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

Year Number of Results
1964 1
1967 1
1968 6
1970 1
1971 3
1972 4
1974 2
1975 1
1977 2
1978 3
1979 2
1982 1
1983 1
1984 3
1985 7
1986 9
1987 16
1988 30
1989 38
1990 58
1991 35
1992 26
1993 24
1994 62
1995 26
1996 52
1997 41
1998 40
1999 37
2000 44
2001 37
2002 54
2003 57
2004 52
2005 53
2006 46
2007 66
2008 40
2009 73
2010 74
2011 92
2012 82
2013 71
2014 66
2015 84
2016 81
2017 90
2018 58
2019 49
2020 46
2021 78
2022 110
2023 97
2024 23

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2,029 results

Results by year

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Page 1
Treatment of inflammatory complications in common variable immunodeficiency (CVID): current concepts and future perspectives.
Fevang B. Fevang B. Expert Rev Clin Immunol. 2023 Jun;19(6):627-638. doi: 10.1080/1744666X.2023.2198208. Epub 2023 Apr 6. Expert Rev Clin Immunol. 2023. PMID: 36996348 Review.
INTRODUCTION: Patients with common variable immunodeficiency (CVID) have a high frequency of inflammatory complications like autoimmune cytopenias, interstitial lung disease and enteropathy. ...Therapies of potential interest and wider use in CVID include mTOR-inhibitors l …
INTRODUCTION: Patients with common variable immunodeficiency (CVID) have a high frequency of inflammatory complications like autoimmu …
Anaphylaxis to IVIG.
Williams SJ, Gupta S. Williams SJ, et al. Arch Immunol Ther Exp (Warsz). 2017 Feb;65(1):11-19. doi: 10.1007/s00005-016-0410-1. Epub 2016 Jul 13. Arch Immunol Ther Exp (Warsz). 2017. PMID: 27412077 Free article. Review.
It is of particular interest that anaphylaxis has been observed in patients with common variable immunodeficiency (CVID) who are receiving intravenous gammaglobulin (IVIG), and in that, although these patients have an impaired response to common vaccines, they retain the a …
It is of particular interest that anaphylaxis has been observed in patients with common variable immunodeficiency (CVID) who are rece …
Hyper-IgE syndrome.
Minegishi Y. Minegishi Y. Curr Opin Immunol. 2009 Oct;21(5):487-92. doi: 10.1016/j.coi.2009.07.013. Epub 2009 Aug 28. Curr Opin Immunol. 2009. PMID: 19717292 Review.
Hyper-IgE syndrome (HIES) is a complex primary immunodeficiency characterized by atopic dermatitis associated with extremely high serum IgE levels and susceptibility to infections with extracellular bacteria. ...In both patients, signal transduction for multiple cytokines, …
Hyper-IgE syndrome (HIES) is a complex primary immunodeficiency characterized by atopic dermatitis associated with extremely high ser …
NeuroAIDS in children.
Wilmshurst JM, Hammond CK, Donald K, Hoare J, Cohen K, Eley B. Wilmshurst JM, et al. Handb Clin Neurol. 2018;152:99-116. doi: 10.1016/B978-0-444-63849-6.00008-6. Handb Clin Neurol. 2018. PMID: 29604987 Review.
The human immunodeficiency virus-1 (HIV-1) enters the central nervous system compartment within the first few weeks of systemic HIV infection and may cause a spectrum of neurologic complications. ...
The human immunodeficiency virus-1 (HIV-1) enters the central nervous system compartment within the first few weeks of systemic HIV i …
Genetic immunodeficiency diseases.
Abrams M, Paller A. Abrams M, et al. Adv Dermatol. 2007;23:197-229. doi: 10.1016/j.yadr.2007.08.001. Adv Dermatol. 2007. PMID: 18159903 Review.
The approach to the patient with genetic immunodeficiency is multidisciplinary, and requires close interaction between the primary care physician, immunologist, and other specialists. ...The underlying genetic basis is now known for most forms of immunodeficiency, w …
The approach to the patient with genetic immunodeficiency is multidisciplinary, and requires close interaction between the primary ca …
Recommendations for Management of Secondary Antibody Deficiency in Multiple Myeloma.
Giralt S, Jolles S, Kerre T, Lazarus HM, Mustafa SS, Papanicolaou GA, Ria R, Vinh DC, Wingard JR. Giralt S, et al. Clin Lymphoma Myeloma Leuk. 2023 Oct;23(10):719-732. doi: 10.1016/j.clml.2023.05.008. Epub 2023 May 23. Clin Lymphoma Myeloma Leuk. 2023. PMID: 37353432 Free article. Review.
Secondary antibody deficiency (SAD) is a subtype of secondary immunodeficiency characterized by low serum antibody concentrations (hypogammaglobulinemia) or poor antibody function. ...Firstly, all patients with MM should be suspected to have SAD regardless of serum …
Secondary antibody deficiency (SAD) is a subtype of secondary immunodeficiency characterized by low serum antibody concentrati …
Genetic immunodeficiency disorders.
Paller AS. Paller AS. Clin Dermatol. 2005 Jan-Feb;23(1):68-77. doi: 10.1016/j.clindermatol.2004.09.011. Clin Dermatol. 2005. PMID: 15708291 Review.
In this review, selected immunodeficiency disorders are presented in which the cutaneous signs are distinctive and contribute to the diagnosis of the condition. ...The underlying molecular basis for most genetic immunodeficiencies is now understood, allowing improve …
In this review, selected immunodeficiency disorders are presented in which the cutaneous signs are distinctive and contribute to the …
1,2,3-Triazole hybrids with anti-HIV-1 activity.
Feng LS, Zheng MJ, Zhao F, Liu D. Feng LS, et al. Arch Pharm (Weinheim). 2021 Jan;354(1):e2000163. doi: 10.1002/ardp.202000163. Epub 2020 Sep 22. Arch Pharm (Weinheim). 2021. PMID: 32960467 Review.
The human immunodeficiency virus type 1 (HIV-1) is the major etiological agent responsible for the acquired immunodeficiency syndrome (AIDS), which is a serious infectious disease and remains one of the most prevalent problems at present. ...
The human immunodeficiency virus type 1 (HIV-1) is the major etiological agent responsible for the acquired immunodeficiency s …
2,029 results