Absence of renal phenotype in hereditary haemorrhagic telangiectasia

Author:

Healy Lachlan12ORCID,Nicholls Kathleen23,Gibson Robert24,Stella Damien24,Bogwitz Michael12,Taylor Jessica1,Walsh Maie12,Donaldson Liz1,Winship Ingrid12

Affiliation:

1. Department of Genomic Medicine; Royal Melbourne Hospital; Melbourne Victoria Australia

2. Department of Medicine; The University of Melbourne; Melbourne Victoria Australia

3. Department of Nephrology; Royal Melbourne Hospital; Melbourne Victoria Australia

4. Department of Radiology; Royal Melbourne Hospital; Melbourne Victoria Australia

Publisher

Wiley

Subject

Internal Medicine

Reference20 articles.

1. Patients with hereditary hemorrhagic telangiectasia have increased plasma levels of vascular endothelial growth factor and transforming growth factor-beta1 as well as high ALK1 tissue expression;Sadick;Haematologica,2005

2. Hereditary hemorrhagic telangiectasia: an angiographic study of abdominal visceral angiodysplasias associated with gastrointestinal hemorrhage;Halpern;Radiology,1968

3. Asymptomatic microhematuria: an indication of hereditary hemorrhagic telangiectasia?;Di Gennaro;J Urol,2005

4. Renal arteriovenous malformation requiring surgery in Rendu-Osler-Weber disease (hereditary hemorrhagic telangiectasia);Ziani;J Urol,2000

5. Profuse intravesical hemorrhage caused by Rendu-Osler-Weber disease;Babushkina;Klin Med (Mosk),2000

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