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.
168 related articles for article (PubMed ID: 28805315)
1. A Comparison of Clinical and Immunologic Phenotypes in Familial and Sporadic Forms of Common Variable Immunodeficiency. Valizadeh A; Yazdani R; Azizi G; Abolhassani H; Aghamohammadi A Scand J Immunol; 2017 Oct; 86(4):239-247. PubMed ID: 28805315 [TBL] [Abstract][Full Text] [Related]
2. Familial inheritance and screening of first-degree relatives in common variable immunodeficiency and immunoglobulin A deficiency patients. Karaca NE; Severcan EU; Bilgin BG; Azarsiz E; Akarcan S; Gunaydın NC; Gulez N; Genel F; Aksu G; Kutukculer N Int J Immunopathol Pharmacol; 2018; 32():2058738418779458. PubMed ID: 29978731 [TBL] [Abstract][Full Text] [Related]
3. Phenotyping and follow up of forty-seven Iranian patients with common variable immunodeficiency. Arshi S; Nabavi M; Bemanian MH; Shakeri R; Taghvaei B; Ghalebaghi B; Babaie D; Bahrami A; Fallahpour M; Esmaeilzadeh H; Rekabi M; Amadian J; Eslami N; Shokri S; Jalali F; Akbarpour N; Molatefi R; Rezaei N Allergol Immunopathol (Madr); 2016; 44(3):226-31. PubMed ID: 26232306 [TBL] [Abstract][Full Text] [Related]
4. Correlation between common variable immunodeficiency clinical phenotypes and parental consanguinity in children and adults. Aghamohammadi A; Abolhassani H; Moazzami K; Parvaneh N; Rezaei N J Investig Allergol Clin Immunol; 2010; 20(5):372-9. PubMed ID: 20945602 [TBL] [Abstract][Full Text] [Related]
5. Mutation in IRF2BP2 is responsible for a familial form of common variable immunodeficiency disorder. Keller MD; Pandey R; Li D; Glessner J; Tian L; Henrickson SE; Chinn IK; Monaco-Shawver L; Heimall J; Hou C; Otieno FG; Jyonouchi S; Calabrese L; van Montfrans J; Orange JS; Hakonarson H J Allergy Clin Immunol; 2016 Aug; 138(2):544-550.e4. PubMed ID: 27016798 [TBL] [Abstract][Full Text] [Related]
10. Assessing the Functional Relevance of Variants in the Eskandarian Z; Fliegauf M; Bulashevska A; Proietti M; Hague R; Smulski CR; Schubert D; Warnatz K; Grimbacher B Front Immunol; 2019; 10():568. PubMed ID: 31057532 [TBL] [Abstract][Full Text] [Related]
11. 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]
13. Histocompatibility Complex Status and Mendelian Randomization Analysis in Unsolved Antibody Deficiency. Abolhassani H; Lim CK; Aghamohammadi A; Hammarström L Front Immunol; 2020; 11():14. PubMed ID: 32038658 [TBL] [Abstract][Full Text] [Related]
14. Clinical and immunologic features of pediatric patients with common variable immunodeficiency and respiratory complications. Aydogan M; Eifan AO; Gocmen I; Ozdemir C; Bahceciler NN; Barlan IB J Investig Allergol Clin Immunol; 2008; 18(4):260-5. PubMed ID: 18714533 [TBL] [Abstract][Full Text] [Related]
15. 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]
16. 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]
17. HLA-A and -B alleles and haplotypes in 240 index patients with common variable immunodeficiency and selective IgG subclass deficiency in central Alabama. Barton JC; Bertoli LF; Acton RT BMC Med Genet; 2003 Jun; 4():3. PubMed ID: 12803653 [TBL] [Abstract][Full Text] [Related]
18. Parental consanguinity is associated with a severe phenotype in common variable immunodeficiency. Rivoisy C; Gérard L; Boutboul D; Malphettes M; Fieschi C; Durieu I; Tron F; Masseau A; Bordigoni P; Alric L; Haroche J; Hoarau C; Bérézné A; Carmagnat M; Mouillot G; Oksenhendler E; J Clin Immunol; 2012 Feb; 32(1):98-105. PubMed ID: 22002594 [TBL] [Abstract][Full Text] [Related]
19. Common variable immunodeficiency: 20-yr experience at a single centre. Llobet MP; Soler-Palacin P; Detkova D; Hernández M; Caragol I; Espanol T Pediatr Allergy Immunol; 2009 Mar; 20(2):113-8. PubMed ID: 18798799 [TBL] [Abstract][Full Text] [Related]
20. Soluble CD26 and CD30 levels in patients with common variable immunodeficiency. Mahmoudi M; Hedayat M; Aghamohammadi A; Rezaei N J Investig Allergol Clin Immunol; 2013; 23(2):120-4. PubMed ID: 23654079 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]