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Quoted phrase not found in phrase index: "Hyper-IgM syndrome type 3"
Page 1
Study of patients with Hyper-IgM type IV phenotype who recovered spontaneously during late childhood and review of the literature.
Karaca NE, Durandy A, Gulez N, Aksu G, Kutukculer N. Karaca NE, et al. Eur J Pediatr. 2011 Aug;170(8):1039-47. doi: 10.1007/s00431-011-1400-2. Epub 2011 Jan 28. Eur J Pediatr. 2011. PMID: 21274562 Review.
Hyper-IgM syndromes are characterized by normal or elevated serum IgM levels with the absence or reduced levels of other immunoglobulins. ...CONCLUSION: Clinical manifestations and immunoglobulin levels of the patients with Hyper-IgM type …
Hyper-IgM syndromes are characterized by normal or elevated serum IgM levels with the absence or reduced levels of othe …
Female hyper IgM syndrome type 1 with a chromosomal translocation disrupting CD40LG.
Imai K, Shimadzu M, Kubota T, Morio T, Matsunaga T, Park YD, Yoshioka A, Nonoyama S. Imai K, et al. Biochim Biophys Acta. 2006 Mar;1762(3):335-40. doi: 10.1016/j.bbadis.2005.10.003. Epub 2005 Oct 28. Biochim Biophys Acta. 2006. PMID: 16311023 Free article.
Hyper-IgM syndrome type 1 (HIGM1) is a primary immunodeficiency characterized by recurrent bacterial and opportunistic infections, associated with normal or high serum level of IgM and decreased serum levels of IgG, IgA and IgE due to the …
Hyper-IgM syndrome type 1 (HIGM1) is a primary immunodeficiency characterized by recurrent bacterial and …
Partial immune reconstitution of X-linked hyper IgM syndrome with recombinant CD40 ligand.
Jain A, Kovacs JA, Nelson DL, Migueles SA, Pittaluga S, Fanslow W, Fan X, Wong DW, Massey J, Hornung R, Brown MR, Spinner JJ, Liu S, Davey V, Hill HA, Ochs H, Fleisher TA. Jain A, et al. Blood. 2011 Oct 6;118(14):3811-7. doi: 10.1182/blood-2011-04-351254. Epub 2011 Aug 12. Blood. 2011. PMID: 21841160 Free PMC article. Clinical Trial.
X-linked hyper IgM syndrome (XHM) is a combined immune deficiency disorder caused by genetic alterations in CD40 ligand. ...Although specific antibody responses to T cell-dependent antigens was lacking, administration of rCD40 resulted in acquisition of the c …
X-linked hyper IgM syndrome (XHM) is a combined immune deficiency disorder caused by genetic alterations in CD40 ligand …
Immunologic reconstitution following bone marrow transplantation for X-linked hyper IgM syndrome.
Duplantier JE, Seyama K, Day NK, Hitchcock R, Nelson RP Jr, Ochs HD, Haraguchi S, Klemperer MR, Good RA. Duplantier JE, et al. Clin Immunol. 2001 Mar;98(3):313-8. doi: 10.1006/clim.2000.4994. Clin Immunol. 2001. PMID: 11237554
X-linked hyper IgM syndrome (XHIM), caused by mutations of the CD40 ligand (CD40L) gene, is characterized by recurrent bacterial and opportunistic infections, an increased incidence of autoimmunity and malignancies, and immunodeficiency due to abnormal …
X-linked hyper IgM syndrome (XHIM), caused by mutations of the CD40 ligand (CD40L) gene, is characterized by recurrent …
Clinical manifestations and outcomes of pediatric chronic neutropenia.
Wan C, Yu HH, Lu MY, Lee JH, Wang LC, Lin YT, Yang YH, Chiang BL. Wan C, et al. J Formos Med Assoc. 2012 Apr;111(4):220-7. doi: 10.1016/j.jfma.2010.12.003. Epub 2012 Mar 16. J Formos Med Assoc. 2012. PMID: 22526211 Free article.
Three CNS patients had severe chronic neutropenia, one had the Chediak-Higashi syndrome, one had the hyper-IgM syndrome, one had the glycogen storage disease type Ib, and one had the Barth syndrome. ...
Three CNS patients had severe chronic neutropenia, one had the Chediak-Higashi syndrome, one had the hyper-IgM syndr …
Hematopoietic Stem Cell Transplantation for CD40 Ligand Deficiency: Single Institution Experience.
