Results 41 to 50 of about 177,116 (201)
Pericytes as targets in hereditary hemorrhagic telangiectasia [PDF]
Frontiers in Genetics, 2015 Defective paracrine Transforming Growth Factor-β (TGF-β) signaling between endothelial cells and the neighboring mural cells have been thought to lead to the development of vascular lesions that are characteristic of Hereditary Hemorrhagic Telangiectasia (HHT). This review highlights recent progress in our understanding of TGF-β signaling in mural cell
Thalgott, Jérémy +2 more
openaire +3 more sources
Hereditary Hemorrhagic Telangiectasia (Osler–Weber–Rendu Disease) [PDF]
, 2013 Angiectasias are the most frequent lesions in the small bowel. However, hereditary hemorrhagic telangiectasia is a rare condition diagnosed by genetic testing or clinical criteria (family history, recurrent epistaxis, telangiectasia, and visceral ...
Matsui, U +4 more
core +1 more source
Closure of the nasal cavities in the treatment of refractory hereditary haemorrhagic telangiectasia [PDF]
, 1997 From a cohort of 35 patients with hereditary haemorrhagic telangiectasia (HHT), 12 patients have undergone closure of the one or both nasal cavities during the last three years for refractory epistaxis.
Howard, DJ, Lund, VJ
core
B-ENT, 2022 Objective: Hereditary hemorrhagic telangiectasia, or Rendu-Osler-Weber disease, is an autosomal dominant genetic disorder characterized by abnormal vessel formation. Otorhinolaryngologists often struggle with recurrent epistaxis caused by telangiectasias
Fíková Alžběta +2 more
doaj +2 more sources
Osler-Weber-Rendu Disease Uncovered by Preeclampsia in a Case Report
Case Reports in Obstetrics and Gynecology, 2020 Osler-Weber-Rendu disease (OWRD), called hereditary hemorrhagic telangiectasia, is an uncommon genetic illness with the dominant autosomal transmission.
Jamal Ouachaou +7 more
doaj +1 more source
Journal of Pediatric Gastroenterology and Nutrition, EarlyView.Abstract Objectives Hereditary polyposis syndromes in children are rare, heterogeneous disorders associated with significant morbidity and long‐term risk of malignancy. Current data on their presentation, management, and outcomes in pediatric populations remain limited.
Shlomi Cohen +9 more
wiley +1 more source
Nail Disorders in Systemic Conditions
JEADV Clinical Practice, EarlyView.ABSTRACT Nail findings in children can be indicative of an underlying systemic disease. Many of these findings are seen in multiple entities and are not specific to one disease. The importance of specifically examining for these nail changes cannot be overstated.
Jane Sanders Bellet
wiley +1 more source
Lasers in Surgery and Medicine, EarlyView.ABSTRACT Objectives This exploratory pilot study aims to characterize effective laser settings and evaluate the clinical outcomes and tolerability of a dual‐wavelength 532/1064‐nm KTP/Nd: YAG laser system compared to a 595‐nm pulsed dye laser with cryogen spray cooling, across multiple vascular indications, including port‐wine capillary malformations ...
Olamide Sonuga Finney +5 more
wiley +1 more source
Interventional oncology in children: Where are we now?
Journal of Medical Imaging and Radiation Oncology, EarlyView.Abstract Paediatric Interventional Oncology (IO) lags behind adult IO due to a scarcity of specific outcome data. The suboptimal way to evolve this field is relying heavily on adult experiences. The distinct tumour types prevalent in children, such as extracranial germ cell tumours, sarcomas, and neuroblastoma, differ strongly from those found in ...
Premal Amrishkumar Patel +1 more
wiley +1 more source
Journal of Medical Case Reports, 2022 Background Hereditary hemorrhagic telangiectasia, also known as Osler–Weber–Rendu disease, induces arteriovenous malformations in visceral organs. Arteriovenous malformations increase the risk of severe infections and are a common complication associated
Genki Naruse +2 more
doaj +1 more source