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Year Number of Results
1972 1
1975 2
1976 2
1979 1
1980 2
1981 3
1982 3
1983 5
1984 11
1985 12
1986 18
1987 28
1988 48
1989 50
1990 59
1991 66
1992 87
1993 115
1994 121
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1996 144
1997 128
1998 135
1999 121
2000 160
2001 133
2002 135
2003 147
2004 168
2005 197
2006 180
2007 273
2008 229
2009 391
2010 278
2011 395
2012 344
2013 359
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2015 407
2016 384
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2018 373
2019 464
2020 461
2021 495
2022 505
2023 540
2024 159

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8,430 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 t …
Infections were reported in 72% of the cohort. A cellular and humoral immunodeficiency was observed in 37% and 51% of patients …
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.
Anaphylactic reactions are a known complication in some IgA-deficient patients receiving blood or plasma transfusions. It is of particular interest that anaphylaxis has been observed in patients with common variable immunodeficiency (CVID) who are receiving intraven …
Anaphylactic reactions are a known complication in some IgA-deficient patients receiving blood or plasma transfusions. It is of particular i …
Clinical and functional spectrum of RAC2-related immunodeficiency.
Donkó Á, Sharapova SO, Kabat J, Ganesan S, Hauck FH, Bergerson JRE, Marois L, Abbott J, Moshous D, Williams KW, Campbell N, Martin PL, Lagresle-Peyrou C, Trojan T, Kuzmenko NB, Deordieva EA, Raykina EV, Abers MS, Abolhassani H, Barlogis V, Milla C, Hall G, Mousallem T, Church J, Kapoor N, Cros G, Chapdelaine H, Franco-Jarava C, Lopez-Lerma I, Miano M, Leiding JW, Klein C, Stasia MJ, Fischer A, Hsiao KC, Martelius T, Sepännen MRJ, Barmettler S, Walter J, Masmas TN, Mukhina AA, Falcone EL, Kracker S, Shcherbina A, Holland SM, Leto TL, Hsu AP. Donkó Á, et al. Blood. 2024 Apr 11;143(15):1476-1487. doi: 10.1182/blood.2023022098. Blood. 2024. PMID: 38194689
Mutations in the small Rho-family guanosine triphosphate hydrolase RAC2, critical for actin cytoskeleton remodeling and intracellular signal transduction, are associated with neonatal severe combined immunodeficiency (SCID), infantile neutrophilic disorder resembling leuko …
Mutations in the small Rho-family guanosine triphosphate hydrolase RAC2, critical for actin cytoskeleton remodeling and intracellular signal …
The Medication Experience of TB/HIV Coinfected Patients: Qualitative Study.
Resende NH, Martins UCM, Ramalho-de-Oliveira D, Silva DID, de Miranda SS, Reis AMM, Carvalho WDS, Mendonça SAM. Resende NH, et al. Int J Environ Res Public Health. 2022 Nov 17;19(22):15153. doi: 10.3390/ijerph192215153. Int J Environ Res Public Health. 2022. PMID: 36429870 Free PMC article.
Tuberculosis (TB) and human immunodeficiency virus/acquired immunodeficiency syndrome (HIV/AIDS) pharmacotherapy and the stigma related to both diseases are complex. ...Resolvability, associated with the patient's understanding of relief from signs and symptoms and …
Tuberculosis (TB) and human immunodeficiency virus/acquired immunodeficiency syndrome (HIV/AIDS) pharmacotherapy and the stigm …
Disease Progression of WHIM Syndrome in an International Cohort of 66 Pediatric and Adult Patients.
Geier CB, Ellison M, Cruz R, Pawar S, Leiss-Piller A, Zmajkovicova K, McNulty SM, Yilmaz M, Evans MO 2nd, Gordon S, Ujhazi B, Wiest I, Abolhassani H, Aghamohammadi A, Barmettler S, Bhar S, Bondarenko A, Bolyard AA, Buchbinder D, Cada M, Cavieres M, Connelly JA, Dale DC, Deordieva E, Dorsey MJ, Drysdale SB, Ehl S, Elfeky R, Fioredda F, Firkin F, Förster-Waldl E, Geng B, Goda V, Gonzalez-Granado L, Grunebaum E, Grzesk E, Henrickson SE, Hilfanova A, Hiwatari M, Imai C, Ip W, Jyonouchi S, Kanegane H, Kawahara Y, Khojah AM, Kim VH, Kojić M, Kołtan S, Krivan G, Langguth D, Lau YL, Leung D, Miano M, Mersyanova I, Mousallem T, Muskat M, Naoum FA, Noronha SA, Ouederni M, Ozono S, Richmond GW, Sakovich I, Salzer U, Schuetz C, Seeborg FO, Sharapova SO, Sockel K, Volokha A, von Bonin M, Warnatz K, Wegehaupt O, Weinberg GA, Wong KJ, Worth A, Yu H, Zharankova Y, Zhao X, Devlin L, Badarau A, Csomos K, Keszei M, Pereira J, Taveras AG, Beaussant-Cohen SL, Ong MS, Shcherbina A, Walter JE. Geier CB, et al. J Clin Immunol. 2022 Nov;42(8):1748-1765. doi: 10.1007/s10875-022-01312-7. Epub 2022 Aug 10. J Clin Immunol. 2022. PMID: 35947323 Free PMC article.
