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Second International Guidelines for the Diagnosis and Management of Hereditary Hemorrhagic Telangiectasia.
Faughnan ME, Mager JJ, Hetts SW, Palda VA, Lang-Robertson K, Buscarini E, Deslandres E, Kasthuri RS, Lausman A, Poetker D, Ratjen F, Chesnutt MS, Clancy M, Whitehead KJ, Al-Samkari H, Chakinala M, Conrad M, Cortes D, Crocione C, Darling J, de Gussem E, Derksen C, Dupuis-Girod S, Foy P, Geisthoff U, Gossage JR, Hammill A, Heimdal K, Henderson K, Iyer VN, Kjeldsen AD, Komiyama M, Korenblatt K, McDonald J, McMahon J, McWilliams J, Meek ME, Mei-Zahav M, Olitsky S, Palmer S, Pantalone R, Piccirillo JF, Plahn B, Porteous MEM, Post MC, Radovanovic I, Rochon PJ, Rodriguez-Lopez J, Sabba C, Serra M, Shovlin C, Sprecher D, White AJ, Winship I, Zarrabeitia R. Faughnan ME, et al. Among authors: henderson k. Ann Intern Med. 2020 Dec 15;173(12):989-1001. doi: 10.7326/M20-1443. Epub 2020 Sep 8. Ann Intern Med. 2020. PMID: 32894695 Free 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.
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. Among authors: henderson k. J Clin Med. 2020 Aug 22;9(9):2714. doi: 10.3390/jcm9092714. J Clin Med. 2020. PMID: 32842615 Free PMC article.
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.
Overlapping spectra of SMAD4 mutations in juvenile polyposis (JP) and JP-HHT syndrome.
Gallione C, Aylsworth AS, Beis J, Berk T, Bernhardt B, Clark RD, Clericuzio C, Danesino C, Drautz J, Fahl J, Fan Z, Faughnan ME, Ganguly A, Garvie J, Henderson K, Kini U, Leedom T, Ludman M, Lux A, Maisenbacher M, Mazzucco S, Olivieri C, Ploos van Amstel JK, Prigoda-Lee N, Pyeritz RE, Reardon W, Vandezande K, Waldman JD, White RI Jr, Williams CA, Marchuk DA. Gallione C, et al. Among authors: henderson k. Am J Med Genet A. 2010 Feb;152A(2):333-9. doi: 10.1002/ajmg.a.33206. Am J Med Genet A. 2010. PMID: 20101697
Pulmonary Hypertension Prevalence and Prognosis in a Cohort of Patients with Hereditary Hemorrhagic Telangiectasia Undergoing Embolization of Pulmonary Arteriovenous Malformations.
Chizinga M, Rudkovskaia AA, Henderson K, Pollak J, Garcia-Tsao G, Young LH, Fares WH. Chizinga M, et al. Among authors: henderson k. Am J Respir Crit Care Med. 2017 Nov 15;196(10):1353-1356. doi: 10.1164/rccm.201702-0267LE. Am J Respir Crit Care Med. 2017. PMID: 28375020 No abstract available.
SARS-CoV-2 Surveillance of Wild Mice and Rats in North American Cities.
Lee LKF, Himsworth CG, Prystajecky N, Dibernardo A, Lindsay LR, Albers TM, Dhawan R, Henderson K, Mulder G, Atwal HK, Beattie I, Wobeser BK, Parsons MH, Byers KA. Lee LKF, et al. Among authors: henderson k. Ecohealth. 2024 Mar;21(1):1-8. doi: 10.1007/s10393-024-01679-6. Epub 2024 May 15. Ecohealth. 2024. PMID: 38748281
1,022 results