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Volumn 42, Issue 5, 2010, Pages 194-196

Hyper-IgM Syndrome - A case report and a clinical perspective

Author keywords

AICDA; Hyper IgM; Hypogammaglobulinemia; Immunodeficiency; Immunoglobulin M

Indexed keywords

ACTIVATION INDUCED CYTIDINE DEAMINASE; ANTIBIOTIC AGENT; IMMUNOGLOBULIN;

EID: 77958562755     PISSN: 03979148     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article
Times cited : (5)

References (9)
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    • Primary immunodeficiency disorders: Antibody deficiency
    • DOI 10.1067/mai.2002.122466
    • Ballow M. Primary immunodeficiency disorders: antibody deficiency. J Allergy Clin Immunol 2002; 109(4):581-91. (Pubitemid 34327181)
    • (2002) Journal of Allergy and Clinical Immunology , vol.109 , Issue.4 , pp. 581-591
    • Ballow, M.1
  • 4
    • 0034264851 scopus 로고    scopus 로고
    • Activation-induced cytidine deaminase (AID) deficiency causes the autosomal recessive form of the Hyper-IgM syndrome (HIGM2)
    • Revy P, Muto T, Levy Y, et al. Activation-induced cytidine deaminase (AID) deficiency causes the autosomal recessive form of the Hyper-IgM syndrome (HIGM2). Cell 2000; 102:565-75.
    • (2000) Cell , vol.102 , pp. 565-575
    • Revy, P.1    Muto, T.2    Levy, Y.3
  • 5
    • 10744226125 scopus 로고    scopus 로고
    • Clinical, immunologic and genetic analysis of 29 patients with autosomal recessive hyper-IgM syndrome due to Activation-Induced Cytidine Deaminase deficiency
    • Quartier P, Bustamante J, Sanal O, et al. Clinical, immunologic and genetic analysis of 29 patients with autosomal recessive hyper-IgM syndrome due to Activation-Induced Cytidine Deaminase deficiency. Clin Immunol 2004; 110(1):22-9.
    • (2004) Clin Immunol , vol.110 , Issue.1 , pp. 22-29
    • Quartier, P.1    Bustamante, J.2    Sanal, O.3
  • 6
    • 0142092610 scopus 로고    scopus 로고
    • Human uracil-DNA glycosylase deficiency associated with profoundly impaired immunoglobulin class-switch recombination
    • Imai K, Slupphaug G, Lee WI, et al. Human uracil-DNA glycosylase deficiency associated with profoundly impaired immunoglobulin class-switch recombination.Nat Immunol 2003; 4(10):1023-8.
    • (2003) Nat Immunol , vol.4 , Issue.10 , pp. 1023-1028
    • Imai, K.1    Slupphaug, G.2    Lee, W.I.3
  • 7
    • 14944385521 scopus 로고    scopus 로고
    • Molecular analysis of a large cohort of patients with the hyper immunoglobulin M (IgM) syndrome
    • Lee WI, Torgerson TR, Schumacher MJ, et al. Molecular analysis of a large cohort of patients with the hyper immunoglobulin M (IgM) syndrome. Blood 2005; 105:1881-90.
    • (2005) Blood , vol.105 , pp. 1881-1890
    • Lee, W.I.1    Torgerson, T.R.2    Schumacher, M.J.3
  • 8
    • 72849145526 scopus 로고    scopus 로고
    • Clinical and Laboratory Findings in Hyper-IgM Syndrome with Novel CD40L and AICDA Mutations
    • Aghamohammadi A, Parvaneh N, Rezaei N, et al. Clinical and Laboratory Findings in Hyper-IgM Syndrome with Novel CD40L and AICDA Mutations. J Clin Immunol 2009; 29(6):769-76.
    • (2009) J Clin Immunol , vol.29 , Issue.6 , pp. 769-776
    • Aghamohammadi, A.1    Parvaneh, N.2    Rezaei, N.3
  • 9
    • 43449090386 scopus 로고    scopus 로고
    • Patients with abnormal IgM levels: Assessment, clinical interpretation, and treatment
    • Ochs HD. Patients with abnormal IgM levels: assessment, clinical interpretation, and treatment. Ann Allergy Asthma Immunol 2008; 100(5):509-11.
    • (2008) Ann Allergy Asthma Immunol , vol.100 , Issue.5 , pp. 509-511
    • Ochs, H.D.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.