Warts, hypogammaglobulinemia, infections, and myelokathexis (WHIM) syndrome (WS) is a combined immunodeficiency caused by gain-of-function mutations in the C-X-C chemokine receptor type 4 (CXCR4) gene. ...Of 17 distinct CXCR4 genetic variants within our cohort, 11 were nov …
Warts, hypogammaglobulinemia, infections, and myelokathexis (WHIM) syndrome (WS) is a combined immunodeficiency caused by gain-of-fun …
Rituximab-induced hypogammaglobulinemia and infection risk in pediatric patients.
Labrosse R, Barmettler S, Derfalvi B, Blincoe A, Cros G, Lacombe-Barrios J, Barsalou J, Yang N, Alrumayyan N, Sinclair J, Ong MS, Camargo CA Jr, Walter J, Haddad E. Labrosse R, et al. J Allergy Clin Immunol. 2021 Aug;148(2):523-532.e8. doi: 10.1016/j.jaci.2021.03.041. Epub 2021 Apr 20. J Allergy Clin Immunol. 2021. PMID: 33862010
Nine patients (4.3%) within the study were subsequently diagnosed with a primary immunodeficiency, 7 of which received rituximab for autoimmune cytopenias. ...Low IgG levels are associated with a significant increase in serious infections, and underlying primary immunod …
Nine patients (4.3%) within the study were subsequently diagnosed with a primary immunodeficiency, 7 of which received rituximab for …
A summertime pause in immunoglobulin replacement therapy: a prospective real-world analysis.
Hémar V, Rivière E, Greib C, Machelart I, Roucoules M, Prot C, Pellegrin JL, Viallard JF, Lazaro E. Hémar V, et al. Immunotherapy. 2021 Dec;13(18):1491-1499. doi: 10.2217/imt-2020-0313. Epub 2021 Nov 8. Immunotherapy. 2021. PMID: 34743547 Clinical Trial.
Results: IgRT was interrupted in 23 patients from June to October. Patients who underwent an SP were older, more likely to have secondary immunodeficiency (SID) and received lower doses of immunoglobulin and more antibiotics during winter. ...We report here for the …
Results: IgRT was interrupted in 23 patients from June to October. Patients who underwent an SP were older, more likely to have secon …
Interleukin 17-producing T helper cells in alloimmunity.
Benghiat FS, Charbonnier LM, Vokaer B, De Wilde V, Le Moine A. Benghiat FS, et al. Transplant Rev (Orlando). 2009 Jan;23(1):11-8. doi: 10.1016/j.trre.2008.08.007. Transplant Rev (Orlando). 2009. PMID: 19027613 Review.
Herein, we discuss arguments in favor of a Th17-mediated alternative pathway of allograft rejection based on clinical and experimental observations drawn from the literature. We also discuss the complex interplays among regulatory T cells and Th17 cells in the allogeneic c …
Herein, we discuss arguments in favor of a Th17-mediated alternative pathway of allograft rejection based on clinical and experimental ob …
Primary Immunodeficiency Disorders Among North Indian Children.
Gupta D, Thakral D, Kumar P, Kabra SK, Lodha R, Kumari R, Mohanty SK, Chakraborty S, Bagri N, Mitra DK. Gupta D, et al. Indian J Pediatr. 2019 Oct;86(10):885-891. doi: 10.1007/s12098-019-02971-y. Epub 2019 Jun 8. Indian J Pediatr. 2019. PMID: 31177511
The diagnosis of index study subjects included combined humoral and cellular immunodeficiency (29%), phagocytic defects (29%), followed by predominantly antibody deficiency (18%), innate immunity and dysregulation (17%) and other well-defined syndromes (7%). …
The diagnosis of index study subjects included combined humoral and cellular immunodeficiency (29%), phagocytic defects (29%), follow …
8,430 results