Results 61 to 70 of about 5,408,332 (199)

Variant distribution and characterization of hereditary hemorrhagic telangiectasia in Chinese patients

Eye &ENT Research, Volume 2, Issue 1, Page 53-61, March 2025.
Abstract Background Hereditary hemorrhagic telangiectasia (HHT) is an autosomal dominant disorder with variable manifestations, including recurrent epistaxis, telangiectasias, arteriovenous malformations, and family history. It is caused by heterozygous null alleles of ENG, ACVRL1, SMAD4, or BMP9, with delayed clinical diagnosis.
Yali Zhao, Xiangdong Wang, Yuhui Ouyang, Lin Xi, Yuan Zhang, Yan Zhao   +5 more
wiley   +1 more source

Osler-Weber-Rendu Syndrome [PDF]

, 2019
Yetmiş dört yaşındaki erkek olgu, yüzünde ve oral mukozada telenjiyektaziler ve sık burun kanaması şikâyetiyle polikliniğimize başvurdu. Olgunun öz geçmişinde, iki kere mide kanaması geçirdiği ve sık burun kanama öyküsü olduğu anlaşıldı.
An, İsa, İsa AN
core   +1 more source

Rendu-Osler-weber disease. Case report

, 2020
Rendu-Osler-Weber disease is the most frequently observed genetic hemorrhagic angiopathy with local wall thinning, distention of microcirculation vessels' lumen, and incomplete local hemostasis.
Kurochkin Sergei Vyacheslavovich, Gafurov Marat, Kurochkin S., Gafurov M., Zidikhanov Damir Ilshatovich, Chuvashaev I., Chuvashaev Iskander, Zidikhanov D.   +7 more
core  

Approach to anaemia in gastrointestinal disease: A position paper by the ESPGHAN Gastroenterology Committee

Journal of Pediatric Gastroenterology and Nutrition, Volume 80, Issue 3, Page 510-532, March 2025.
Approach to Anaemia in paediatric Gastrointestinal Disease Abstract Anaemia is a frequent consequence of many gastrointestinal (GI) diseases in children and it can even be the initial presenting symptom of underlying chronic GI disease. The definition of anaemia is age and gender‐dependent and it can be classified based on pathophysiology, red cell ...
Ilse Julia Broekaert, Amit Assa, Osvaldo Borrelli, Marco Deganello Saccomani, Matjaž Homan, Javier Martin‐de‐Carpi, Emmanuel Mas, Erasmo Miele, Zrinjka Misak, Sara Sila, Mike Thomson, Christos Tzivinikos, Jernej Dolinsek   +12 more
wiley   +1 more source

Life-threatening anaemia in patient with hereditary haemorrhagic telangiectasia (Rendu-Osler-Weber syndrome)

Open Medicine, 2020
Hereditary haemorrhagic telangiectasia (HHT), also known as Rendu-Osler-Weber syndrome, is a rare autosomal dominant vascular disorder. Patients with HHT may present with a wide spectrum of clinical manifestations from epistaxis to clinically significant
Mikołajczyk-Solińska Melania, Leończyk Karolina, Brzezina Aleksandra, Rossa Sylwia, Kasznicki Jacek   +4 more
doaj   +1 more source

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

A case of Osler-Weber-Rendu disease of the oral mucosa.

Japanese Journal of Oral & Maxillofacial Surgery, 1996
We report a case of Osler-Weber-Rendu disease occurring in the oral mucosa. A 56-year-old woman visited our clinic complaining of blood oozing from the oral mucosa. The patient had received treatment for anemia for about 30 years. The involvement of hereditary factors was suspected because of her grandfather, mother and two sisters had hemorrhagic ...
MASHIMO, Hajime, MUNEKAWA, Katsuhiko, TAKEDA, Gen-ichi   +2 more
openaire   +2 more sources

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