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

Year Number of Results
1966 1
1968 1
1972 1
1973 1
1974 1
1975 1
1976 4
1977 5
1978 2
1979 4
1980 2
1981 4
1982 3
1983 8
1984 9
1985 10
1986 18
1987 30
1988 41
1989 80
1990 75
1991 87
1992 92
1993 98
1994 133
1995 155
1996 138
1997 154
1998 188
1999 197
2000 190
2001 183
2002 211
2003 171
2004 298
2005 234
2006 274
2007 312
2008 305
2009 327
2010 352
2011 450
2012 524
2013 535
2014 557
2015 543
2016 539
2017 632
2018 650
2019 639
2020 677
2021 785
2022 686
2023 712
2024 247

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11,545 results

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Quoted phrase not found in phrase index: "Immunodeficiency 18"
Page 1
Reappraisal of Idiopathic CD4 Lymphocytopenia at 30 Years.
Lisco A, Ortega-Villa AM, Mystakelis H, Anderson MV, Mateja A, Laidlaw E, Manion M, Roby G, Higgins J, Kuriakose S, Walkiewicz MA, Similuk M, Leiding JW, Freeman AF, Sheikh V, Sereti I. Lisco A, et al. N Engl J Med. 2023 May 4;388(18):1680-1691. doi: 10.1056/NEJMoa2202348. N Engl J Med. 2023. PMID: 37133586 Free PMC article.
METHODS: We evaluated the clinical, genetic, immunologic, and prognostic characteristics of 108 patients who were enrolled during an 11-year period. ...We also performed longitudinal linear mixed-model analyses of T-cell count trajectories and evaluated predictors o …
METHODS: We evaluated the clinical, genetic, immunologic, and prognostic characteristics of 108 patients who were enrolled during an …
Efficacy and Safety of Subcutaneous Belimumab in Systemic Lupus Erythematosus: A Fifty-Two-Week Randomized, Double-Blind, Placebo-Controlled Study.
Stohl W, Schwarting A, Okada M, Scheinberg M, Doria A, Hammer AE, Kleoudis C, Groark J, Bass D, Fox NL, Roth D, Gordon D. Stohl W, et al. Arthritis Rheumatol. 2017 May;69(5):1016-1027. doi: 10.1002/art.40049. Epub 2017 Apr 7. Arthritis Rheumatol. 2017. PMID: 28118533 Free PMC article. Clinical Trial.
A total of 159 patients withdrew before the end of the study. At entry, mean SELENA-SLEDAI scores were 10.5 in the belimumab group and 10.3 in the placebo group. ...In the belimumab group, both time to and risk of severe flare were improved (median 171.0 days versus 118.0 …
A total of 159 patients withdrew before the end of the study. At entry, mean SELENA-SLEDAI scores were 10.5 in the belimumab group an …
Immunoglobulin replacement in hematological malignancies: a focus on evidence, alternatives, dosing strategy, and cessation rule.
Sim B, Ng JY, Teh BW, Talaulikar D. Sim B, et al. Leuk Lymphoma. 2023 Jan;64(1):18-29. doi: 10.1080/10428194.2022.2131424. Epub 2022 Oct 11. Leuk Lymphoma. 2023. PMID: 36218218
Acquired hypogammaglobulinemia or secondary immunodeficiency (SID) occurs commonly in hematological malignancies with increasing incidence and complexity in the era of modern therapies. ...Dosing and indications for cessation of IgRT are also inadequately characterized. Fu …
Acquired hypogammaglobulinemia or secondary immunodeficiency (SID) occurs commonly in hematological malignancies with increasing inci …
Treatment of hairy-cell leukemia.
Lill MC, Golde DW. Lill MC, et al. Blood Rev. 1990 Dec;4(4):238-44. doi: 10.1016/0268-960x(90)90003-b. Blood Rev. 1990. PMID: 1706207 Review.
The first line drug treatment remains interferon alpha given for 12-18 months, following which the patient is observed for clinical relapse. ...
The first line drug treatment remains interferon alpha given for 12-18 months, following which the patient is observed for cli …
Spectrum of Genetic Autoinflammatory Diseases Presenting with Cutaneous Symptoms.
Bonnekoh H, Butze M, Kallinich T, Kambe N, Kokolakis G, Krause K. Bonnekoh H, et al. Acta Derm Venereol. 2020 Mar 25;100(7):adv00091. doi: 10.2340/00015555-3427. Acta Derm Venereol. 2020. PMID: 32147748 Free PMC article. Review.
