[HTML][HTML] Ischemic cholangitis: Lethal complication of Osler-Weber-Rendu disease
O Elmqaddem, H Koulali, A Zazour, M Nasiri… - Radiology Case …, 2024 - Elsevier
Abstract Osler-Weber-Rendu disease (OWRD), also known as hereditary haemorrhagic
telangiectasia (HHT), is an autosomal dominant genetic disorder characterised by …
telangiectasia (HHT), is an autosomal dominant genetic disorder characterised by …
[HTML][HTML] Multifocal Abscesses, Necrotizing Fasciitis, Iron Deficiency Anemia, and Hypophosphatemia Induced by Ferric Carboxymaltose Infusions: Report of a Case of …
LA Trevise, MPLV Pinto, G Hasselmann… - Cureus, 2023 - ncbi.nlm.nih.gov
Hereditary hemorrhagic telangiectasia (HHT) is a rare autosomal dominant vascular
dysplasia in which disrupted angiogenesis leads to increased formation of mucocutaneous …
dysplasia in which disrupted angiogenesis leads to increased formation of mucocutaneous …
La maladie de Rendu-Osler (télangiectasie hémorragique héréditaire)
A Parrot, M Barral, X Amiot, C Bachmeyer… - Revue des Maladies …, 2023 - Elsevier
Résumé La maladie de Rendu-Osler (MRO) est une maladie vasculaire du capillaire,
héréditaire autosomique dominante, rare, avec une prévalence de 1/5000. Elle est …
héréditaire autosomique dominante, rare, avec une prévalence de 1/5000. Elle est …
[PDF][PDF] Allogeneic hematopoietic stem cell transplantation for acute lymphoblastic leukemia with an accompanying hereditary hemorrhagic telangiectasia
D Habraszka, S Gawęda, A Spałek… - Acta Haematologica …, 2024 - journals.viamedica.pl
Rendu-Osler-Weber disease also known as hereditary hemorrhagic telangiectasia (HHT) is
a rare autosomal dominant disorder [1]. It is caused by mutations in the ENG, ACVRL1 or …
a rare autosomal dominant disorder [1]. It is caused by mutations in the ENG, ACVRL1 or …
Recurrent Paradoxical Embolism and Manganese Deposition in the Basal Ganglia in a Patient with Hereditary Haemorrhagic Telangiectasias: A Case Report and …
Q Tang, P Xia, X Hu, Y Shao - 2023 - researchsquare.com
Background Hereditary hemorrhagic telangiectasia (HHT) is a rare autosomal dominant
inherited vascular disorder that can involve multiple organs, thus can be associated with so …
inherited vascular disorder that can involve multiple organs, thus can be associated with so …
A Twin Pregnancy With Undiagnosed Hereditary Hemorrhagic Telangiectasia With Severe Hypoxia
JHC Wu, EC Lampley - Journal of Clinical Gynecology and Obstetrics, 2024 - jcgo.org
During pregnancies with hereditary hemorrhagic telangiectasia (HHT), rare severe
complications could be fatal. This study presents a Chinese immigrant with twin gestation …
complications could be fatal. This study presents a Chinese immigrant with twin gestation …
Unravelling the Mechanisms Regulating Endothelial Cell Size and Number to Control Blood Vessel Diameters
Z Diwan - 2023 - search.proquest.com
Aberrations in blood vessel diameters can disrupt hierarchical vascular patterning and
cause severe congenital vascular anomalies, like arteriovenous malformations (AVMs) and …
cause severe congenital vascular anomalies, like arteriovenous malformations (AVMs) and …
Vaikų migrena. Literatūros apžvalga ir atvejo aprašymas (Osler-Weber-Rendu sindromas)
K Sabūnaitė - 2023 - epublications.vu.lt
Abstract [eng] Headache is a common condition among children, adolescents and young
adults that can have negative consequences for quality of life, social activity and even …
adults that can have negative consequences for quality of life, social activity and even …
Hemoraginė paveldima telangiektazija otorinolaringologijoje: etiopatogenezė, diagnostika ir gydymas
T Kavaliauskaitė - 2023 - epublications.vu.lt
Abstract [eng] Hereditary hemorrhagic telangiectasia is an autosomal dominant disorder
associated with alterations of angiogenesis. Heterozygous mutations in the ENG or ACVRL1 …
associated with alterations of angiogenesis. Heterozygous mutations in the ENG or ACVRL1 …
Malformação arteriovenosa mimetizando massa pulmonar em idoso: Relato de caso
MCB Lopes, MSM Fonseca… - Brazilian Journal of …, 2023 - ojs.brazilianjournals.com.br
A malformação arteriovenosa pulmonar é uma condição anômala em que há a
comunicação entre artéria e veia pulmonares ocasionando a formação de shunts da direita …
comunicação entre artéria e veia pulmonares ocasionando a formação de shunts da direita …