The many roles of tranexamic acid: an overview of the clinical indications for TXA in medical and surgical patients

J Cai, J Ribkoff, S Olson… - European journal of …, 2020 - Wiley Online Library
Clinically significant bleeding can occur as a consequence of surgery, trauma, obstetric
complications, anticoagulation, and a wide variety of disorders of hemostasis. As the causes …

The role of endoglin and its soluble form in pathogenesis of preeclampsia

G Margioula-Siarkou, C Margioula-Siarkou… - Molecular and Cellular …, 2022 - Springer
Preeclampsia remains till today a leading cause of maternal and fetal morbidity and
mortality. Pathophysiology of the disease is not yet fully elucidated, though it is evident that it …

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

H Al-Samkari, RS Kasthuri, JG Parambil… - …, 2021 - ncbi.nlm.nih.gov
Hereditary hemorrhagic telangiectasia (HHT, Osler-Weber-Rendu disease) is a rare
multisystem vascular disorder that causes chronic gastrointestinal bleeding, epistaxis, and …

Hereditary hemorrhagic telangiectasia: systemic therapies, guidelines, and an evolving standard of care

H Al-Samkari - Blood, The Journal of the American Society of …, 2021 - ashpublications.org
Hereditary hemorrhagic telangiectasia (HHT) management is evolving because of the
emergence and development of antiangiogenic therapies to eliminate bleeding …

Building the foundation for a community-generated national research blueprint for inherited bleeding disorders: research priorities for mucocutaneous bleeding …

RF Sidonio, Jr, PC Bryant, J Di Paola… - Expert Review of …, 2023 - Taylor & Francis
Background Excessive or abnormal mucocutaneous bleeding (MCB) may impact all aspects
of the physical and psychosocial wellbeing of those who live with it (PWMCB). The evidence …

[HTML][HTML] A precision medicine approach to hereditary hemorrhagic telangiectasia and complex vascular anomalies

H Al‐Samkari, W Eng - Journal of Thrombosis and Haemostasis, 2022 - Elsevier
Vascular anomalies represent a diverse group of disorders classified broadly as
malformations or tumors and include the second most common hereditary bleeding disorder …

uAUG creating variants in the 5'UTR of ENG causing Hereditary Hemorrhagic Telangiectasia

O Soukarieh, E Tillet, C Proust, C Dupont… - npj Genomic …, 2023 - nature.com
Abstract Hereditary Hemorrhagic Telangiectasia (HHT) is a rare, autosomal dominant,
vascular disorder. About 80% of cases are caused by pathogenic variants in ACVRL1 (also …

[HTML][HTML] Prevascularization techniques for dental pulp regeneration: potential cell sources, intercellular communication and construction strategies

Q Ruan, S Tan, L Guo, D Ma, J Wen - Frontiers in Bioengineering and …, 2023 - frontiersin.org
One of the difficulties of pulp regeneration is the rapid vascularization of transplanted
engineered tissue, which is crucial for the initial survival of the graft and subsequent pulp …

The vascular niche in next generation microphysiological systems

ML Ewald, YH Chen, AP Lee, CCW Hughes - Lab on a Chip, 2021 - pubs.rsc.org
In recent years, microphysiological system (MPS, also known as, organ-on-a-chip or tissue
chip) platforms have emerged with great promise to improve the predictive capacity of …

Systemic bevacizumab for the treatment of chronic bleeding in hereditary haemorrhagic telangiectasia

H Al‐Samkari, A Kritharis… - Journal of internal …, 2019 - Wiley Online Library
Background Hereditary haemorrhagic telangiectasia (HHT) is a rare hereditary multisystem
vascular disorder causing visceral arteriovenous malformations and mucocutaneous …