Antiplatelets and antithrombotics in neurointerventional procedures: Guideline update
CM Schirmer, KR Bulsara, F Al-Mufti… - Journal of …, 2023 - jnis.bmj.com
Background Antiplatelet and antithrombotic medication management before, during, and
after neurointerventional procedures has significant practice variation. This document …
after neurointerventional procedures has significant practice variation. This document …
Vascular anomaly syndromes in the ISSVA classification system: imaging findings and role of interventional radiology in management
Vascular anomalies encompass a spectrum of tumors and malformations that can cause
significant morbidity and mortality in children and adults. Use of the International Society for …
significant morbidity and mortality in children and adults. Use of the International Society for …
[HTML][HTML] The Role and Therapeutic Implications of Inflammation in the Pathogenesis of Brain Arteriovenous Malformations
Brain arteriovenous malformations (bAVMs) are focal vascular lesions composed of
abnormal vascular channels without an intervening capillary network. As a result, high …
abnormal vascular channels without an intervening capillary network. As a result, high …
[HTML][HTML] Imaging to intervention: a review of what the interventionalist needs to know about hereditary hemorrhagic telangiectasia
S Sobrepera, E Monroe, JJ Gemmete, D Hallam… - CVIR …, 2021 - Springer
Hereditary hemorrhagic telangiectasia (HHT) is a disorder that affects 1 in 5000–10,000
people worldwide and can result in devastating complications such as cerebral abscess …
people worldwide and can result in devastating complications such as cerebral abscess …
Unsupervised machine learning algorithms identify expected haemorrhage relationships but define unexplained coagulation profiles mapping to thrombotic …
G Mukhtar, CL Shovlin - EJHaem, 2023 - Wiley Online Library
Hereditary haemorrhagic telangiectasia (HHT) can result in challenging anaemia and
thrombosis phenotypes. Clinical presentations of HHT vary for relatives with identical casual …
thrombosis phenotypes. Clinical presentations of HHT vary for relatives with identical casual …
[HTML][HTML] Monogenic Causes of Cerebrovascular Disease in Childhood: A Case Series
BEL Ostrem, D Godfrey, PA Caruso, PL Musolino - Pediatric Neurology, 2023 - Elsevier
Background Despite an increase in the number of genes associated with pediatric stroke,
imaging phenotypes in children have not been well reported. Guidelines are needed to …
imaging phenotypes in children have not been well reported. Guidelines are needed to …
Current Practice: Rationale for Screening Children with Hereditary Hemorrhagic Telangiectasia for Brain Vascular Malformations
LA Beslow, AJ White, T Krings… - American Journal …, 2024 - Am Soc Neuroradiology
BACKGROUND: Hereditary hemorrhagic telangiectasia is an autosomal dominant vascular
dysplasia characterized by mucocutaneous telangiectasias, recurrent epistaxis, and organ …
dysplasia characterized by mucocutaneous telangiectasias, recurrent epistaxis, and organ …
Identifying racial disparities in hereditary hemorrhagic telangiectasia
H Yusuf, A Rasheed, H Kim, MB Conrad… - Journal of …, 2023 - jnis.bmj.com
Background Hereditary hemorrhagic telangiectasia (HHT) is a rare autosomal dominant
disorder characterized by recurrent epistaxis (nose bleeds), mucosal telangiectasias (spider …
disorder characterized by recurrent epistaxis (nose bleeds), mucosal telangiectasias (spider …
Hepatic vascular disorders: from diagnosis to interventional radiology
P Donato, J Facas, FC Alves - Seminars in Ultrasound, CT and MRI, 2022 - Elsevier
Hepatic vascular pathology comprises a spectrum of diseases with specific imaging features
that have portal hypertension as a common denominator. The imaging features of the main …
that have portal hypertension as a common denominator. The imaging features of the main …
[HTML][HTML] A case report of isolated right ventricular noncompaction with mutation of ACVRL1: a new cause of noncompaction of ventricular myocardium?
B Yu, K Shi, Y Wen, Y Yang - BMC Cardiovascular Disorders, 2023 - Springer
Background Noncompaction of ventricular myocardium (NVM) is a rare kind of
cardiomyopathy associated with genetic mutations and nongenetic factors, among which the …
cardiomyopathy associated with genetic mutations and nongenetic factors, among which the …