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Page 1
Compelling reasons to screen brain in HHT.
Mandzia J, Henderson K, Faughnan M, White R Jr. Mandzia J, et al. Stroke. 2001 Dec 1;32(12):2957-8. Stroke. 2001. PMID: 11740006 No abstract available.
What is a good decision?
Ratliff A, Angell M, Dow RW, Kuppermann M, Nease RF Jr, Fisher R, Fisher ES, Redelmeier DA, Faughnan ME, Rimer BK, Pauker SP, Pauker SG, Sox HC. Ratliff A, et al. Among authors: faughnan me. Eff Clin Pract. 1999 Jul-Aug;2(4):185-97. Eff Clin Pract. 1999. PMID: 10539545 No abstract available.
The ACVRL1 c.314-35A>G polymorphism is associated with organ vascular malformations in hereditary hemorrhagic telangiectasia patients with ENG mutations, but not in patients with ACVRL1 mutations.
Pawlikowska L, Nelson J, Guo DE, McCulloch CE, Lawton MT, Young WL, Kim H, Faughnan ME; Brain Vascular Malformation Consortium HHT Investigator Group. Pawlikowska L, et al. Among authors: faughnan me. Am J Med Genet A. 2015 Jun;167(6):1262-7. doi: 10.1002/ajmg.a.36936. Epub 2015 Apr 2. Am J Med Genet A. 2015. PMID: 25847705 Free PMC article.
127 results