise en charge des patients atteints de maladie de Rendu-Osler (MRO) évalués par le réseau multidisciplinaire du CHUV, le parcours médical de ces
FRIGERIO, C.
core
Focal Spot, Spring/Summer 1980 [PDF]
https://digitalcommons.wustl.edu/focal_spot_archives/1026/thumbnail ...
core +1 more source
Congenital vascular malformations update [PDF]
Presently, there is controversy and misconception in the diagnosis and management of most congenital vascular malformations. The aim of this manuscript is to identify the current knowledge of these poorly understood and relatively uncommon pathologies ...
Albores Figueroa, Rosemberg +4 more
core
Accompanying Pulmonary Arteriovenous Malformation in Patient with Hydatidiform Mole: A Case Report
The most common site of metastasis in gestational trophoblastic disease (GTD) is the lung. To the best of our knowledge, arteriovenous malformations (AVMs) associated with pulmonary metastatic lesions are extremely rare in patients with GTD.
So Hyeon Bak +4 more
doaj +1 more source
Embolization of pulmonary AVMs: no consistent effect on pulmonary artery pressure [PDF]
Davies, RJ +4 more
core +1 more source
Incidental pulmonary arteriovenous malformation
Burcu Ancın +3 more
openaire +3 more sources
Can iron treatments aggravate epistaxis in some patients with hereditary hemorrhagic telangiectasia?
Objectives/Hypothesis To examine whether there is a rationale for iron treatments precipitating nosebleeds (epistaxis) in a subgroup of patients with hereditary hemorrhagic telangiectasia (HHT).
Anand +61 more
core +1 more source
Pulmonary arteriovenous malformations create continuous shunting of unoxygenated blood through the lungs into the systemic circulation. These malformations are asymptomatic if small, but cause serious symptoms as they grow in size.
Balazs C. Lengyel, MD +3 more
doaj +1 more source
Osler-Weber-Rendu Syndrome - Dental Implications [PDF]
Osler-Weber-Rendu syndrome (OWRS) is a rare hereditary, autosomal dominant disease characterized by a local angiodysplasia. Its clinical characteristics are vascular hamartomas of the skin and oral mucosa, arteriovenous malformations in the lungs, liver,
FERNANDES, Karin Sa +2 more
core
Pulmonary arteriovenous malformation
Padmanabhan Arjun +2 more
openaire +3 more sources

