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

Year Number of Results
1983 1
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1991 2
1993 1
1994 3
1995 3
1996 5
1997 2
1998 5
1999 3
2000 3
2001 9
2002 6
2003 2
2004 3
2005 2
2006 5
2007 5
2008 12
2009 6
2010 9
2011 7
2012 12
2013 12
2014 5
2015 14
2016 10
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2023 8
2024 5

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201 results

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Page 1
Common Variable Immunodeficiency: Epidemiology, Pathogenesis, Clinical Manifestations, Diagnosis, Classification, and Management.
Yazdani R, Habibi S, Sharifi L, Azizi G, Abolhassani H, Olbrich P, Aghamohammadi A. Yazdani R, et al. J Investig Allergol Clin Immunol. 2020;30(1):14-34. doi: 10.18176/jiaci.0388. Epub 2019 Feb 11. J Investig Allergol Clin Immunol. 2020. PMID: 30741636 Free article. Review.
Common variable immunodeficiency (CVID) is a heterogeneous disorder characterized by hypogammaglobulinemia and increased susceptibility to recurrent bacterial infections. ...
Common variable immunodeficiency (CVID) is a heterogeneous disorder characterized by hypogammaglobulinemia and increase
22q11.2 deletion syndrome.
McDonald-McGinn DM, Sullivan KE, Marino B, Philip N, Swillen A, Vorstman JA, Zackai EH, Emanuel BS, Vermeesch JR, Morrow BE, Scambler PJ, Bassett AS. McDonald-McGinn DM, et al. Nat Rev Dis Primers. 2015 Nov 19;1:15071. doi: 10.1038/nrdp.2015.71. Nat Rev Dis Primers. 2015. PMID: 27189754 Free PMC article. Review.
22q11.2 deletion syndrome (22q11.2DS) is the most common chromosomal microdeletion disorder, estimated to result mainly from de novo non-homologous meiotic recombination events occurring in approximately 1 in every 1,000 fetuses. The first description in the …
22q11.2 deletion syndrome (22q11.2DS) is the most common chromosomal microdeletion disorder, estimated to result mainly from de novo …
Common Variable Immunodeficiency.
Remiker A, Bolling K, Verbsky J. Remiker A, et al. Med Clin North Am. 2024 Jan;108(1):107-121. doi: 10.1016/j.mcna.2023.06.012. Epub 2023 Jul 21. Med Clin North Am. 2024. PMID: 37951645 Review.
Common variable immunodeficiency (CVID) is the most common primary immune deficiency characterized by impaired production of specific immunoglobulin. ...
Common variable immunodeficiency (CVID) is the most common primary immune deficiency characterized by impaired p
Immune dysregulation.
Long A, Kleiner A, Looney RJ. Long A, et al. J Allergy Clin Immunol. 2023 Jan;151(1):70-80. doi: 10.1016/j.jaci.2022.11.001. J Allergy Clin Immunol. 2023. PMID: 36608984 Free article. Review.
There is increasing evidence that altered microbiome and gut barrier dysfunction contribute to systemic inflammation in patients with primary immunodeficiency and in patients with rheumatic disease. Recent research provides insight into the process of induction and maturat …
There is increasing evidence that altered microbiome and gut barrier dysfunction contribute to systemic inflammation in patients with primar …
International Consensus Document (ICON): Common Variable Immunodeficiency Disorders.
Bonilla FA, Barlan I, Chapel H, Costa-Carvalho BT, Cunningham-Rundles C, de la Morena MT, Espinosa-Rosales FJ, Hammarström L, Nonoyama S, Quinti I, Routes JM, Tang ML, Warnatz K. Bonilla FA, et al. J Allergy Clin Immunol Pract. 2016 Jan-Feb;4(1):38-59. doi: 10.1016/j.jaip.2015.07.025. Epub 2015 Nov 7. J Allergy Clin Immunol Pract. 2016. PMID: 26563668 Free PMC article.
The International Collaboration in Asthma, Allergy and Immunology initiated an international coalition among the American Academy of Allergy, Asthma & Immunology; the European Academy of Allergy and Clinical Immunology; the World Allergy Organization; and the American College …
The International Collaboration in Asthma, Allergy and Immunology initiated an international coalition among the American Academy of Allergy …
