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23. Deficiency in hereditary hemorrhagic telangiectasia-associated Endoglin elicits hypoxia-driven heart failure in zebrafish. Lelièvre E; Bureau C; Bordat Y; Frétaud M; Langevin C; Jopling C; Kissa K Dis Model Mech; 2023 May; 16(5):. PubMed ID: 37264878 [TBL] [Abstract][Full Text] [Related]
24. ALK-1 mutations in liver transplanted patients with hereditary hemorrhagic telangiectasia. Argyriou L; Pfitzmann R; Wehner LE; Twelkemeyer S; Neuhaus P; Nayernia K; Engel W Liver Transpl; 2005 Sep; 11(9):1132-5. PubMed ID: 16123970 [TBL] [Abstract][Full Text] [Related]
25. MiR-205 is downregulated in hereditary hemorrhagic telangiectasia and impairs TGF-beta signaling pathways in endothelial cells. Tabruyn SP; Hansen S; Ojeda-Fernández ML; Bovy N; Zarrabeitia R; Recio-Poveda L; Bernabéu C; Martial JA; Botella LM; Struman I Angiogenesis; 2013 Oct; 16(4):877-87. PubMed ID: 23800974 [TBL] [Abstract][Full Text] [Related]
26. Altered endothelial gene expression associated with hereditary haemorrhagic telangiectasia. Thomas B; Eyries M; Montagne K; Martin S; Agrapart M; Simerman-François R; Letarte M; Soubrier F Eur J Clin Invest; 2007 Jul; 37(7):580-8. PubMed ID: 17576210 [TBL] [Abstract][Full Text] [Related]
27. Reduced endothelial secretion and plasma levels of transforming growth factor-beta1 in patients with hereditary hemorrhagic telangiectasia type 1. Letarte M; McDonald ML; Li C; Kathirkamathamby K; Vera S; Pece-Barbara N; Kumar S Cardiovasc Res; 2005 Oct; 68(1):155-64. PubMed ID: 15907823 [TBL] [Abstract][Full Text] [Related]
28. Two common endoglin mutations in families with hereditary hemorrhagic telangiectasia in the Netherlands Antilles: evidence for a founder effect. Gallione CJ; Scheessele EA; Reinhardt D; Duits AJ; Berg JN; Westermann CJ; Marchuk DA Hum Genet; 2000 Jul; 107(1):40-4. PubMed ID: 10982033 [TBL] [Abstract][Full Text] [Related]
29. Bazedoxifene, a new orphan drug for the treatment of bleeding in hereditary haemorrhagic telangiectasia. Zarrabeitia R; Ojeda-Fernandez L; Recio L; Bernabéu C; Parra JA; Albiñana V; Botella LM Thromb Haemost; 2016 Jun; 115(6):1167-77. PubMed ID: 26818701 [TBL] [Abstract][Full Text] [Related]
30. [Analysis of angiogenesis related proteins and its implication in type-2 hereditary hemorrhagic telangiectasia]. Peng HL; Hu GY; Zhang GS; Gong FJ Zhonghua Xue Ye Xue Za Zhi; 2006 Sep; 27(9):616-20. PubMed ID: 17278429 [TBL] [Abstract][Full Text] [Related]
36. Molecular and functional analysis identifies ALK-1 as the predominant cause of pulmonary hypertension related to hereditary haemorrhagic telangiectasia. Harrison RE; Flanagan JA; Sankelo M; Abdalla SA; Rowell J; Machado RD; Elliott CG; Robbins IM; Olschewski H; McLaughlin V; Gruenig E; Kermeen F; Halme M; Räisänen-Sokolowski A; Laitinen T; Morrell NW; Trembath RC J Med Genet; 2003 Dec; 40(12):865-71. PubMed ID: 14684682 [TBL] [Abstract][Full Text] [Related]
37. Detection of a significant association between mutations in the ACVRL1 gene and hepatic involvement in German patients with hereditary haemorrhagic telangiectasia. Brakensiek K; Frye-Boukhriss H; Mälzer M; Abramowicz M; Bahr MJ; von Beckerath N; Bergmann C; Caselitz M; Holinski-Feder E; Muschke P; Oexle K; Strobl-Wildemann G; Wolff G; El-Harith EA; Stuhrmann M Clin Genet; 2008 Aug; 74(2):171-7. PubMed ID: 18498373 [TBL] [Abstract][Full Text] [Related]
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40. [Liver involvement in hereditary haemorrhagic telangiectasia (Rendu-Osler-Weber disease). Report of one case and review of the literature]. Proux A; Tapiero S; Girszyn N; Levesque H; Marie I Rev Med Interne; 2007 Nov; 28(11):775-9. PubMed ID: 17624637 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]