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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2000 1
2002 1
2005 3
2006 2
2007 2
2008 2
2009 3
2010 1
2011 1
2012 2
2013 2
2014 4
2015 5
2016 3
2017 2
2018 2
2019 3
2020 3
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2022 4
2023 2
2024 2

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48 results

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Page 1
Genotype-Phenotype Correlations in Children with HHT.
Kilian A, Latino GA, White AJ, Clark D, Chakinala MM, Ratjen F, McDonald J, Whitehead K, Gossage JR, Lin D, Henderson K, Pollak J, McWilliams JP, Kim H, Lawton MT, Faughnan ME; the Brain Vascular Malformation Consortium HHT Investigator Group. Kilian A, et al. J Clin Med. 2020 Aug 22;9(9):2714. doi: 10.3390/jcm9092714. J Clin Med. 2020. PMID: 32842615 Free PMC article.
Neurovascular Complications and Pulmonary Arteriovenous Malformation Feeding Artery Size.
Ananiadis T, Faughnan ME, Clark D, Prabhudesai V, Kim H, Lawton MT, Vozoris NT; Brain Vascular Malformation Consortium HHT Investigator Group. Ananiadis T, et al. Ann Am Thorac Soc. 2022 Aug;19(8):1432-1435. doi: 10.1513/AnnalsATS.202202-130RL. Ann Am Thorac Soc. 2022. PMID: 35442860 Free PMC article. No abstract available.
Aspergillosis spores and medical marijuana.
Vethanayagam D, Saad E, Yehya J. Vethanayagam D, et al. CMAJ. 2016 Feb 16;188(3):217. doi: 10.1503/cmaj.1150081. CMAJ. 2016. PMID: 26883889 Free PMC article. No abstract available.
Quantification metrics for telangiectasia using optical coherence tomography.
Cardinell JL, Ramjist JM, Chen C, Shi W, Nguyen NQ, Yeretsian T, Choi M, Chen D, Clark DS, Curtis A, Kim H, Faughnan ME, Yang VXD; Brain Vascular Malformation Consortium HHT Investigator Group. Cardinell JL, et al. Sci Rep. 2022 Feb 2;12(1):1805. doi: 10.1038/s41598-022-05272-1. Sci Rep. 2022. PMID: 35110554 Free PMC article.
Predictors of mortality in patients with hereditary hemorrhagic telangiectasia.
Thompson KP, Nelson J, Kim H, Pawlikowska L, Marchuk DA, Lawton MT, Faughnan ME; Brain Vascular Malformation Consortium HHT Investigator Group. Thompson KP, et al. Orphanet J Rare Dis. 2021 Jan 6;16(1):12. doi: 10.1186/s13023-020-01579-2. Orphanet J Rare Dis. 2021. PMID: 33407668 Free PMC article.
Severity score for hereditary hemorrhagic telangiectasia.
Latino GA, Kim H, Nelson J, Pawlikowska L, Young W, Faughnan ME; Brain Vascular Malformation Consortium HHT Investigator Group. Latino GA, et al. Orphanet J Rare Dis. 2014 Dec 29;9:188. doi: 10.1186/s13023-014-0188-3. Orphanet J Rare Dis. 2014. PMID: 25928712 Free PMC article.
Sarcoidosis: a prospective observational cohort from Northern Alberta.
Vethanayagam D, Peters J, Saad E, Mulchey K, Gillson AM, McNab B, Farr-Jones M, Hruczkowski T, Blevins G, Coulden R, Oudit G, Beach J. Vethanayagam D, et al. Sarcoidosis Vasc Diffuse Lung Dis. 2020;37(4):e2020014. doi: 10.36141/svdld.v37i4.8522. Epub 2020 Dec 16. Sarcoidosis Vasc Diffuse Lung Dis. 2020. PMID: 33597801 Free PMC article.
48 results