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IgA deficiency.
Department of Microbiology, University of Alabama at Birmingham, USA.
PMID: 9238511 [PubMed - indexed for MEDLINE]
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Cited by 16 PubMed Central articles
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Relevance of biallelic versus monoallelic TNFRSF13B mutations in distinguishing disease-causing from risk-increasing TNFRSF13B variants in antibody deficiency syndromes.
Salzer U, Bacchelli C, Buckridge S, Pan-Hammarström Q, Jennings S, Lougaris V, Bergbreiter A, Hagena T, Birmelin J, Plebani A, et al.
Blood. 2009 Feb 26; 113(9):1967-76. Epub 2008 Nov 3.
[Blood. 2009]
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Screening of functional and positional candidate genes in families with common variable immunodeficiency.
Salzer U, Neumann C, Thiel J, Woellner C, Pan-Hammarström Q, Lougaris V, Hagena T, Jung J, Birmelin J, Du L, et al.
BMC Immunol. 2008 Feb 7; 9:3. Epub 2008 Feb 7.
[BMC Immunol. 2008]
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ReviewTranslational mini-review series on immunodeficiency: molecular defects in common variable immunodeficiency.
Bacchelli C, Buckridge S, Thrasher AJ, Gaspar HB.
Clin Exp Immunol. 2007 Sep; 149(3):401-9.
[Clin Exp Immunol. 2007]
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