Results 61 to 70 of about 5,408,282 (157)

Portal Hypertension—Noninvasive Multiparametric Ultrasound‐Based Criteria and Measurements

Portal Hypertension &Cirrhosis, Volume 4, Issue 1, Page 44-65, March 2025.
The review article discusses B‐mode ultrasound (US), color Doppler imaging, arterial Doppler indices, contrast‐enhanced ultrasound (CEUS), endoscopic ultrasound (EUS) and elastography methods in the diagnosis, grading and staging of portal hypertension.
Kathleen Möller, Riyad Abu El Hija, Xiaolong Qi, Christian Jenssen, Sven Mutze, Burkhard Möller, Benjamin Misselwitz, Christoph F. Dietrich   +7 more
wiley   +1 more source

From 78% oxygen saturation to 95% in 60 minutes: Osler-Weber-Rendu syndrome endovascular treatment

Advances in Interventional Cardiology, 2020
Pulmonary arteriovenous malformations (PAVMs) are abnormal communications between the pulmonary artery and pulmonary vein without an intervening capillary system.
Maciej Szmygin, Michał Sojka, Krzysztof Pyra, Tomasz Jargiełło   +3 more
doaj   +1 more source

Pulmonary vascular manifestations of hereditary haemorrhagic telangiectasia

Pulmonary Circulation, Volume 14, Issue 4, October 2024.
Abstract Hereditary haemorrhagic telangiectasia (HHT) is an autosomal dominant, multisystem disorder that manifests with a spectrum of disease including cardiopulmonary complications. HHT is characterised by aberrant signalling via the transforming growth factor β (TGFβ) pathway, with loss of vascular integrity, angiogenesis and vascular dysplasia. The
Sarah Cullivan, Barry Kevane, Brian McCullagh, Terry M. O'Connor, Robin Condliffe, Sean Gaine   +5 more
wiley   +1 more source

ChatGPT Generated Otorhinolaryngology Multiple‐Choice Questions: Quality, Psychometric Properties, and Suitability for Assessments

OTO Open, Volume 8, Issue 3, July–September 2024.
Abstract Objective To explore Chat Generative Pretrained Transformer's (ChatGPT's) capability to create multiple‐choice questions about otorhinolaryngology (ORL). Study Design Experimental question generation and exam simulation. Setting Tertiary academic center.
Cecilia Lotto, Sean C. Sheppard, Wilma Anschuetz, Daniel Stricker, Giulia Molinari, Sören Huwendiek, Lukas Anschuetz   +6 more
wiley   +1 more source

Successful liver transplantation for Rendu-Weber-Osler disease, a single centre experience.

, 2011
BACKROUNDS/PURPOSE: Hereditary hemorrhagic telangiectasia or Rendu-Weber-Osler is an autosomal dominant inherited disorder characterized by arteriovenous malformations and telangiectasia that may affect the nose, skin, lungs, brain and gastrointestinal ...
Philippe Wolf, J. Cinqualbre, Bernard Ellero, Murad Odeh, P. Wolf, PIARDI, Tullio, ODEH, MURAD, Maxime Audet, A. Saouli, Marie-Lorraine Woehl-Jaeglé, Anne-Catherine Saouli, Tullio Piardi, B. Ellero, M. Cag, Jacques Cinqualbre, M. Woehl Jaeglé, Murat Cag, M. Audet   +17 more
core   +1 more source

Coexistence of brain capillary telangiectasia and venous angioma: A case report and literature review

Clinical Case Reports, Volume 12, Issue 5, May 2024.
Key Clinical Message While Cerebral vascular malformations exhibit distinct clinical and radiographical features, rare instances of coexisting lesions occur. This case report sheds light on the rare coexistence of brain capillary telangiectasia and venous angioma in a patient presenting with a seizure attributed to frontal lobe bleeding.
Moaz O. Moursi, Anas Alsadi, Yousra Ali, Jouhar Kolleri, Tanweer Hussein   +4 more
wiley   +1 more source

Angiogenesis and hereditary hemorrhagic telangiectasia. Rendu-Osler-Weber disease

, 2001
To date much of the recent work on pathological angiogenesis has focused on inflammatory diseases, diabetes and cancer in particular. Hereditary hemorrhagic telangiectasia or Rendu-Osler-Weber disease provides an example of the genetic disorder of ...
Pasculli G, Rizzi Rita, Cirulli Anna, Gallitelli M, Specchia G, SABBA C, RIZZI R, Sabba' C, Liso Vincenzo, CIRULLI A, LISO V., SPECCHIA, GIORGINA   +11 more
core   +1 more source

A case report on osler-weber-rendu disease [PDF]

, 1970
Osler-Weber-Rendu disease, also known as hereditary hemorrhagic telangiectasia (HHT) is a rare autosomal dominant genetic disorder that leads to abnormal blood vessel formation in the skin, mucous membrane and in organs such as lungs, liver, and ...
Khan, Ameez S, Salih, Samah Muhammed
core   +1 more source

An international, multicenter study of intravenous bevacizumab for bleeding in hereditary hemorrhagic telangiectasia: the InHIBIT-Bleed study

Haematologica, 2020
Hereditary hemorrhagic telangiectasia (HHT, Osler-Weber-Rendu disease) is a rare multisystem vascular disorder causing chronic gastrointestinal bleeding, epistaxis, and severe anemia.
Hanny Al-Samkari, Raj S. Kasthuri, Joseph G. Parambil, Hasan A. Albitar, Yahya A. Almodallal, Carolina Vázquez, Marcelo M. Serra, Sophie Dupuis-Girod, Craig B. Wilsen, Justin P. McWilliams, Evan H. Fountain, James R. Gossage, Clifford R. Weiss, Muhammad A. Latif, Assaf Issachar, Meir Mei-Zahav, Mary E. Meek, Miles Conrad, Josanna Rodriguez-Lopez, David J. Kuter, Vivek N. Iyer   +20 more
doaj   +1 more source

High risk of ischaemic stroke amongst patients with hereditary haemorrhagic telangiectasia

European Journal of Neurology, Volume 31, Issue 2, February 2024.
Abstract Background and purpose Hereditary haemorrhagic telangiectasia (HHT) is a genetic disease with fragile blood vessels and vascular malformations, potentially causing neurological manifestations, including stroke and cerebral abscesses. The study aimed to investigate neurological manifestations in the Danish HHT database, focusing on pulmonary ...
Mikkel Seremet Kofoed, Pernille M. Tørring, Alex Alban Christensen, Bibi Lange, Anette Drøhse Kjeldsen, Troels Halfeld Nielsen   +5 more
wiley   +1 more source