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Quality of life in patients with hereditary haemorrhagic telangiectasia (HHT).
Zarrabeitia R, Fariñas-Álvarez C, Santibáñez M, Señaris B, Fontalba A, Botella LM, Parra JA. Zarrabeitia R, et al. Among authors: botella lm. Health Qual Life Outcomes. 2017 Jan 23;15(1):19. doi: 10.1186/s12955-017-0586-z. Health Qual Life Outcomes. 2017. PMID: 28114930 Free PMC article.
The Role of Propranolol as a Repurposed Drug in Rare Vascular Diseases.
Cuesta AM, Gallardo-Vara E, Casado-Vela J, Recio-Poveda L, Botella LM, Albiñana V. Cuesta AM, et al. Among authors: botella lm. Int J Mol Sci. 2022 Apr 11;23(8):4217. doi: 10.3390/ijms23084217. Int J Mol Sci. 2022. PMID: 35457036 Free PMC article. Review.
Executive summary of the 12th HHT international scientific conference.
Andrejecsk JW, Hosman AE, Botella LM, Shovlin CL, Arthur HM, Dupuis-Girod S, Buscarini E, Hughes CCW, Lebrin F, Mummery CL, Post MC, Mager JJ. Andrejecsk JW, et al. Among authors: botella lm. Angiogenesis. 2018 Feb;21(1):169-181. doi: 10.1007/s10456-017-9585-2. Angiogenesis. 2018. PMID: 29147802 Free article.
European Reference Network for Rare Vascular Diseases (VASCERN): When and how to use intravenous bevacizumab in Hereditary Haemorrhagic Telangiectasia (HHT)?
Dupuis-Girod S, Shovlin CL, Kjeldsen AD, Mager HJ, Sabba C, Droege F, Fargeton AE, Fialla AD, Gandolfi S, Hermann R, Lenato GM, Manfredi G, Post MC, Rennie C, Suppressa P, Sure U; ePag group; Buscarini E. Dupuis-Girod S, et al. Eur J Med Genet. 2022 Oct;65(10):104575. doi: 10.1016/j.ejmg.2022.104575. Epub 2022 Aug 5. Eur J Med Genet. 2022. PMID: 35940549 Free article.
96 results