These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
209 related articles for article (PubMed ID: 11583829)
1. Common variable immunodeficiency (CVID) in a family: an autosomal dominant mode of inheritance. Nijenhuis T; Klasen I; Weemaes CM; Preijers F; de Vries E; van der Meer JW Neth J Med; 2001 Sep; 59(3):134-9. PubMed ID: 11583829 [TBL] [Abstract][Full Text] [Related]
2. Linkage of autosomal-dominant common variable immunodeficiency to chromosome 4q. Finck A; Van der Meer JW; Schäffer AA; Pfannstiel J; Fieschi C; Plebani A; Webster AD; Hammarström L; Grimbacher B Eur J Hum Genet; 2006 Jul; 14(7):867-75. PubMed ID: 16639407 [TBL] [Abstract][Full Text] [Related]
3. Comparison of clinical and immunological features and mortality in common variable immunodeficiency and agammaglobulinemia patients. Bagheri Y; Vosughi A; Azizi G; Yazdani R; Kiaee F; Hafezi N; Alimorad S; Khoshmirsafa M; Seif F; Hassanpour G; Abolhassani H; Aghamohammadi A Immunol Lett; 2019 Jun; 210():55-62. PubMed ID: 31059734 [TBL] [Abstract][Full Text] [Related]
8. Late-onset combined immune deficiency: a subset of common variable immunodeficiency with severe T cell defect. Malphettes M; Gérard L; Carmagnat M; Mouillot G; Vince N; Boutboul D; Bérezné A; Nove-Josserand R; Lemoing V; Tetu L; Viallard JF; Bonnotte B; Pavic M; Haroche J; Larroche C; Brouet JC; Fermand JP; Rabian C; Fieschi C; Oksenhendler E; Clin Infect Dis; 2009 Nov; 49(9):1329-38. PubMed ID: 19807277 [TBL] [Abstract][Full Text] [Related]
9. Analysis of a family containing three members with common variable immunodeficiency. de Asis ML; Iqbal S; Sicklick M Ann Allergy Asthma Immunol; 1996 Jun; 76(6):527-9. PubMed ID: 8673687 [TBL] [Abstract][Full Text] [Related]
10. Alterations of the X-linked lymphoproliferative disease gene SH2D1A in common variable immunodeficiency syndrome. Morra M; Silander O; Calpe S; Choi M; Oettgen H; Myers L; Etzioni A; Buckley R; Terhorst C Blood; 2001 Sep; 98(5):1321-5. PubMed ID: 11520777 [TBL] [Abstract][Full Text] [Related]
11. Human ICOS deficiency abrogates the germinal center reaction and provides a monogenic model for common variable immunodeficiency. Warnatz K; Bossaller L; Salzer U; Skrabl-Baumgartner A; Schwinger W; van der Burg M; van Dongen JJ; Orlowska-Volk M; Knoth R; Durandy A; Draeger R; Schlesier M; Peter HH; Grimbacher B Blood; 2006 Apr; 107(8):3045-52. PubMed ID: 16384931 [TBL] [Abstract][Full Text] [Related]
12. Activating PI3Kδ mutations in a cohort of 669 patients with primary immunodeficiency. Elgizouli M; Lowe DM; Speckmann C; Schubert D; Hülsdünker J; Eskandarian Z; Dudek A; Schmitt-Graeff A; Wanders J; Jørgensen SF; Fevang B; Salzer U; Nieters A; Burns S; Grimbacher B Clin Exp Immunol; 2016 Feb; 183(2):221-9. PubMed ID: 26437962 [TBL] [Abstract][Full Text] [Related]
13. Exclusion of Patients with a Severe T-Cell Defect Improves the Definition of Common Variable Immunodeficiency. Bertinchamp R; Gérard L; Boutboul D; Malphettes M; Fieschi C; Oksenhendler E; J Allergy Clin Immunol Pract; 2016; 4(6):1147-1157. PubMed ID: 27522107 [TBL] [Abstract][Full Text] [Related]
14. Multiorgan infiltration by CD8+ T cells and 1p;16p translocation in a patient with hypogammaglobulinemia and a reduced number of B cells. Vultaggio A; Matucci A; D'Elios MM; Andreucci E; Giglio S; Annunziato F; Zupo S; Maggi E Int Arch Allergy Immunol; 2012; 158(2):206-10. PubMed ID: 22286841 [TBL] [Abstract][Full Text] [Related]
15. [Transient hypogammaglobulinemia of infancy]. Bellutti Enders F; Conti F; Candotti F; Angelini F Rev Med Suisse; 2017 Apr; 13(557):739-742. PubMed ID: 28722362 [TBL] [Abstract][Full Text] [Related]
16. A novel compound heterozygous TACI mutation in an autosomal recessive common variable immunodeficiency (CVID) family. Lougaris V; Gallizzi R; Vitali M; Baronio M; Salpietro A; Bergbreiter A; Salzer U; Badolato R; Plebani A Hum Immunol; 2012 Aug; 73(8):836-9. PubMed ID: 22627058 [TBL] [Abstract][Full Text] [Related]
17. [Immunological investigation of hypogammaglobulinemia]. Jureen R; Ulvestad E Tidsskr Nor Laegeforen; 1999 Mar; 119(7):940-3. PubMed ID: 10210954 [TBL] [Abstract][Full Text] [Related]
18. The immunophenotypic fingerprint of patients with primary antibody deficiencies is partially present in their asymptomatic first-degree relatives. Bogaert DJ; De Bruyne M; Debacker V; Depuydt P; De Preter K; Bonroy C; Philippé J; Bordon V; Lambrecht BN; Kerre T; Cerutti A; Vermaelen KY; Haerynck F; Dullaers M Haematologica; 2017 Jan; 102(1):192-202. PubMed ID: 27634199 [TBL] [Abstract][Full Text] [Related]
19. Keeping it in the family: the case for considering late-onset combined immunodeficiency a subset of common variable immunodeficiency disorders. Ameratunga R; Ahn Y; Jordan A; Lehnert K; Brothers S; Woon ST Expert Rev Clin Immunol; 2018 Jul; 14(7):549-556. PubMed ID: 29806948 [TBL] [Abstract][Full Text] [Related]
20. The Significance of B-cell Subsets in Patients with Unclassified Hypogammaglobulinemia and Association with Intravenous Immunoglobulin Replacement Requirement. Karaman S; Erdem SB; Gülez N; Genel F Iran J Immunol; 2018 Mar; 15(1):1-13. PubMed ID: 29549228 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]