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

Year Number of Results
1958 1
1959 1
1960 1
1961 3
1962 2
1965 7
1966 13
1967 21
1968 27
1969 33
1970 55
1971 70
1972 78
1973 62
1974 67
1975 106
1976 83
1977 81
1978 85
1979 84
1980 83
1981 103
1982 110
1983 120
1984 134
1985 187
1986 202
1987 195
1988 205
1989 231
1990 243
1991 267
1992 244
1993 346
1994 312
1995 355
1996 421
1997 425
1998 391
1999 473
2000 568
2001 470
2002 411
2003 443
2004 490
2005 461
2006 563
2007 541
2008 618
2009 638
2010 715
2011 846
2012 886
2013 818
2014 813
2015 768
2016 729
2017 683
2018 715
2019 344
2020 7
Text availability
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Article type
Publication date

Search Results

17,280 results
Results by year
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Page 1
The 2017 IUIS Phenotypic Classification for Primary Immunodeficiencies.
Bousfiha A, Jeddane L, Picard C, Ailal F, Bobby Gaspar H, Al-Herz W, Chatila T, Crow YJ, Cunningham-Rundles C, Etzioni A, Franco JL, Holland SM, Klein C, Morio T, Ochs HD, Oksenhendler E, Puck J, Tang MLK, Tangye SG, Torgerson TR, Casanova JL, Sullivan KE. Bousfiha A, et al. J Clin Immunol. 2018 Jan;38(1):129-143. doi: 10.1007/s10875-017-0465-8. Epub 2017 Dec 11. J Clin Immunol. 2018. PMID: 29226301 Free PMC article.
Adenosine deaminase deficiency: a review.
Flinn AM, Gennery AR. Flinn AM, et al. Orphanet J Rare Dis. 2018 Apr 24;13(1):65. doi: 10.1186/s13023-018-0807-5. Orphanet J Rare Dis. 2018. PMID: 29690908 Free PMC article. Review.
Foreword.
Aminoff MJ, Boller F, Swaab DF. Aminoff MJ, et al. Handb Clin Neurol. 2018;151:vii. doi: 10.1016/B978-0-444-63622-5.09992-7. Handb Clin Neurol. 2018. PMID: 29519483 No abstract available.
Exome and genome sequencing for inborn errors of immunity.
Meyts I, Bosch B, Bolze A, Boisson B, Itan Y, Belkadi A, Pedergnana V, Moens L, Picard C, Cobat A, Bossuyt X, Abel L, Casanova JL. Meyts I, et al. J Allergy Clin Immunol. 2016 Oct;138(4):957-969. doi: 10.1016/j.jaci.2016.08.003. J Allergy Clin Immunol. 2016. PMID: 27720020 Free PMC article. Review.
Primary immunodeficiency diseases: Genomic approaches delineate heterogeneous Mendelian disorders.
Stray-Pedersen A, Sorte HS, Samarakoon P, Gambin T, Chinn IK, Coban Akdemir ZH, Erichsen HC, Forbes LR, Gu S, Yuan B, Jhangiani SN, Muzny DM, Rødningen OK, Sheng Y, Nicholas SK, Noroski LM, Seeborg FO, Davis CM, Canter DL, Mace EM, Vece TJ, Allen CE, Abhyankar HA, Boone PM, Beck CR, Wiszniewski W, Fevang B, Aukrust P, Tjønnfjord GE, Gedde-Dahl T, Hjorth-Hansen H, Dybedal I, Nordøy I, Jørgensen SF, Abrahamsen TG, Øverland T, Bechensteen AG, Skogen V, Osnes LTN, Kulseth MA, Prescott TE, Rustad CF, Heimdal KR, Belmont JW, Rider NL, Chinen J, Cao TN, Smith EA, Caldirola MS, Bezrodnik L, Lugo Reyes SO, Espinosa Rosales FJ, Guerrero-Cursaru ND, Pedroza LA, Poli CM, Franco JL, Trujillo Vargas CM, Aldave Becerra JC, Wright N, Issekutz TB, Issekutz AC, Abbott J, Caldwell JW, Bayer DK, Chan AY, Aiuti A, Cancrini C, Holmberg E, West C, Burstedt M, Karaca E, Yesil G, Artac H, Bayram Y, Atik MM, Eldomery MK, Ehlayel MS, Jolles S, Flatø B, Bertuch AA, Hanson IC, Zhang VW, Wong LJ, Hu J, Walkiewicz M, Yang Y, Eng CM, Boerwinkle E, Gibbs RA, Shearer WT, Lyle R, Orange JS, Lupski JR. Stray-Pedersen A, et al. J Allergy Clin Immunol. 2017 Jan;139(1):232-245. doi: 10.1016/j.jaci.2016.05.042. Epub 2016 Jul 16. J Allergy Clin Immunol. 2017. PMID: 27577878 Free PMC article.
Primary Immunodeficiency: The Israeli Connection.
Etzioni A. Etzioni A. Isr Med Assoc J. 2018 Nov;20(11):703-706. Isr Med Assoc J. 2018. PMID: 30430801 Free article. No abstract available.
Clinically relevant immunology for practitioner.
Lieberman JA. Lieberman JA. Ann Allergy Asthma Immunol. 2019 Nov;123(5):422-423. doi: 10.1016/j.anai.2019.08.461. Ann Allergy Asthma Immunol. 2019. PMID: 31676019 No abstract available.
DNA ligase IV syndrome; a review.
Altmann T, Gennery AR. Altmann T, et al. Orphanet J Rare Dis. 2016 Oct 7;11(1):137. doi: 10.1186/s13023-016-0520-1. Orphanet J Rare Dis. 2016. PMID: 27717373 Free PMC article. Review.
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