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

Year Number of Results
2004 1
2005 5
2006 7
2007 2
2008 3
2009 4
2010 2
2011 2
2012 1
2013 2
2014 1
2015 3
2016 1
2017 1
2018 1
2019 4
2020 4
2021 3
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45 results
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Page 1
Prevalence and pathogenicity of autoantibodies in patients with idiopathic CD4 lymphopenia.
Perez-Diez A, Wong CS, Liu X, Mystakelis H, Song J, Lu Y, Sheikh V, Bourgeois JS, Lisco A, Laidlaw E, Cudrici C, Zhu C, Li QZ, Freeman AF, Williamson PR, Anderson M, Roby G, Tsang JS, Siegel R, Sereti I. Perez-Diez A, et al. Among authors: cudrici c. J Clin Invest. 2020 Oct 1;130(10):5326-5337. doi: 10.1172/JCI136254. J Clin Invest. 2020. PMID: 32634122 Free PMC article.
Role of SIRT1 in autoimmune demyelination and neurodegeneration.
Martin A, Tegla CA, Cudrici CD, Kruszewski AM, Azimzadeh P, Boodhoo D, Mekala AP, Rus V, Rus H. Martin A, et al. Among authors: cudrici cd. Immunol Res. 2015 Mar;61(3):187-97. doi: 10.1007/s12026-014-8557-5. Immunol Res. 2015. PMID: 25281273 Review.
Generation of human induced pluripotent stem cells (NIHTVBi004-A, NIHTVBi005-A, NIHTVBi006-A, NIHTVBi007-A, NIHTVBi008-A) from 5 CADASIL patients with NOTCH3 mutation.
Chen G, Li Z, Liu Y, Chen D, Beers J, Cudrici C, Ferrante EA, Schwartzbeck R, Dmitrieva N, Yang D, Zou J, Iruela-Arispe ML, Boehm M. Chen G, et al. Among authors: cudrici c. Stem Cell Res. 2020 May;45:101821. doi: 10.1016/j.scr.2020.101821. Epub 2020 Apr 22. Stem Cell Res. 2020. PMID: 32344328 Free PMC article.
Generation of human induced pluripotent stem cell lines (NIHTVBi011-A, NIHTVBi012-A, NIHTVBi013-A) from autosomal dominant Hyper IgE syndrome (AD-HIES) patients carrying STAT3 mutation.
Jin H, Yu Z, Navarengom K, Liu Y, Dmitrieva N, Hsu AP, Schwartzbeck R, Cudrici C, Ferrante EA, Yang D, Holland SM, Freeman AF, Boehm M, Chen G. Jin H, et al. Among authors: cudrici c. Stem Cell Res. 2019 Dec;41:101586. doi: 10.1016/j.scr.2019.101586. Epub 2019 Oct 17. Stem Cell Res. 2019. PMID: 31707214 Free PMC article.
Morphology and chemical identity of periarticular and vascular calcification in a patient with the rare genetic disease of arterial calcification due to deficiency of CD73 (ACDC).
Lakshmipathy DR, Cudrici CD, Dyda F, Xu W, Ferrante EA, Nguyen DT, Carney KM, Rollison S, Chen MY, Nesti LJ, Boehm M, Brofferio A, Wen H. Lakshmipathy DR, et al. Among authors: cudrici cd. Radiol Case Rep. 2020 Aug 14;15(10):1883-1886. doi: 10.1016/j.radcr.2020.07.056. eCollection 2020 Oct. Radiol Case Rep. 2020. PMID: 32874378 Free PMC article.
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