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A murine model of hereditary hemorrhagic telangiectasia.
Bourdeau A, Dumont DJ, Letarte M. Bourdeau A, et al. J Clin Invest. 1999 Nov;104(10):1343-51. doi: 10.1172/JCI8088. J Clin Invest. 1999. PMID: 10562296 Free PMC article.
Age-dependent endothelial nitric oxide synthase uncoupling in pulmonary arteries of endoglin heterozygous mice.
Belik J, Jerkic M, McIntyre BA, Pan J, Leen J, Yu LX, Henkelman RM, Toporsian M, Letarte M. Belik J, et al. Am J Physiol Lung Cell Mol Physiol. 2009 Dec;297(6):L1170-8. doi: 10.1152/ajplung.00168.2009. Epub 2009 Oct 9. Am J Physiol Lung Cell Mol Physiol. 2009. PMID: 19820034
Umbilical vein and placental vessels from newborns with hereditary haemorrhagic telangiectasia type 1 genotype are normal despite reduced expression of endoglin.
Chan NL, Bourdeau A, Vera S, Abdalla S, Gross M, Wong J, Cymerman U, Paterson AD, Mullen B, Letarte M. Chan NL, et al. Placenta. 2004 Feb-Mar;25(2-3):208-17. doi: 10.1016/S0143-4004(03)00181-4. Placenta. 2004. PMID: 14972453
Screening for pulmonary and cerebral arteriovenous malformations in children with hereditary haemorrhagic telangiectasia.
Al-Saleh S, Mei-Zahav M, Faughnan ME, MacLusky IB, Carpenter S, Letarte M, Ratjen F. Al-Saleh S, et al. Eur Respir J. 2009 Oct;34(4):875-81. doi: 10.1183/09031936.00030009. Epub 2009 Apr 22. Eur Respir J. 2009. PMID: 19386691 Clinical Trial.
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. Thomas B, et al. Eur J Clin Invest. 2007 Jul;37(7):580-8. doi: 10.1111/j.1365-2362.2007.01824.x. Eur J Clin Invest. 2007. PMID: 17576210
Hereditary haemorrhagic telangiectasia: mutation detection, test sensitivity and novel mutations.
Prigoda NL, Savas S, Abdalla SA, Piovesan B, Rushlow D, Vandezande K, Zhang E, Ozcelik H, Gallie BL, Letarte M. Prigoda NL, et al. J Med Genet. 2006 Sep;43(9):722-8. doi: 10.1136/jmg.2006.042606. Epub 2006 May 11. J Med Genet. 2006. PMID: 16690726 Free PMC article.
No live individual homozygous for a novel endoglin mutation was found in a consanguineous Arab family with hereditary haemorrhagic telangiectasia.
Karabegovic A, Shinawi M, Cymerman U, Letarte M. Karabegovic A, et al. J Med Genet. 2004 Nov;41(11):e119. doi: 10.1136/jmg.2004.022079. J Med Genet. 2004. PMID: 15520401 Free PMC article. No abstract available.
Primary pulmonary hypertension in families with hereditary haemorrhagic telangiectasia.
Abdalla SA, Gallione CJ, Barst RJ, Horn EM, Knowles JA, Marchuk DA, Letarte M, Morse JH. Abdalla SA, et al. Eur Respir J. 2004 Mar;23(3):373-7. doi: 10.1183/09031936.04.00085504. Eur Respir J. 2004. PMID: 15065824
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