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

Year Number of Results
1998 1
2000 5
2001 4
2002 1
2003 3
2004 2
2005 1
2006 2
2007 3
2008 2
2009 1
2010 4
2011 3
2012 3
2013 1
2014 2
2015 4
2016 2
2017 2
2018 3
2019 7
2020 5
2021 4
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61 results
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Page 1
WHIM Syndrome: from Pathogenesis Towards Personalized Medicine and Cure.
Heusinkveld LE, Majumdar S, Gao JL, McDermott DH, Murphy PM. Heusinkveld LE, et al. Among authors: mcdermott dh. J Clin Immunol. 2019 Aug;39(6):532-556. doi: 10.1007/s10875-019-00665-w. Epub 2019 Jul 16. J Clin Immunol. 2019. PMID: 31313072 Free PMC article. Review.
Plerixafor for the Treatment of WHIM Syndrome.
McDermott DH, Pastrana DV, Calvo KR, Pittaluga S, Velez D, Cho E, Liu Q, Trout HH 3rd, Neves JF, Gardner PJ, Bianchi DA, Blair EA, Landon EM, Silva SL, Buck CB, Murphy PM. McDermott DH, et al. N Engl J Med. 2019 Jan 10;380(2):163-170. doi: 10.1056/NEJMoa1808575. N Engl J Med. 2019. PMID: 30625055 Free PMC article.
Absence of mucosal-associated invariant T cells in a person with a homozygous point mutation in MR1.
Howson LJ, Awad W, von Borstel A, Lim HJ, McWilliam HEG, Sandoval-Romero ML, Majumdar S, Hamzeh AR, Andrews TD, McDermott DH, Murphy PM, Le Nours J, Mak JYW, Liu L, Fairlie DP, McCluskey J, Villadangos JA, Cook MC, Turner SJ, Davey MS, Ojaimi S, Rossjohn J. Howson LJ, et al. Among authors: mcdermott dh. Sci Immunol. 2020 Jul 24;5(49):eabc9492. doi: 10.1126/sciimmunol.abc9492. Sci Immunol. 2020. PMID: 32709702
JAGN1 mutations in severe congenital neutropenia.
McDermott DH, Malech HL. McDermott DH, et al. Br J Haematol. 2021 Jan;192(1):9-10. doi: 10.1111/bjh.17135. Epub 2020 Nov 18. Br J Haematol. 2021. PMID: 33207009 No abstract available.
Chromoanasynthesis as a cause of Jacobsen syndrome.
Anzick S, Thurm A, Burkett S, Velez D, Cho E, Chlebowski C, Virtaneva K, Bruno D, Martin CB, Lang DM, Brooks B, Martens C, McDermott DH, Murphy PM. Anzick S, et al. Among authors: mcdermott dh. Am J Med Genet A. 2020 Nov;182(11):2533-2539. doi: 10.1002/ajmg.a.61824. Epub 2020 Aug 25. Am J Med Genet A. 2020. PMID: 32841469
Discovery of several thousand highly diverse circular DNA viruses.
Tisza MJ, Pastrana DV, Welch NL, Stewart B, Peretti A, Starrett GJ, Pang YS, Krishnamurthy SR, Pesavento PA, McDermott DH, Murphy PM, Whited JL, Miller B, Brenchley J, Rosshart SP, Rehermann B, Doorbar J, Ta'ala BA, Pletnikova O, Troncoso JC, Resnick SM, Bolduc B, Sullivan MB, Varsani A, Segall AM, Buck CB. Tisza MJ, et al. Among authors: mcdermott dh. Elife. 2020 Feb 4;9:e51971. doi: 10.7554/eLife.51971. Elife. 2020. PMID: 32014111 Free PMC article.
Abnormal Newborn Screen in a WHIM Syndrome Infant.
Evans MO 2nd, McDermott DH, Murphy PM, Petersen MM. Evans MO 2nd, et al. Among authors: mcdermott dh. J Clin Immunol. 2019 Nov;39(8):839-841. doi: 10.1007/s10875-019-00686-5. Epub 2019 Sep 6. J Clin Immunol. 2019. PMID: 31493092 Free PMC article. No abstract available.
Case Report: Ocular toxoplasmosis in a WHIM syndrome immunodeficiency patient.
McDermott DH, Heusinkveld LE, Zein WM, Sen HN, Marquesen MM, Parta M, Rosenzweig SD, Fahle GA, Keller MD, Wiley HE, Murphy PM. McDermott DH, et al. F1000Res. 2019 Jan 2;8:2. doi: 10.12688/f1000research.16825.2. eCollection 2019. F1000Res. 2019. PMID: 31249677 Free PMC article.
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