Agammaglobulinemia: from X-linked to Autosomal Forms of Disease.
Cardenas-Morales M, Hernandez-Trujillo VP. Cardenas-Morales M, et al. Clin Rev Allergy Immunol. 2022 Aug;63(1):22-35. doi: 10.1007/s12016-021-08870-5. Epub 2021 Jul 9. Clin Rev Allergy Immunol. 2022. PMID: 34241796 Free PMC article. Review.
Interruptions or alterations in the B cell development pathway can lead to primary B cell immunodeficiency with resultant absence or diminished immunoglobulin production. While the most common cause of congenital agammaglobulinemia is X-linked agammaglobulinemia (XL …
Interruptions or alterations in the B cell development pathway can lead to primary B cell immunodeficiency with resultant absence or …
Lymphocytic Esophagitis: Current Understanding and Controversy.
Pittman ME. Pittman ME. Am J Surg Pathol. 2022 Jan 1;46(1):e55-e63. doi: 10.1097/PAS.0000000000001667. Am J Surg Pathol. 2022. PMID: 33481383 Review.
Clinically, the majority of patients who present with histologically confirmed LE are older women or patients with underlying immunologic abnormalities, such as Crohn disease, rheumatologic disorders, or common variable immunodeficiency. The most common
Clinically, the majority of patients who present with histologically confirmed LE are older women or patients with underlying immunologic ab …
Systematic review of case reports of antiphospholipid syndrome following infection.
Abdel-Wahab N, Lopez-Olivo MA, Pinto-Patarroyo GP, Suarez-Almazor ME. Abdel-Wahab N, et al. Lupus. 2016 Dec;25(14):1520-1531. doi: 10.1177/0961203316640912. Epub 2016 Apr 7. Lupus. 2016. PMID: 27060064 Free PMC article. Review.
The most common preceding infection was viral (55.6%). In cases that developed thromboembolic events Human immunodeficiency and Hepatitis C viruses were the most frequently reported. ...Few patients in groups 1 and 2 had persistent antiphospholipid antibodies …
The most common preceding infection was viral (55.6%). In cases that developed thromboembolic events Human immunodeficiency an …
AGA Clinical Practice Update on Management of Refractory Celiac Disease: Expert Review.
Green PHR, Paski S, Ko CW, Rubio-Tapia A. Green PHR, et al. Gastroenterology. 2022 Nov;163(5):1461-1469. doi: 10.1053/j.gastro.2022.07.086. Epub 2022 Sep 19. Gastroenterology. 2022. PMID: 36137844 Review.
If villous atrophy persists or the initial diagnosis of celiac disease was not confirmed, consider other causes of villous atrophy, including common variable immunodeficiency, autoimmune enteropathy, tropical sprue, and medication-induced enteropathy. ...BEST …
If villous atrophy persists or the initial diagnosis of celiac disease was not confirmed, consider other causes of villous atrophy, includin …
British Lung Foundation/United Kingdom Primary Immunodeficiency Network Consensus Statement on the Definition, Diagnosis, and Management of Granulomatous-Lymphocytic Interstitial Lung Disease in Common Variable Immunodeficiency Disorders.
Hurst JR, Verma N, Lowe D, Baxendale HE, Jolles S, Kelleher P, Longhurst HJ, Patel SY, Renzoni EA, Sander CR, Avery GR, Babar JL, Buckland MS, Burns S, Egner W, Gompels MM, Gordins P, Haddock JA, Hart SP, Hayman GR, Herriot R, Hoyles RK, Huissoon AP, Jacob J, Nicholson AG, Rassl DM, Sargur RB, Savic S, Seneviratne SL, Sheaff M, Vaitla PM, Walters GI, Whitehouse JL, Wright PA, Condliffe AM. Hurst JR, et al. J Allergy Clin Immunol Pract. 2017 Jul-Aug;5(4):938-945. doi: 10.1016/j.jaip.2017.01.021. Epub 2017 Mar 25. J Allergy Clin Immunol Pract. 2017. PMID: 28351785 Free article. Review.
A proportion of people living with common variable immunodeficiency disorders develop granulomatous-lymphocytic interstitial lung disease (GLILD). ...There was 100% agreement (score, 0.92 0.19) for the following definition: "GLILD is a distinct clinico-radio- …
A proportion of people living with common variable immunodeficiency disorders develop granulomatous-lymphocytic interst …
201 results