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

Year Number of Results
2003 2
2005 1
2007 4
2009 2
2010 3
2011 3
2012 2
2013 3
2014 2
2015 1
2016 5
2017 3
2018 2
2019 3
2020 5
2021 2
2022 1
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40 results
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Page 1
NOX1 loss-of-function genetic variants in patients with inflammatory bowel disease.
Schwerd T, Bryant RV, Pandey S, Capitani M, Meran L, Cazier JB, Jung J, Mondal K, Parkes M, Mathew CG, Fiedler K, McCarthy DJ; WGS500 Consortium; Oxford IBD cohort study investigators; COLORS in IBD group investigators; UK IBD Genetics Consortium, Sullivan PB, Rodrigues A, Travis SPL, Moore C, Sambrook J, Ouwehand WH, Roberts DJ, Danesh J; INTERVAL Study, Russell RK, Wilson DC, Kelsen JR, Cornall R, Denson LA, Kugathasan S, Knaus UG, Serra EG, Anderson CA, Duerr RH, McGovern DP, Cho J, Powrie F, Li VS, Muise AM, Uhlig HH. Schwerd T, et al. Mucosal Immunol. 2018 Mar;11(2):562-574. doi: 10.1038/mi.2017.74. Epub 2017 Nov 1. Mucosal Immunol. 2018. PMID: 29091079 Free PMC article.
Clinical presentations of Wilson disease among Polish children.
Naorniakowska M, Dądalski M, Kamińska D, Jańczyk W, Lebensztejn D, Fyderek K, Wysocki J, Socha P. Naorniakowska M, et al. Among authors: fyderek k. Dev Period Med. 2016;20(3):216-221. Dev Period Med. 2016. PMID: 27941192
40 results