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

Year Number of Results
2002 1
2004 4
2005 1
2006 1
2007 2
2008 2
2009 4
2010 5
2011 9
2012 7
2013 6
2014 11
2015 14
2016 9
2017 12
2018 13
2019 7
2020 8
2021 6
2022 7
2023 6
2024 5

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118 results

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Page 1
Characterising the spectrum of autosomal recessive hereditary hearing loss in Iran.
Sloan-Heggen CM, Babanejad M, Beheshtian M, Simpson AC, Booth KT, Ardalani F, Frees KL, Mohseni M, Mozafari R, Mehrjoo Z, Jamali L, Vaziri S, Akhtarkhavari T, Bazazzadegan N, Nikzat N, Arzhangi S, Sabbagh F, Otukesh H, Seifati SM, Khodaei H, Taghdiri M, Meyer NC, Daneshi A, Farhadi M, Kahrizi K, Smith RJ, Azaiez H, Najmabadi H. Sloan-Heggen CM, et al. Among authors: meyer nc. J Med Genet. 2015 Dec;52(12):823-9. doi: 10.1136/jmedgenet-2015-103389. Epub 2015 Oct 7. J Med Genet. 2015. PMID: 26445815 Free PMC article.
A multicenter, randomized, placebo-controlled, double-blind phase 3 trial with open-arm comparison indicates safety and efficacy of nephroprotective therapy with ramipril in children with Alport's syndrome.
Gross O, Tönshoff B, Weber LT, Pape L, Latta K, Fehrenbach H, Lange-Sperandio B, Zappel H, Hoyer P, Staude H, König S, John U, Gellermann J, Hoppe B, Galiano M, Hoecker B, Ehren R, Lerch C, Kashtan CE, Harden M, Boeckhaus J, Friede T; German Pediatric Nephrology (GPN) Study Group and EARLY PRO-TECT Alport Investigators. Gross O, et al. Kidney Int. 2020 Jun;97(6):1275-1286. doi: 10.1016/j.kint.2019.12.015. Epub 2020 Jan 17. Kidney Int. 2020. PMID: 32299679 Free article. Clinical Trial.
Mast cells-Good guys with a bad image?
Meyer N, Zenclussen AC. Meyer N, et al. Am J Reprod Immunol. 2018 Oct;80(4):e13002. doi: 10.1111/aji.13002. Epub 2018 Jun 19. Am J Reprod Immunol. 2018. PMID: 29917288 Review.
Mast cells as protectors of health.
Dudeck A, Köberle M, Goldmann O, Meyer N, Dudeck J, Lemmens S, Rohde M, Roldán NG, Dietze-Schwonberg K, Orinska Z, Medina E, Hendrix S, Metz M, Zenclussen AC, von Stebut E, Biedermann T. Dudeck A, et al. Among authors: meyer n. J Allergy Clin Immunol. 2019 Oct;144(4S):S4-S18. doi: 10.1016/j.jaci.2018.10.054. Epub 2018 Nov 20. J Allergy Clin Immunol. 2019. PMID: 30468774 Free article. Review.
Factor H Autoantibodies and Complement-Mediated Diseases.
Zhang Y, Ghiringhelli Borsa N, Shao D, Dopler A, Jones MB, Meyer NC, Pitcher GR, Taylor AO, Nester CM, Schmidt CQ, Smith RJH. Zhang Y, et al. Among authors: meyer nc. Front Immunol. 2020 Dec 15;11:607211. doi: 10.3389/fimmu.2020.607211. eCollection 2020. Front Immunol. 2020. PMID: 33384694 Free PMC article.
Complement Factor I Variants in Complement-Mediated Renal Diseases.
Zhang Y, Goodfellow RX, Ghiringhelli Borsa N, Dunlop HC, Presti SA, Meyer NC, Shao D, Roberts SM, Jones MB, Pitcher GR, Taylor AO, Nester CM, Smith RJH. Zhang Y, et al. Among authors: meyer nc. Front Immunol. 2022 May 10;13:866330. doi: 10.3389/fimmu.2022.866330. eCollection 2022. Front Immunol. 2022. PMID: 35619721 Free PMC article.
Genetic male infertility and mutation of CATSPER ion channels.
Hildebrand MS, Avenarius MR, Fellous M, Zhang Y, Meyer NC, Auer J, Serres C, Kahrizi K, Najmabadi H, Beckmann JS, Smith RJ. Hildebrand MS, et al. Among authors: meyer nc. Eur J Hum Genet. 2010 Nov;18(11):1178-84. doi: 10.1038/ejhg.2010.108. Epub 2010 Jul 21. Eur J Hum Genet. 2010. PMID: 20648059 Free PMC article. Review.
118 results