References analysis of the Wikipedia article "Hereditary hemorrhagic telangiectasia" in the English version

doi.org

Govani FS, Shovlin CL (July 2009). "Hereditary haemorrhagic telangiectasia: a clinical and scientific review". European Journal of Human Genetics. 17 (7): 860–71. doi:10.1038/ejhg.2009.35. PMC 2986493. PMID 19337313.

Dupuis-Girod S, Bailly S, Plauchu H (March 2010). "Hereditary hemorrhagic telangiectasia (HHT): from molecular biology to patient care". J. Thromb. Haemost. 8 (7): 1447–56. doi:10.1111/j.1538-7836.2010.03860.x. PMID 20345718. S2CID 22470402.

Fuchizaki U, Miyamori H, Kitagawa S, Kaneko S, Kobayashi K (November 2003). "Hereditary haemorrhagic telangiectasia (Rendu–Osler–Weber disease)". Lancet. 362 (9394): 1490–4. doi:10.1016/S0140-6736(03)14696-X. PMID 14602446. S2CID 5304256.

Gossage JR, Kanj G (August 1998). "Pulmonary arteriovenous malformations. A state of the art review". Am. J. Respir. Crit. Care Med. 158 (2): 643–61. doi:10.1164/ajrccm.158.2.9711041. PMID 9700146. Archived from the original on 2010-08-19. Retrieved 2010-07-24.

Faughnan ME, Granton JT, Young LH (May 2009). "The pulmonary vascular complications of hereditary haemorrhagic telangiectasia". Eur. Respir. J. 33 (5): 1186–94. doi:10.1183/09031936.00061308. PMID 19407052.

Buscarini E, Plauchu H, Garcia Tsao G, et al. (November 2006). "Liver involvement in hereditary hemorrhagic telangiectasia: consensus recommendations". Liver Int. 26 (9): 1040–6. doi:10.1111/j.1478-3231.2006.01340.x. PMID 17032403.

Faughnan ME, Palda VA, Garcia-Tsao G, et al. (2011). "International guidelines for the diagnosis and management of hereditary hemorrhagic telangiectasia". Journal of Medical Genetics. 48 (2): 73–87. doi:10.1136/jmg.2009.069013. PMID 19553198. S2CID 18957466.

Abdalla SA, Letarte M (February 2006). "Hereditary haemorrhagic telangiectasia: current views on genetics and mechanisms of disease". Journal of Medical Genetics. 43 (2): 97–110. doi:10.1136/jmg.2005.030833. PMC 2603035. PMID 15879500.

McAllister KA, Grogg KM, Johnson DW, et al. (December 1994). "Endoglin, a TGF-beta binding protein of endothelial cells, is the gene for hereditary haemorrhagic telangiectasia type 1". Nat. Genet. 8 (4): 345–51. doi:10.1038/ng1294-345. hdl:1765/57953. PMID 7894484. S2CID 21623340.

Johnson DW, Berg JN, Baldwin MA, et al. (June 1996). "Mutations in the activin receptor-like kinase 1 gene in hereditary haemorrhagic telangiectasia type 2". Nat. Genet. 13 (2): 189–95. doi:10.1038/ng0696-189. PMID 8640225. S2CID 21379604.

Cole SG, Begbie ME, Wallace GM, Shovlin CL (2005). "A new locus for hereditary haemorrhagic telangiectasia (HHT3) maps to chromosome 5". Journal of Medical Genetics. 42 (7): 577–82. doi:10.1136/jmg.2004.028712. PMC 1736109. PMID 15994879.

Bayrak-Toydemir P, McDonald J, Akarsu N, et al. (2006). "A fourth locus for hereditary hemorrhagic telangiectasia maps to chromosome 7". American Journal of Medical Genetics. 140 (20): 2155–62. doi:10.1002/ajmg.a.31450. PMID 16969873. S2CID 7393654.

Gallione CJ, Repetto GM, Legius E, et al. (March 2004). "A combined syndrome of juvenile polyposis and hereditary haemorrhagic telangiectasia associated with mutations in MADH4 (SMAD4)". Lancet. 363 (9412): 852–9. doi:10.1016/S0140-6736(04)15732-2. PMID 15031030. S2CID 29539536.

Friedlander RM (June 2007). "Clinical practice. Arteriovenous malformations of the brain". N. Engl. J. Med. 356 (26): 2704–12. doi:10.1056/NEJMcp067192. PMID 17596605.

Shovlin CL, Guttmacher AE, Buscarini E, et al. (Mar 2000). "Diagnostic criteria for hereditary hemorrhagic telangiectasia (Rendu–Osler–Weber syndrome)". American Journal of Medical Genetics. 91 (1): 66–7. doi:10.1002/(SICI)1096-8628(20000306)91:1<66::AID-AJMG12>3.0.CO;2-P. PMID 10751092.

Geisthoff UW, Fiorella ML, Fiorella R (2006). "Treatment of recurrent epistaxis in HHT". Curr. Pharm. Des. 12 (10): 1237–42. doi:10.2174/138161206776361255. PMID 16611115.

Al-Samkari, Hanny; Kasthuri, Raj S.; Iyer, Vivek N.; Pishko, Allyson M.; Decker, Jake E.; Weiss, Clifford R.; Whitehead, Kevin J.; Conrad, Miles B.; Zumberg, Marc S.; Zhou, Jenny Y.; Parambil, Joseph; Marsh, Derek; Clancy, Marianne; Bradley, Lauren; Wisniewski, Lisa (2024-09-19). "Pomalidomide for Epistaxis in Hereditary Hemorrhagic Telangiectasia". New England Journal of Medicine. 391 (11): 1015–1027. doi:10.1056/NEJMoa2312749. ISSN 0028-4793. PMC 11412318. PMID 39292928.

