Hereditary hemorrhagic telangiectasia (HHT) is an autosomal dominant genetic disorder
that presents with telangiectases in skin and mucosae, and arteriovenous malformations …

Vascular disorders of the liver, although affecting less than 5/10,000 patients, collectively
account for a number of rare conditions that represent an important health problem …

Background HHT is an autosomal dominant disease with an estimated prevalence of at least
1/5000 which can frequently be complicated by the presence of clinically significant …

Hereditary haemorrhagic telangiectasia is a rare systemic autosomal dominantly inherited
disorder of the fibrovascular tissue with a wide variety of clinical manifestations. Diagnosis is …

Abstract Computer Aided Diagnosis (CAD) systems can support physicians in classifying
different kinds of breast cancer, liver cancer and blood tumours also revealed by images …

Hereditary haemorrhagic telangiectasia (HHT) is an autosomal dominant inherited disorder
characterised by vascular malformations in predominantly the brain, liver and lungs …

OBJECTIVES: Hereditary haemorrhagic telangiectasia (HHT) is a rare autosomal dominant
disorder that can lead to neurological manifestations including strokes and cerebral …

Introduction and objective: Computer Aided Decision (CAD) systems based on Medical
Imaging could support radiologists in grading Hepatocellular carcinoma (HCC) by means of …

OBJECTIVE: Hereditary hemorrhagic telangiectasia (HHT) is a vascular disorder causing
mucocutaneous telangiectases and visceral arteriovenous malformations (AVMs) …

AIM To evaluated vascular dynamic processes in the liver of hereditary hemorrhagic
telangiectasia (HHT) patients by ultrasound (US) considering quantitative analytic methods …