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7. Disseminated Histoplasma capsulatum in a patient with hyper IgM immunodeficiency. Hostoffer RW; Berger M; Clark HT; Schreiber JR Pediatrics; 1994 Aug; 94(2 Pt 1):234-6. PubMed ID: 8036080 [No Abstract] [Full Text] [Related]
8. Localization of the genetic defect in X-linked immunoglobulin deficiency with normal or elevated IgM (HIGMX-1) to the CD40 ligand gene. Fuleihan R; Ramesh N; Rosen FS; Geha RS Trans Assoc Am Physicians; 1993; 106():91-5. PubMed ID: 7518624 [No Abstract] [Full Text] [Related]
9. A familial case of hyper-IgM immunodeficiency. Iwakiri R; Nakano T; Harada M; Nagafuchi S; Teshima T; Ono N; Yamamoto Y; Niho Y Acta Haematol; 1992; 88(1):50-4. PubMed ID: 1414163 [TBL] [Abstract][Full Text] [Related]
10. Hyper-immunoglobulin M syndrome caused by a mutation in the promotor for CD40L. Van Hoeyveld E; Zhang PX; De Boeck K; Fuleihan R; Bossuyt X Immunology; 2007 Apr; 120(4):497-501. PubMed ID: 17244160 [TBL] [Abstract][Full Text] [Related]
11. Evidence for the failure of IgA specific T helper activity in a patient with immunodeficiency with hyper IgM. Mitsuya H; Tomino S; Hisamitsu S; Kishimoto S J Clin Lab Immunol; 1979 Nov; 2(4):337-42. PubMed ID: 317110 [TBL] [Abstract][Full Text] [Related]
12. The X-linked hyper-IgM syndrome: clinical and immunologic features of 79 patients. Winkelstein JA; Marino MC; Ochs H; Fuleihan R; Scholl PR; Geha R; Stiehm ER; Conley ME Medicine (Baltimore); 2003 Nov; 82(6):373-84. PubMed ID: 14663287 [TBL] [Abstract][Full Text] [Related]
13. Signaling through CD40 rescues IgE but not IgG or IgA secretion in X-linked immunodeficiency with hyper-IgM. Saiki O; Tanaka T; Wada Y; Uda H; Inoue A; Katada Y; Izeki M; Iwata M; Nunoi H; Matsuda I J Clin Invest; 1995 Feb; 95(2):510-4. PubMed ID: 7532185 [TBL] [Abstract][Full Text] [Related]
14. Human malignant T cells capable of inducing an immunoglobulin class switch. Mayer L; Posnett DN; Kunkel HG J Exp Med; 1985 Jan; 161(1):134-44. PubMed ID: 2981951 [TBL] [Abstract][Full Text] [Related]
15. CD40:CD40L interactions in X-linked and non-X-linked hyper-IgM syndromes. Bhushan A; Covey LR Immunol Res; 2001; 24(3):311-24. PubMed ID: 11817328 [TBL] [Abstract][Full Text] [Related]
16. Hyperimmunoglobulin syndrome due to CD40 deficiency: possibly the first case from India. Mishra A; Italia K; Gupta M; Desai M; Madkaikar M J Postgrad Med; 2015; 61(1):46-8. PubMed ID: 25511220 [TBL] [Abstract][Full Text] [Related]
17. Immunologic studies of three family members with the immunodeficiency with hyper-IgM syndrome. Brahmi Z; Lazarus KH; Hodes ME; Baehner RL J Clin Immunol; 1983 Apr; 3(2):127-34. PubMed ID: 6602145 [TBL] [Abstract][Full Text] [Related]
18. Familial variable immunodeficiency: autosomal dominant pattern of inheritance with variable expression of the defect(s). Feldman G; Koziner B; Talamo R; Bloch KJ J Pediatr; 1975 Oct; 87(4):534-9. PubMed ID: 1080516 [TBL] [Abstract][Full Text] [Related]
19. In vivo but not in vitro stimulations rescue of the defective class switching to IgG or IgA in B-cells of immunodeficiency with hyper IgM. Saiki O; Uda H; Hayashi M; Tanaka T; Katada Y; Shimizu M; Kinoshita N; Kishimoto T Clin Immunol Immunopathol; 1997 Jun; 83(3):287-92. PubMed ID: 9175918 [TBL] [Abstract][Full Text] [Related]
20. Assessment and clinical interpretation of reduced IgG values. Agarwal S; Cunningham-Rundles C Ann Allergy Asthma Immunol; 2007 Sep; 99(3):281-3. PubMed ID: 17910333 [No Abstract] [Full Text] [Related] [Next] [New Search]