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Page 1
Deconstructing common variable immunodeficiency by genetic analysis.
Schäffer AA, Salzer U, Hammarström L, Grimbacher B. Schäffer AA, et al. Among authors: hammarstrom l. Curr Opin Genet Dev. 2007 Jun;17(3):201-12. doi: 10.1016/j.gde.2007.04.002. Epub 2007 Apr 27. Curr Opin Genet Dev. 2007. PMID: 17467261 Review.
ICOS deficiency in patients with common variable immunodeficiency.
Salzer U, Maul-Pavicic A, Cunningham-Rundles C, Urschel S, Belohradsky BH, Litzman J, Holm A, Franco JL, Plebani A, Hammarstrom L, Skrabl A, Schwinger W, Grimbacher B. Salzer U, et al. Among authors: hammarstrom l. Clin Immunol. 2004 Dec;113(3):234-40. doi: 10.1016/j.clim.2004.07.002. Clin Immunol. 2004. PMID: 15507387
Linkage of autosomal-dominant common variable immunodeficiency to chromosome 4q.
Finck A, Van der Meer JW, Schäffer AA, Pfannstiel J, Fieschi C, Plebani A, Webster AD, Hammarström L, Grimbacher B. Finck A, et al. Among authors: hammarstrom l. Eur J Hum Genet. 2006 Jul;14(7):867-75. doi: 10.1038/sj.ejhg.5201634. Epub 2006 Apr 26. Eur J Hum Genet. 2006. PMID: 16639407
Reexamining the role of TACI coding variants in common variable immunodeficiency and selective IgA deficiency.
Pan-Hammarström Q, Salzer U, Du L, Björkander J, Cunningham-Rundles C, Nelson DL, Bacchelli C, Gaspar HB, Offer S, Behrens TW, Grimbacher B, Hammarström L. Pan-Hammarström Q, et al. Among authors: hammarstrom l. Nat Genet. 2007 Apr;39(4):429-30. doi: 10.1038/ng0407-429. Nat Genet. 2007. PMID: 17392797 Free PMC article. No abstract available.
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, Metin A, Webster DA, Plebani A, Moschese V, Hammarström L, Schäffer AA, Grimbacher B. Salzer U, et al. Among authors: hammarstrom l. BMC Immunol. 2008 Feb 7;9:3. doi: 10.1186/1471-2172-9-3. BMC Immunol. 2008. PMID: 18254984 Free PMC article.
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, Webster AD, Peter HH, Suez D, Chapel H, McLean-Tooke A, Spickett GP, Anover-Sombke S, Ochs HD, Urschel S, Belohradsky BH, Ugrinovic S, Kumararatne DS, Lawrence TC, Holm AM, Franco JL, Schulze I, Schneider P, Gertz EM, Schäffer AA, Hammarström L, Thrasher AJ, Gaspar HB, Grimbacher B. Salzer U, et al. Among authors: hammarstrom l. Blood. 2009 Feb 26;113(9):1967-76. doi: 10.1182/blood-2008-02-141937. Epub 2008 Nov 3. Blood. 2009. PMID: 18981294 Free PMC article.
Novel mutations in TACI (TNFRSF13B) causing common variable immunodeficiency.
Mohammadi J, Liu C, Aghamohammadi A, Bergbreiter A, Du L, Lu J, Rezaei N, Amirzargar AA, Moin M, Salzer U, Pan-Hammarström Q, Hammarström L. Mohammadi J, et al. Among authors: hammarstrom l. J Clin Immunol. 2009 Nov;29(6):777-85. doi: 10.1007/s10875-009-9317-5. Epub 2009 Jul 23. J Clin Immunol. 2009. PMID: 19629655
1,049 results