High risk of ischaemic stroke amongst patients with hereditary haemorrhagic telangiectasia
MS Kofoed, PM Tørring, AA Christensen… - European Journal of …, 2024 - Wiley Online Library
Background and purpose Hereditary haemorrhagic telangiectasia (HHT) is a genetic
disease with fragile blood vessels and vascular malformations, potentially causing …
disease with fragile blood vessels and vascular malformations, potentially causing …
Cerebral abscesses among D anish patients with hereditary haemorrhagic telangiectasia
AD Kjeldsen, PM Tørring, H Nissen… - Acta Neurologica …, 2014 - Wiley Online Library
Background Hereditary haemorrhagic telangiectasia (HHT) is a dominantly inherited
disease characterized by a wide variety of clinical manifestations, including pulmonary …
disease characterized by a wide variety of clinical manifestations, including pulmonary …
Neurologic phenotype associated with hereditary haemorrhagic telangiectasia in a monocentric cohort of 154 patients
T Drouet, IP Muresan, B Maro, MF Carette… - 2012 - Am Heart Assoc
Introduction Hereditary haemorrhagic telangiectasia (HHT) is an autosomal dominant
disorder that leads to the formation of vascular malformations in mucocutaneous tissues …
disorder that leads to the formation of vascular malformations in mucocutaneous tissues …
Personalised stroke evaluation and management: tailoring individualised patient care for hereditary haemorrhagic telangiectasia
Z Park, R Dunston, T Ranasinghe - BMJ Case Reports CP, 2024 - casereports.bmj.com
Hereditary haemorrhagic telangiectasia (HHT) has an estimated prevalence of 1 in 5000–
8000 individuals globally with pulmonary arteriovenous malformations (PAVMs) affecting …
8000 individuals globally with pulmonary arteriovenous malformations (PAVMs) affecting …
Cerebrovascular and cardiovascular disease burden in patients with hereditary hemorrhagic telangiectasia
Introduction Hereditary hemorrhagic telangiectasia (HHT) is a rare genetic disease with
prevalence of approximately 1 in 5000–10,000. We evaluated the prevalence and …
prevalence of approximately 1 in 5000–10,000. We evaluated the prevalence and …
Should asymptomatic patients with hereditary haemorrhagic telangiectasia (HHT) be screened for cerebral vascular malformations? Data from 22 061 years of HHT …
AJ Easey, GMF Wallace, JMB Hughes… - Journal of Neurology …, 2003 - jnnp.bmj.com
Background: The frequency of haemorrhage in individuals with hereditary haemorrhagic
telangiectasia (HHT), 10% of whom will have cerebral arteriovenous (AV) malformations …
telangiectasia (HHT), 10% of whom will have cerebral arteriovenous (AV) malformations …
Neurologic complications in hereditary hemorrhagic telangiectasia with pulmonary arteriovenous malformations: a systematic review
J Agarwal, J LaBranche, S Dhillon… - Canadian Journal of …, 2023 - cambridge.org
Background: Hereditary hemorrhagic telangiectasia (HHT) is an autosomal dominant multi-
organ condition occurring with a 1 in 3800 prevalence in Alberta. This genetic disorder leads …
organ condition occurring with a 1 in 3800 prevalence in Alberta. This genetic disorder leads …
Hemorrhage rates from brain arteriovenous malformation in patients with hereditary hemorrhagic telangiectasia
H Kim, J Nelson, T Krings, KG Terbrugge… - Stroke, 2015 - Am Heart Assoc
Background and Purpose—Hereditary hemorrhagic telangiectasia (HHT) is a systemic
disease characterized by mucocutaneous telangiectasias, epistaxis, and arteriovenous …
disease characterized by mucocutaneous telangiectasias, epistaxis, and arteriovenous …
Neurologic conditions in Hereditary Hemorrhagic Telangiectasia with pulmonary arteriovenous malformations: Database study
Abstract RATIONALE/OBJECTIVE: Hereditary Hemorrhagic Telangiectasia (HHT) is an
autosomal dominant genetic disorder affecting vascular maturation, with a prevalence of 1 in …
autosomal dominant genetic disorder affecting vascular maturation, with a prevalence of 1 in …
Pulmonary arteriovenous malformations are associated with silent brain infarcts in hereditary hemorrhagic telangiectasia patients
W Brinjikji, DM Nasr, CP Wood, VN Iyer - Cerebrovascular Diseases, 2017 - karger.com
Background and Purpose: There is a high prevalence of right-to-left shunting pulmonary
arteriovenous malformations (PAVMs), which are stroke risk factors, in hereditary …
arteriovenous malformations (PAVMs), which are stroke risk factors, in hereditary …