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A retrospective cohort study on European Reference Network for Rare Vascular Diseases 5 outcome measures for Hereditary Haemorrhagic Telangiectasia in Denmark

BACKGROUND: Hereditary Haemorrhagic Telangiectasia (HHT) is an autosomal dominant disorder characterized by several clinical symptoms including epistaxis, arteriovenous malformations (AVM), and telangiectasia. In 2018, European Reference Network for Rare Vascular Diseases (VASCERN) recommended five...

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Detalles Bibliográficos
Autores principales:	Hvelplund, Troels, Lange, Bibi, Bird, Susanne Djernes, Korsholm, Malene, Kjeldsen, Anette Drøhse
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	BioMed Central 2022
Materias:	Research
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8734368/ https://www.ncbi.nlm.nih.gov/pubmed/34991676 http://dx.doi.org/10.1186/s13023-021-02160-1

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