Dupuis-Girod, Sophie; Ambrun, Alexis; Decullier, Evelyne; Fargeton, Anne-Emmanuelle; Roux, Adeline; Bréant, Valentine; Colombet, Bettina; Rivière, Sophie; Cartier, César; Lacombe, Pascal; Chinet, Thierry; Blivet, Sandra; Blondel, Jean-Hugues; Gilbert-Dussardier, Brigitte; Dufour, Xavier (2016-09-06). "Effect of Bevacizumab Nasal Spray on Epistaxis Duration in Hereditary Hemorrhagic Telangectasia: A Randomized Clinical Trial". JAMA. 316 (9): 934–942. doi:10.1001/jama.2016.11387. ISSN 0098-7484. PMID 27599328.

Saunders WH (1963). "Septal dermoplasty: a new operative procedure for control of nosebleeds in patients with hereditary hæmorrhagic telangiectasia". J. Laryngol. Otol. 77 (1): 69–76. doi:10.1017/S0022215100060382. PMID 13986828. S2CID 41411171.

Young A (May 1967). "Closure of the nostrils in atrophic rhinitis". J. Laryngol. Otol. 81 (5): 515–24. doi:10.1017/S0022215100067426. PMID 6024992. S2CID 45818218.

Cusumano, Lucas R.; Duckwiler, Gary R.; Roberts, Dustin G.; McWilliams, Justin P. (30 August 2019). "Treatment of Recurrent Pulmonary Arteriovenous Malformations: Comparison of Proximal Versus Distal Embolization Technique". CardioVascular and Interventional Radiology. 43 (1): 29–36. doi:10.1007/s00270-019-02328-0. PMID 31471718. S2CID 201675132.

Shovlin CL (2010). "Hereditary haemorrhagic telangiectasia: pathophysiology, diagnosis and treatment" (PDF). Blood Rev. 24 (6): 203–19. doi:10.1016/j.blre.2010.07.001. hdl:10044/1/22167. PMID 20870325.

Dupuis-Girod S, Ginon I, Saurin JC, Marion D, Guillot E, Decullier E, Roux A, Carette MF, Gilbert-Dussardier B, Hatron PY, Lacombe P, Lorcerie B, Rivière S, Corre R, Giraud S, Bailly S, Paintaud G, Ternant D, Valette PJ, Plauchu H, Faure F (2012). "Bevacizumab in patients with hereditary hemorrhagic telangiectasia and severe hepatic vascular malformations and high cardiac output". JAMA. 307 (9): 948–55. doi:10.1001/jama.2012.250. PMID 22396517.

Franchini M, Frattini F, Crestani S, Bonfanti C (2012). "Novel treatments for epistaxis in hereditary hemorrhagic telangiectasia: a systematic review of the clinical experience with thalidomide". J Thromb Thrombolysis. 36 (3): 355–7. doi:10.1007/s11239-012-0840-5. PMID 23143669. S2CID 33837604.

Lebrin F, Srun S, Raymond K, Martin S, van den Brink S, Freitas C, Bréant C, Mathivet T, Larrivée B, Thomas JL, Arthur HM, Westermann CJ, Disch F, Mager JJ, Snijder RJ, Eichmann A, Mummery CL (2010). "Thalidomide stimulates vessel maturation and reduces epistaxis in individuals with hereditary hemorrhagic telangiectasia". Nat Med. 16 (4): 420–8. doi:10.1038/nm.2131. PMID 20364125. S2CID 10649281.

Babington BG (1865). "Hereditary epistaxis". Lancet. 2 (2195): 362–363. doi:10.1016/S0140-6736(02)55197-7.

Legg W (1876). "A case of haemophilia complicated with multiple naevi". Lancet. 2 (2781): 856–7. doi:10.1016/S0140-6736(02)49594-3.

Weber FP (1907). "Multiple hereditary developmental angiomata (telangiectases) of the skin and mucous membranes associated with recurring haemorrhages". Lancet. 2 (4377): 160–162. doi:10.1016/S0140-6736(00)32590-9.

jamanetwork.com

nih.gov

pubmed.ncbi.nlm.nih.gov

Friedlander RM (June 2007). "Clinical practice. Arteriovenous malformations of the brain". N. Engl. J. Med. 356 (26): 2704–12. doi:10.1056/NEJMcp067192. PMID 17596605.

Geisthoff UW, Fiorella ML, Fiorella R (2006). "Treatment of recurrent epistaxis in HHT". Curr. Pharm. Des. 12 (10): 1237–42. doi:10.2174/138161206776361255. PMID 16611115.

Young A (May 1967). "Closure of the nostrils in atrophic rhinitis". J. Laryngol. Otol. 81 (5): 515–24. doi:10.1017/S0022215100067426. PMID 6024992. S2CID 45818218.

ncbi.nlm.nih.gov

semanticscholar.org

api.semanticscholar.org

Young A (May 1967). "Closure of the nostrils in atrophic rhinitis". J. Laryngol. Otol. 81 (5): 515–24. doi:10.1017/S0022215100067426. PMID 6024992. S2CID 45818218.

worldcat.org

search.worldcat.org

Hereditary hemorrhagic telangiectasia (English Wikipedia)

atsjournals.org

ajrccm.atsjournals.org

doi.org

eur.nl

repub.eur.nl

handle.net

hdl.handle.net

imperial.ac.uk

spiral.imperial.ac.uk

jamanetwork.com

nih.gov

pubmed.ncbi.nlm.nih.gov

ncbi.nlm.nih.gov

semanticscholar.org

api.semanticscholar.org

web.archive.org

worldcat.org

search.worldcat.org

zenodo.org