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Page 1
Relative environmental and social disadvantage in patients with idiopathic pulmonary fibrosis.
Thorax. 2022 Dec;77(12):1237-1242. doi: 10.1136/thoraxjnl-2021-217652. Epub 2021 Dec 23.
Thorax. 2022.
PMID: 34949724
Perceptions of Genetic Testing: A Mixed-Methods Study of Patients with Pulmonary Fibrosis and Their First-Degree Relatives.
Grant-Orser A, Avitzur N, Morisset J, Fell CD, Johannson KA.
Grant-Orser A, et al. Among authors: avitzur n.
Ann Am Thorac Soc. 2022 Aug;19(8):1305-1312. doi: 10.1513/AnnalsATS.202111-1300OC.
Ann Am Thorac Soc. 2022.
PMID: 35584322
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Vitamin D deficiency promotes epithelial barrier dysfunction and intestinal inflammation.
Assa A, Vong L, Pinnell LJ, Avitzur N, Johnson-Henry KC, Sherman PM.
Assa A, et al. Among authors: avitzur n.
J Infect Dis. 2014 Oct 15;210(8):1296-305. doi: 10.1093/infdis/jiu235. Epub 2014 Apr 21.
J Infect Dis. 2014.
PMID: 24755435
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Vitamin D deficiency predisposes to adherent-invasive Escherichia coli-induced barrier dysfunction and experimental colonic injury.
Assa A, Vong L, Pinnell LJ, Rautava J, Avitzur N, Johnson-Henry KC, Sherman PM.
Assa A, et al. Among authors: avitzur n.
Inflamm Bowel Dis. 2015 Feb;21(2):297-306. doi: 10.1097/MIB.0000000000000282.
Inflamm Bowel Dis. 2015.
PMID: 25590952
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Combined hereditary and somatic mutations of replication error repair genes result in rapid onset of ultra-hypermutated cancers.
Shlien A, Campbell BB, de Borja R, Alexandrov LB, Merico D, Wedge D, Van Loo P, Tarpey PS, Coupland P, Behjati S, Pollett A, Lipman T, Heidari A, Deshmukh S, Avitzur N, Meier B, Gerstung M, Hong Y, Merino DM, Ramakrishna M, Remke M, Arnold R, Panigrahi GB, Thakkar NP, Hodel KP, Henninger EE, Göksenin AY, Bakry D, Charames GS, Druker H, Lerner-Ellis J, Mistry M, Dvir R, Grant R, Elhasid R, Farah R, Taylor GP, Nathan PC, Alexander S, Ben-Shachar S, Ling SC, Gallinger S, Constantini S, Dirks P, Huang A, Scherer SW, Grundy RG, Durno C, Aronson M, Gartner A, Meyn MS, Taylor MD, Pursell ZF, Pearson CE, Malkin D, Futreal PA, Stratton MR, Bouffet E, Hawkins C, Campbell PJ, Tabori U; Biallelic Mismatch Repair Deficiency Consortium.
Shlien A, et al. Among authors: avitzur n.
Nat Genet. 2015 Mar;47(3):257-62. doi: 10.1038/ng.3202. Epub 2015 Feb 2.
Nat Genet. 2015.
PMID: 25642631
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3D myocardial deformation analysis from cine MRI as a marker of amyloid protein burden in cardiac amyloidosis: validation versus T1 mapping.
Avitzur N, Satriano A, Afzal M, Narous M, Mikami Y, Hansen R, Dobko G, Flewitt J, Lydell CP, Howarth AG, Chow K, Fine NM, White JA.
Avitzur N, et al.
Int J Cardiovasc Imaging. 2018 Dec;34(12):1937-1946. doi: 10.1007/s10554-018-1410-5. Epub 2018 Jul 16.
Int J Cardiovasc Imaging. 2018.
PMID: 30014362
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