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Results by year

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

Year Number of Results
1993 1
2001 4
2002 2
2003 2
2004 3
2005 4
2006 7
2007 9
2008 10
2009 7
2010 4
2011 7
2012 6
2013 5
2014 6
2015 6
2016 5
2017 5
2018 10
2019 9
2020 10
2021 20
2022 22
2023 8
2024 1

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Similar articles for PMID: 25326164

148 results

Results by year

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Page 1
A potential screening tool for IPEX syndrome.
Heltzer ML, Choi JK, Ochs HD, Sullivan KE, Torgerson TR, Ernst LM. Heltzer ML, et al. Pediatr Dev Pathol. 2007 Mar-Apr;10(2):98-105. doi: 10.2350/06-07-0130.1. Pediatr Dev Pathol. 2007. PMID: 17378693
Defective regulatory and effector T cell functions in patients with FOXP3 mutations.
Bacchetta R, Passerini L, Gambineri E, Dai M, Allan SE, Perroni L, Dagna-Bricarelli F, Sartirana C, Matthes-Martin S, Lawitschka A, Azzari C, Ziegler SF, Levings MK, Roncarolo MG. Bacchetta R, et al. J Clin Invest. 2006 Jun;116(6):1713-22. doi: 10.1172/JCI25112. J Clin Invest. 2006. PMID: 16741580 Free PMC article.
IPEX as a result of mutations in FOXP3.
van der Vliet HJ, Nieuwenhuis EE. van der Vliet HJ, et al. Clin Dev Immunol. 2007;2007:89017. doi: 10.1155/2007/89017. Clin Dev Immunol. 2007. PMID: 18317533 Free PMC article. Review.
148 results