The European Rare Disease Network for HHT Frameworks for management of hereditary haemorrhagic telangiectasia in general and speciality care

Author:

Shovlin C.L.,Buscarini E.,Sabbà C.,Mager H.J.,Kjeldsen A.D.,Pagella F.,Sure U.,Ugolini S.,Torring P.M.,Suppressa P.,Rennie C.,Post M.C.,Patel M.C.,Nielsen T.H.,Manfredi G.,Lenato G.M.,Lefroy D.,Kariholu U.,Jones B.,Fialla A.D.,Eker O.F.,Dupuis O.,Droege F.,Coote N.,Boccardi E.,Alsafi A.,Alicante S.,Dupuis-Girod S.

Funder

European Commission

Publisher

Elsevier BV

Subject

Genetics (clinical),Genetics,General Medicine

Reference53 articles.

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3. Cerebral abscess associated with odontogenic bacteremias, hypoxemia, and iron loading in immunocompetent patients with right-to-left shunting through pulmonary arteriovenous malformations;Boother;Clin. Infect. Dis.,2017

4. International similarities and differences in hereditary hemorrhagic telangiectasia (HHT) pathways reported by patients and clinicians;Boother;Thorax,2019

5. Safety of thalidomide and bevacizumab in patients with hereditary hemorrhagic telangiectasia;Buscarini;Orphanet J. Rare Dis.,2019

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