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- Tortora A, Riccioni ME, Gaetani E, Ojetti V, Holleran G, Gasbarrini A. Rendu-Osler-Weber disease: a gastroenterologist's perspective. Orphanet J Rare Dis. 2019, 7;14(1):130. doi: 10.1186/s13023-019-1107-4.
- Boehlen F, landis BN, spahr L et al. Maladie de Rendu-Osler-Weber : importance d’une prise en charge multidisciplinaire. Rev Med Suisse 2016 ; 12 : 1056-62
- Dupuis-Girod S, Bailly S, Plauchu H. Hereditary hemorrhagic telangiectasia : from molecular biology to patient care. J Thromb Haemost 2010;8:1447-56.
- Garcia-Tsao G. Liver involvement in hereditary hemorrhagic telangiectasia. J Hepatol 2007;46:499-507.
- Shovlin CL, Guttmacher AE, Buscarini E, et al. Diagnostic criteria for hereditary hemorrhagic telangiectasia (Rendu-Osler-Weber syndrome). Am J Med Genet 2000;91:66-7.
- Geisthoff UW, Nguyen HL, Röth A, Seyfert U. How to manage patients with hereditary haemorrhagic telangiectasia. Br J Haematol 2015;171:443-52.
- D upuis-Girod S, Chesnais AL, Ginon I, et al. Long-term outcome of patients with hereditary hemorrhagic telangiectasia and severe hepatic involvement after orthotopic liver transplantation : A single-center study. Liver Transpl 2010;16:340-7.
- Welle CL, Welch BT, Brinjikji W, et al. Abdominal manifestations of hereditary hemorrhagic telangiectasia: a series of 333 patients over 15 years. Cureus. 2018 Sep 14;10(9):e3305. doi: 10.7759/cureus.3305
- Kiyeng JC, Siika A, Koech C, Bloomfield GS. Definite hereditary hemorrhagic telangiectasia in a 60-year-old black Kenyan woman: a case report. J Med Case Rep. 2016 May 25;10(1):126. doi: 10.1186/s13256-016-0909-4.
- Ljaz HM, Lodhi MU, Chowdhury W, et al. Co-existing Gastrointestinal Hemorrhage and Deep Vein Thrombosis in a Patient with Hereditary Hemorrhagic Telangiectasia: Management Dilemma.. 2019 Jul;44(7):2384-2391. doi: 10.1007/s00261-019-01976-7.
References
Tortora A, Riccioni ME, Gaetani E, Ojetti V, Holleran G, Gasbarrini A. Rendu-Osler-Weber disease: a gastroenterologist's perspective. Orphanet J Rare Dis. 2019, 7;14(1):130. doi: 10.1186/s13023-019-1107-4.
Boehlen F, landis BN, spahr L et al. Maladie de Rendu-Osler-Weber : importance d’une prise en charge multidisciplinaire. Rev Med Suisse 2016 ; 12 : 1056-62
Dupuis-Girod S, Bailly S, Plauchu H. Hereditary hemorrhagic telangiectasia : from molecular biology to patient care. J Thromb Haemost 2010;8:1447-56.
Garcia-Tsao G. Liver involvement in hereditary hemorrhagic telangiectasia. J Hepatol 2007;46:499-507.
Shovlin CL, Guttmacher AE, Buscarini E, et al. Diagnostic criteria for hereditary hemorrhagic telangiectasia (Rendu-Osler-Weber syndrome). Am J Med Genet 2000;91:66-7.
Geisthoff UW, Nguyen HL, Röth A, Seyfert U. How to manage patients with hereditary haemorrhagic telangiectasia. Br J Haematol 2015;171:443-52.
D upuis-Girod S, Chesnais AL, Ginon I, et al. Long-term outcome of patients with hereditary hemorrhagic telangiectasia and severe hepatic involvement after orthotopic liver transplantation : A single-center study. Liver Transpl 2010;16:340-7.
Welle CL, Welch BT, Brinjikji W, et al. Abdominal manifestations of hereditary hemorrhagic telangiectasia: a series of 333 patients over 15 years. Cureus. 2018 Sep 14;10(9):e3305. doi: 10.7759/cureus.3305
Kiyeng JC, Siika A, Koech C, Bloomfield GS. Definite hereditary hemorrhagic telangiectasia in a 60-year-old black Kenyan woman: a case report. J Med Case Rep. 2016 May 25;10(1):126. doi: 10.1186/s13256-016-0909-4.
Ljaz HM, Lodhi MU, Chowdhury W, et al. Co-existing Gastrointestinal Hemorrhage and Deep Vein Thrombosis in a Patient with Hereditary Hemorrhagic Telangiectasia: Management Dilemma.. 2019 Jul;44(7):2384-2391. doi: 10.1007/s00261-019-01976-7.