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Tacrolimus as a Promising Drug for Epistaxis and Gastrointestinal Bleeding in HHT.
Álvarez-Hernández P, Patier JL, Marcos S, Gómez Del Olmo V, Lorente-Herraiz L, Recio-Poveda L, Botella LM, Viteri-Noël A, Albiñana V. Álvarez-Hernández P, et al. Among authors: botella lm. J Clin Med. 2023 Nov 29;12(23):7410. doi: 10.3390/jcm12237410. J Clin Med. 2023. PMID: 38068462 Free PMC article.
Mutation in Chek2 triggers von Hippel-Lindau hemangioblastoma growth.
Cabrera-Montes J, Aguirre DT, Viñas-López J, Lorente-Herraiz L, Recio-Poveda L, Albiñana V, Pérez-Pérez J, Botella LM, Cuesta AM. Cabrera-Montes J, et al. Among authors: botella lm. Acta Neurochir (Wien). 2023 Dec;165(12):4241-4251. doi: 10.1007/s00701-023-05825-x. Epub 2023 Oct 16. Acta Neurochir (Wien). 2023. PMID: 37843608 Free PMC 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.
A Novel Splicing Mutation in the ACVRL1/ALK1 Gene as a Cause of HHT2.
Errasti Díaz S, Peñalva M, Recio-Poveda L, Vilches S, Casado-Vela J, Pérez Pérez J, Botella LM, Albiñana V, Cuesta AM. Errasti Díaz S, et al. Among authors: botella lm. J Clin Med. 2022 May 28;11(11):3053. doi: 10.3390/jcm11113053. J Clin Med. 2022. PMID: 35683441 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.
CIBERER: Spanish national network for research on rare diseases: A highly productive collaborative initiative.
Luque J, Mendes I, Gómez B, Morte B, López de Heredia M, Herreras E, Corrochano V, Bueren J, Gallano P, Artuch R, Fillat C, Pérez-Jurado LA, Montoliu L, Carracedo Á, Millán JM, Webb SM, Palau F; CIBERER Network; Lapunzina P. Luque J, et al. Clin Genet. 2022 May;101(5-6):481-493. doi: 10.1111/cge.14113. Epub 2022 Feb 4. Clin Genet. 2022. PMID: 35060122 Free PMC article. Review.
96 results