Results 51 to 60 of about 294,742 (337)
Intracranial arteriovenous malformations
Intracranial arteriovenous malformations (AVM) are rare lesions that are often discovered fortuitously. They should be identified on CT scan and MRI before resorting to angiography; the latter is used to prepare the treatment. This article describes the various types of subpial or dural AVM and the specific characteristics that enable their ...
Xavier Barreau+3 more
openaire +2 more sources
The roles of endoglin gene in cerebrovascular diseases. [PDF]
Endoglin (ENG, also known as CD105) is a transforming growth factor β (TGFβ) associated receptor and is required for both vasculogenesis and angiogenesis.
Ma, Li, Su, Hua, Zhang, Rui, Zhu, Wan
core +2 more sources
Brain arteriovenous malformations [PDF]
nema
Stojanović Sanja+5 more
doaj +1 more source
Characterizing the Healthcare Utilization and Costs of Hereditary Hemorrhagic Telangiectasia
ABSTRACT Hereditary hemorrhagic telangiectasia (HHT) is the second‐most common inherited bleeding disorder worldwide, afflicting one in 4000–5000 people, and is the most morbid inherited bleeding disorder of women. HHT causes recurrent severe epistaxis, chronic gastrointestinal bleeding, heavy menstrual bleeding, and arteriovenous malformations in the ...
Hanny Al‐Samkari+5 more
wiley +1 more source
Cardiac Arteriovenous Malformation
![Figure][1] [![Graphic][3] ][3][![Graphic][4] ][4] A 31-year-old woman with anxiety was seen by her primary care physician for progressive fatigue. Her electrocardiogram showed a left axis deviation, but was otherwise unremarkable.
Sachin S. Parikh+2 more
openaire +3 more sources
Severe hepatic and pulmonary involvement in Rendu-Osler-Weber syndrome [PDF]
We report the case of a young woman with hereditary hemorrhagic telangiectasia (HHT) with severe liver involvement and pulmonary shunting. The medical imaging in this patient illustrates the severe shunting that can occur in these patients who often are ...
Geerts, Anja+4 more
core +3 more sources
ABSTRACT Hereditary hemorrhagic telangiectasia (HHT, Osler‐Weber‐Rendu disease) is the second most common inherited bleeding disorder worldwide, affecting approximately 1 in 5000 people. Development of disease‐modifying and efficacious hemostatic agents to treat HHT has finally begun after decades without such medical therapies.
Hanny Al‐Samkari+22 more
wiley +1 more source
This report describes a case of embolic myocardial infarction secondary to a pulmonary arteriovenous malformation. Pulmonary arteriovenous malformations are rare and mostly congenital and are inherited as an autosomal dominant disorder known as ...
Gabriel Sánchez-Fernández, MD+4 more
doaj
Patients with hepatic arteriovenous malformations rarely present with pulmonary hypertension. We report the case of a 3-month-old boy who developed severe pulmonary hypertension due to a hepatic arteriovenous malformation.
Naruhiko Murase+8 more
doaj +1 more source
Background Posterior fossa malformations are less common than supratentorial malformations, but hemorrhages in posterior fossa are more serious due to presence of vital structures within this region.
S. Vignesh+6 more
doaj +1 more source