Elevated FVIII levels in hereditary hemorrhagic telangiectasia: Implications for clinical management

Elevated FVIII levels in hereditary hemorrhagic telangiectasia: Implications for clinical management

Abstract Objectives The objective of this study was twofold: to determine the prevalence of arterial and venous thromboembolic events in the Norwegian Hereditary Hemorrhagic Telangiectasia (HHT) population, and to explore potential factors linked to such events, with particular emphasis on FVIII. Me...

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Autors principals: Ole Jakob Jørgensen, Johan Edvard Steineger, Andreas Hillarp, Erik Pareli Wåland, Pål André Holme, Ketil Heimdal, Sinan Dheyauldeen
Format: Article
Idioma:English
Publicat: Wiley 2024-02-01
Col·lecció:Laryngoscope Investigative Otolaryngology
Matèries:
FVIII
hereditary hemorrhagic telangiectasia
HHT
Osler
thrombosis
Accés en línia:https://doi.org/10.1002/lio2.1196

Internet

https://doi.org/10.1002/lio2.1196

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