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

Year Number of Results
1975 1
1976 1
1977 4
1978 4
1979 1
1980 3
1981 4
1982 8
1983 11
1984 1
1985 10
1986 7
1987 7
1988 3
1989 4
1990 2
1991 1
1992 5
1993 7
1994 5
1995 3
1996 1
1997 7
1998 5
1999 3
2000 4
2001 8
2002 1
2003 9
2004 4
2005 7
2006 10
2007 5
2008 4
2009 6
2010 6
2011 7
2012 12
2013 10
2014 8
2015 7
2016 5
2017 4
2018 1
2019 5
2020 6
2021 8
2022 1
2023 3
2024 3
2025 0

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241 results

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Page 1
The European Society for Immunodeficiencies (ESID) Registry Working Definitions for the Clinical Diagnosis of Inborn Errors of Immunity.
Seidel MG, Kindle G, Gathmann B, Quinti I, Buckland M, van Montfrans J, Scheible R, Rusch S, Gasteiger LM, Grimbacher B, Mahlaoui N, Ehl S; ESID Registry Working Party and collaborators. Seidel MG, et al. J Allergy Clin Immunol Pract. 2019 Jul-Aug;7(6):1763-1770. doi: 10.1016/j.jaip.2019.02.004. Epub 2019 Feb 15. J Allergy Clin Immunol Pract. 2019. PMID: 30776527
A neomorphic mutation in the interferon activation domain of IRF4 causes a dominant primary immunodeficiency.
Thouenon R, Chentout L, Moreno-Corona N, Poggi L, Lombardi EP, Hoareau B, Schmitt Y, Lagresle-Peyrou C, Bustamante J, André I, Cavazzana M, Durandy A, Casanova JL, Galicier L, Fadlallah J, Fischer A, Kracker S. Thouenon R, et al. Among authors: durandy a. J Exp Med. 2023 Jun 5;220(6):e20221292. doi: 10.1084/jem.20221292. Epub 2023 Mar 14. J Exp Med. 2023. PMID: 36917008 Free PMC article.
Activated PI3Kinase Delta Syndrome-A Multifaceted Disease.
Thouenon R, Moreno-Corona N, Poggi L, Durandy A, Kracker S. Thouenon R, et al. Among authors: durandy a. Front Pediatr. 2021 Jun 25;9:652405. doi: 10.3389/fped.2021.652405. eCollection 2021. Front Pediatr. 2021. PMID: 34249806 Free PMC article. Review.
Primary antibody deficiencies.
Durandy A, Kracker S, Fischer A. Durandy A, et al. Nat Rev Immunol. 2013 Jul;13(7):519-33. doi: 10.1038/nri3466. Epub 2013 Jun 14. Nat Rev Immunol. 2013. PMID: 23765059 Review.
Hyper-IgM syndromes.
Durandy A, Peron S, Fischer A. Durandy A, et al. Curr Opin Rheumatol. 2006 Jul;18(4):369-76. doi: 10.1097/01.bor.0000231905.12172.b5. Curr Opin Rheumatol. 2006. PMID: 16763457 Review.
Morbidity-free survival in extremely premature infants after changes of clinical practices according to evidence-based guidelines: a quality improvement uncontrolled before-after study in a neonatal intensive care unit.
Bissainte-Zelbin V, Durandy A, Lecoq L, Wachter PY, Bennour O, Micklethwait F, Boileau P, Motte-Signoret E. Bissainte-Zelbin V, et al. Among authors: durandy a. Eur J Pediatr. 2024 Nov 14;184(1):11. doi: 10.1007/s00431-024-05842-7. Eur J Pediatr. 2024. PMID: 39542904
A homozygous PMS2 founder mutation with an attenuated constitutional mismatch repair deficiency phenotype.
Li L, Hamel N, Baker K, McGuffin MJ, Couillard M, Gologan A, Marcus VA, Chodirker B, Chudley A, Stefanovici C, Durandy A, Hegele RA, Feng BJ, Goldgar DE, Zhu J, De Rosa M, Gruber SB, Wimmer K, Young B, Chong G, Tischkowitz MD, Foulkes WD. Li L, et al. Among authors: durandy a. J Med Genet. 2015 May;52(5):348-52. doi: 10.1136/jmedgenet-2014-102934. Epub 2015 Feb 17. J Med Genet. 2015. PMID: 25691505
241 results