Many autoinflammatory diseases are caused by monogenic defects, which lead to disturbed immune signalling with release of proinflammatory mediators. In addition to interleukin-1beta and interleukin-18, interferons play a key role in the pathophysiology of these disorders. …
Many autoinflammatory diseases are caused by monogenic defects, which lead to disturbed immune signalling with release of proinflammatory me …
ADA Deficiency: Evaluation of the Clinical and Laboratory Features and the Outcome.
Cagdas D, Gur Cetinkaya P, Karaatmaca B, Esenboga S, Tan C, Yılmaz T, Gümüş E, Barış S, Kuşkonmaz B, Ozgur TT, Bali P, Santisteban I, Orhan D, Yüce A, Cetinkaya D, Boztug K, Hershfield M, Sanal O, Tezcan İ. Cagdas D, et al. J Clin Immunol. 2018 May;38(4):484-493. doi: 10.1007/s10875-018-0496-9. Epub 2018 May 9. J Clin Immunol. 2018. PMID: 29744787
RESULTS: Ten out of 13 patients were diagnosed as SCID, while 3 out of 13 were diagnosed as delayed-/late-onset ADA deficiency. Late-onset ADA deficiency patients had clinical and laboratory findings of combined immunodeficiency (CID). ...Enzyme replacement t …
RESULTS: Ten out of 13 patients were diagnosed as SCID, while 3 out of 13 were diagnosed as delayed-/late-onset ADA deficiency. Late- …
Autoimmune disorders associated with common variable immunodeficiency: prediction, diagnosis, and treatment.
Yazdanpanah N, Rezaei N. Yazdanpanah N, et al. Expert Rev Clin Immunol. 2022 Dec;18(12):1265-1283. doi: 10.1080/1744666X.2022.2132938. Epub 2022 Oct 17. Expert Rev Clin Immunol. 2022. PMID: 36197300
INTRODUCTION: Common variable immunodeficiency (CVID) is the most common symptomatic primary immunodeficiency. ...
INTRODUCTION: Common variable immunodeficiency (CVID) is the most common symptomatic primary immunodeficiency. ...
Clinical and Immunological Features of 96 Moroccan Children with SCID Phenotype: Two Decades' Experience.
Benhsaien I, Ailal F, El Bakkouri J, Jeddane L, Ouair H, Admou B, Bouskraoui M, Hbibi M, Hida M, Amenzoui N, Jouhadi Z, El Hafidi N, Rada N, Benajiba N, Abilkassem R, Badou A, Bousfiha AA. Benhsaien I, et al. J Clin Immunol. 2021 Apr;41(3):631-638. doi: 10.1007/s10875-020-00960-x. Epub 2021 Jan 7. J Clin Immunol. 2021. PMID: 33411152
Severe combined immunodeficiency (SCID) is a heterogeneous group of primary immunodeficiency diseases (PIDs) characterized by a lack of autologous T lymphocytes. ...The distribution of SCID phenotypes was as follows: T-B-NK+ in 44.5%, T-B-NK- in 32%, T-B+NK- in 1 …
Severe combined immunodeficiency (SCID) is a heterogeneous group of primary immunodeficiency diseases (PIDs) characterized by …
Evaluation of primary immunodeficiency disease in children.
Reust CE. Reust CE. Am Fam Physician. 2013 Jun 1;87(11):773-8. Am Fam Physician. 2013. PMID: 23939499 Free article. Review.
One in 2,000 children younger than 18 years is thought to have a primary immunodeficiency disease. ...Children with these diseases tend to have bacterial or fungal infections with unusual organisms, or unusually severe and recurrent infections with common organisms. …
One in 2,000 children younger than 18 years is thought to have a primary immunodeficiency disease. ...Children with these dise …
Learning and memory function in young people with and without perinatal HIV in England.
Arenas-Pinto A, Judd A, Melvin D, Le Prevost M, Foster C, Sturgeon K, Winston A, Thompson LC, Gibb DM, Castro H; Adolescents and Adults Living with Perinatal HIV (AALPHI) Steering Committee. Arenas-Pinto A, et al. PLoS One. 2022 Sep 15;17(9):e0273645. doi: 10.1371/journal.pone.0273645. eCollection 2022. PLoS One. 2022. PMID: 36107958 Free PMC article.
The effect of predictors on test scores in the three domains with the lowest z-scores were analysed using linear regression. 139(59%) and 48(71%) PHIV and HIV-negative YP were female, 202(86%) and 52(76%) Black, and median age was 19 [17, 21] and 18 [1 …
The effect of predictors on test scores in the three domains with the lowest z-scores were analysed using linear regres …
11,545 results
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