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73 results

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Minimal encephalopathy in hereditary hemorrhagic telangiectasia patients with portosystemic vascular malformations.
Villanueva B, Cañabate A, Torres-Iglesias R, Cerdà P, Gamundí E, Ordi Q, Alba E, Sanz-Astier LA, Iriarte A, Ribas J, Castellote J, Pintó X, Riera-Mestre A. Villanueva B, et al. Among authors: cerda p. Orphanet J Rare Dis. 2024 Dec 21;19(1):484. doi: 10.1186/s13023-024-03493-3. Orphanet J Rare Dis. 2024. PMID: 39709450 Free PMC article.
Gender differences in hereditary hemorrhagic telangiectasia severity.
Mora-Luján JM, Iriarte A, Alba E, Sánchez-Corral MA, Cerdà P, Cruellas F, Ordi Q, Corbella X, Ribas J, Castellote J, Riera-Mestre A. Mora-Luján JM, et al. Among authors: cerda p. Orphanet J Rare Dis. 2020 Mar 2;15(1):63. doi: 10.1186/s13023-020-1337-5. Orphanet J Rare Dis. 2020. PMID: 32122373 Free PMC article.
Adrenomedullin as a potential biomarker involved in patients with hereditary hemorrhagic telangiectasia.
Iriarte A, Ochoa-Callejero L, García-Sanmartín J, Cerdà P, Garrido P, Narro-Íñiguez J, Mora-Luján JM, Jucglà A, Sánchez-Corral MA, Cruellas F, Gamundi E, Ribas J, Castellote J, Viñals F, Martínez A, Riera-Mestre A. Iriarte A, et al. Among authors: cerda p. Eur J Intern Med. 2021 Jun;88:89-95. doi: 10.1016/j.ejim.2021.03.039. Epub 2021 Apr 20. Eur J Intern Med. 2021. PMID: 33888392 Free article.
Translational medicine in hereditary hemorrhagic telangiectasia.
Riera-Mestre A, Cerdà P, Iriarte A, Graupera M, Viñals F. Riera-Mestre A, et al. Among authors: cerda p. Eur J Intern Med. 2022 Jan;95:32-37. doi: 10.1016/j.ejim.2021.09.003. Epub 2021 Sep 16. Eur J Intern Med. 2022. PMID: 34538686 Free article. Review.
Natural history of patients with venous thromboembolism and hereditary hemorrhagic telangiectasia. Findings from the RIETE registry.
Riera-Mestre A, Mora-Luján JM, Trujillo-Santos J, Del Toro J, Nieto JA, Pedrajas JM, López-Reyes R, Soler S, Ballaz A, Cerdà P, Monreal M; RIETE Investigators. Riera-Mestre A, et al. Among authors: cerda p. Orphanet J Rare Dis. 2019 Aug 9;14(1):196. doi: 10.1186/s13023-019-1172-8. Orphanet J Rare Dis. 2019. PMID: 31399146 Free PMC article.
Current HHT genetic overview in Spain and its phenotypic correlation: data from RiHHTa registry.
Sánchez-Martínez R, Iriarte A, Mora-Luján JM, Patier JL, López-Wolf D, Ojeda A, Torralba MA, Juyol MC, Gil R, Añón S, Salazar-Mendiguchía J, Riera-Mestre A; RiHHTa Investigators of the Rare Diseases Working Group from the Spanish Society of Internal Medicine. Sánchez-Martínez R, et al. Orphanet J Rare Dis. 2020 Jun 5;15(1):138. doi: 10.1186/s13023-020-01422-8. Orphanet J Rare Dis. 2020. PMID: 32503579 Free PMC article.
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