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

Year Number of Results
1950 1
1959 1
1965 1
1967 1
1970 2
1971 1
1972 2
1973 1
1974 2
1975 1
1976 3
1977 2
1978 1
1979 2
1980 3
1981 2
1982 5
1983 4
1984 6
1985 20
1986 23
1987 38
1988 68
1989 67
1990 75
1991 96
1992 101
1993 123
1994 143
1995 146
1996 176
1997 156
1998 145
1999 116
2000 155
2001 121
2002 141
2003 134
2004 177
2005 155
2006 158
2007 227
2008 218
2009 360
2010 240
2011 402
2012 391
2013 347
2014 364
2015 401
2016 445
2017 463
2018 405
2019 541
2020 542
2021 546
2022 556
2023 580
2024 173

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8,968 results

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Quoted phrase not found in phrase index: "Immunodeficiency 23"
Page 1
Monogenic early-onset lymphoproliferation and autoimmunity: Natural history of STAT3 gain-of-function syndrome.
Leiding JW, Vogel TP, Santarlas VGJ, Mhaskar R, Smith MR, Carisey A, Vargas-Hernández A, Silva-Carmona M, Heeg M, Rensing-Ehl A, Neven B, Hadjadj J, Hambleton S, Ronan Leahy T, Meesilpavikai K, Cunningham-Rundles C, Dutmer CM, Sharapova SO, Taskinen M, Chua I, Hague R, Klemann C, Kostyuchenko L, Morio T, Thatayatikom A, Ozen A, Scherbina A, Bauer CS, Flanagan SE, Gambineri E, Giovannini-Chami L, Heimall J, Sullivan KE, Allenspach E, Romberg N, Deane SG, Prince BT, Rose MJ, Bohnsack J, Mousallem T, Jesudas R, Santos Vilela MMD, O'Sullivan M, Pachlopnik Schmid J, Průhová Š, Klocperk A, Rees M, Su H, Bahna S, Baris S, Bartnikas LM, Chang Berger A, Briggs TA, Brothers S, Bundy V, Chan AY, Chandrakasan S, Christiansen M, Cole T, Cook MC, Desai MM, Fischer U, Fulcher DA, Gallo S, Gauthier A, Gennery AR, Gonçalo Marques J, Gottrand F, Grimbacher B, Grunebaum E, Haapaniemi E, Hämäläinen S, Heiskanen K, Heiskanen-Kosma T, Hoffman HM, Gonzalez-Granado LI, Guerrerio AL, Kainulainen L, Kumar A, Lawrence MG, Levin C, Martelius T, Neth O, Olbrich P, Palma A, Patel NC, Pozos T, Preece K, Lugo Reyes SO, Russell MA, Schejter Y, Seroogy C, Sinclair J, Skevofilax E, Suan D, Suez D, Szabolcs P, Velas… See abstract for full author list ➔ Leiding JW, et al. J Allergy Clin Immunol. 2023 Apr;151(4):1081-1095. doi: 10.1016/j.jaci.2022.09.002. Epub 2022 Oct 11. J Allergy Clin Immunol. 2023. PMID: 36228738 Free PMC article.
Infections were reported in 72% of the cohort. A cellular and humoral immunodeficiency was observed in 37% and 51% of patients, respectively. Clinical symptoms dramatically improved in patients treated with JAK inhibitors, while a variety of other immunomodulatory treatmen …
Infections were reported in 72% of the cohort. A cellular and humoral immunodeficiency was observed in 37% and 51% of patients, respe …
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 …
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 …
Diagnosis and management of Specific Antibody Deficiency.
Perez EE, Ballow M. Perez EE, et al. Immunol Allergy Clin North Am. 2020 Aug;40(3):499-510. doi: 10.1016/j.iac.2020.03.005. Epub 2020 Jun 9. Immunol Allergy Clin North Am. 2020. PMID: 32654695 Review.
Specific antibody deficiency is a primary immunodeficiency disease recognized by the International Union of Immunology Societies and defined by recurrent respiratory infections with normal immunoglobulins, but diminished antibody responses to polysaccharide antigens …
Specific antibody deficiency is a primary immunodeficiency disease recognized by the International Union of Immunology Societi …
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 …
Transfusion-associated graft-versus-host disease.
Rühl H, Bein G, Sachs UJ. Rühl H, et al. Transfus Med Rev. 2009 Jan;23(1):62-71. doi: 10.1016/j.tmrv.2008.09.006. Transfus Med Rev. 2009. PMID: 19056035 Review.
It is caused by the transfusion of viable T cells present in blood products that are not rejected by the transfusion recipient, either because of recipient immunodeficiency or because of a common HLA haplotype between the blood donor and recipient. ...Among the potential r …
It is caused by the transfusion of viable T cells present in blood products that are not rejected by the transfusion recipient, either becau …
Surgical implications of HIV infection.
Millar AJW, Cox SG. Millar AJW, et al. Pediatr Surg Int. 2022 Dec 8;39(1):39. doi: 10.1007/s00383-022-05333-6. Pediatr Surg Int. 2022. PMID: 36482099 Review.
According to the joint United Nations Programme on HIV/AIDS (UNAIDS), 37.7 million adults and children worldwide were estimated to be living with HIV or acquired immune deficiency syndrome (AIDS) at the end of 2020 [UNAIDS. (2022). http://www.unaids.org . ...
According to the joint United Nations Programme on HIV/AIDS (UNAIDS), 37.7 million adults and children worldwide were estimated to be living …
8,968 results