Allewelt H, Martin PL, Szabolcs P, Chao N, Buckley R, Parikh S. Allewelt H, et al. Pediatr Blood Cancer. 2015 Dec;62(12):2216-22. doi: 10.1002/pbc.25711. Epub 2015 Aug 20. Pediatr Blood Cancer. 2015. PMID: 26291959 Clinical Trial.
BACKGROUND: X-linked hyper-IgM syndrome (X-HIGM) due to mutations in the gene encoding CD40 ligand results in failure of Ig class switching and an increased propensity for recurrent sinopulmonary and other infections, and thus decreased life expectancy. ...PR …
BACKGROUND: X-linked hyper-IgM syndrome (X-HIGM) due to mutations in the gene encoding CD40 ligand results in failure o …
Autoimmune retinopathy with RPE hypersensitivity and 'negative ERG' in X-linked hyper-IgM syndrome.
Schuster A, Apfelstedt-Sylla E, Pusch CM, Zrenner E, Thirkill CE. Schuster A, et al. Ocul Immunol Inflamm. 2005 Apr-Jun;13(2-3):235-43. doi: 10.1080/09273940590928571. Ocul Immunol Inflamm. 2005. PMID: 16019685
PURPOSE: To report the clinical, electrophysiological, and immunological features of a patient with X-linked hyper-IgM immunodeficiency syndrome type 1 (HIGM1) accompanied by a novel type of autoimmune retinopathy, including retinal pigme …
PURPOSE: To report the clinical, electrophysiological, and immunological features of a patient with X-linked hyper-IgM immu …
Allogeneic hematopoietic stem cell transplantation for seven children with X-linked hyper-IgM syndrome: a single center experience.
Tomizawa D, Imai K, Ito S, Kajiwara M, Minegishi Y, Nagasawa M, Morio T, Nonoyama S, Mizutani S. Tomizawa D, et al. Am J Hematol. 2004 May;76(1):33-9. doi: 10.1002/ajh.20044. Am J Hematol. 2004. PMID: 15114594 Free article.
X-linked hyper-IgM syndrome (XHIM), or hyper-IgM syndrome type 1 (HIGM1), is a rare primary immunodeficiency disorder susceptible to recurrent bacterial infection and opportunistic infection such as Pneumocystis carinii and …
X-linked hyper-IgM syndrome (XHIM), or hyper-IgM syndrome type 1 (HIGM1), is a rare primary …
AA Amyloidosis Secondary to Primary Immune Deficiency: About 40 Cases Including 2 New French Cases and a Systematic Literature Review.
Delplanque M, Galicier L, Oziol E, Ducharme-Bénard S, Oksenhendler E, Buob D, Grateau G, Boutboul D, Georgin-Lavialle S. Delplanque M, et al. J Allergy Clin Immunol Pract. 2021 Feb;9(2):745-752.e1. doi: 10.1016/j.jaip.2020.09.023. Epub 2020 Sep 30. J Allergy Clin Immunol Pract. 2021. PMID: 33007500
PIDs were varied: immunoglobulin deficits (n = 30), chronic granulomatous disease (n = 3), hyper-IgM syndrome (n = 3), hereditary complete C4 deficiency (n = 1), leucocyte adhesion deficiency type 1 (n = 1), hyper-IgE syndrome (n = 1), an …
PIDs were varied: immunoglobulin deficits (n = 30), chronic granulomatous disease (n = 3), hyper-IgM syndrome (n = 3), …
FATAL cryptococcal meningitis in a child with hyper-immunoglobulin M syndrome, with an emphasis on the agent.
Suzuki SML, Morelli F, Negri M, Bonfim-Mendonça P, Kioshima ÉS, Salci T, Voidaleski MF, Vicente VA, Svidzinski T. Suzuki SML, et al. J Mycol Med. 2019 Sep;29(3):273-277. doi: 10.1016/j.mycmed.2019.07.002. Epub 2019 Jul 26. J Mycol Med. 2019. PMID: 31409527
Following a fatal case of Cryptococcus neoformans meningitis in a child with X-linked hyper-immunoglobulin M syndrome (XHIGM), we evaluated the fungal isolate in an experimental infection in a mouse model with respect to microbiology, epidemiology, virulence and res …
Following a fatal case of Cryptococcus neoformans meningitis in a child with X-linked hyper-immunoglobulin M syndrome (XHIGM), …
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