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Discordant phenotype in siblings with X-linked agammaglobulinemia.
Bykowsky MJ, Haire RN, Ohta Y, Tang H, Sung SS, Veksler ES, Greene JM, Fu SM, Litman GW, Sullivan KE. Bykowsky MJ, et al. Among authors: sullivan ke. Am J Hum Genet. 1996 Mar;58(3):477-83. Am J Hum Genet. 1996. PMID: 8644706 Free PMC article.
Progressive neurodegeneration in patients with primary immunodeficiency disease on IVIG treatment.
Ziegner UH, Kobayashi RH, Cunningham-Rundles C, Español T, Fasth A, Huttenlocher A, Krogstad P, Marthinsen L, Notarangelo LD, Pasic S, Rieger CH, Rudge P, Sankar R, Shigeoka AO, Stiehm ER, Sullivan KE, Webster AD, Ochs HD. Ziegner UH, et al. Among authors: sullivan ke. Clin Immunol. 2002 Jan;102(1):19-24. doi: 10.1006/clim.2001.5140. Clin Immunol. 2002. PMID: 11781063
How to flee the flu.
Junker AK, Bonilla FA, Sullivan KE. Junker AK, et al. Among authors: sullivan ke. Clin Immunol. 2004 Sep;112(3):219-20. doi: 10.1016/j.clim.2004.03.013. Clin Immunol. 2004. PMID: 15308112 No abstract available.
Uncommon conundrum in common variable immunodeficiency.
Cunningham-Rundles C, Routes JM, Hostoffer R, Sullivan KE. Cunningham-Rundles C, et al. Among authors: sullivan ke. Clin Immunol. 2005 Sep;116(3):208-10. doi: 10.1016/j.clim.2005.04.006. Clin Immunol. 2005. PMID: 15905130 No abstract available.
An exemplum of XLA.
Notarangelo LD, Rawlings DJ, Sullivan KE. Notarangelo LD, et al. Among authors: sullivan ke. Clin Immunol. 2008 Feb;126(2):137-9. doi: 10.1016/j.clim.2007.09.003. Epub 2007 Oct 31. Clin Immunol. 2008. PMID: 17974484 No abstract available.
Improving cellular therapy for primary immune deficiency diseases: recognition, diagnosis, and management.
Griffith LM, Cowan MJ, Notarangelo LD, Puck JM, Buckley RH, Candotti F, Conley ME, Fleisher TA, Gaspar HB, Kohn DB, Ochs HD, O'Reilly RJ, Rizzo JD, Roifman CM, Small TN, Shearer WT; Workshop Participants. Griffith LM, et al. J Allergy Clin Immunol. 2009 Dec;124(6):1152-60.e12. doi: 10.1016/j.jaci.2009.10.022. J Allergy Clin Immunol. 2009. PMID: 20004776 Free PMC article.
Genome-wide association identifies diverse causes of common variable immunodeficiency.
Orange JS, Glessner JT, Resnick E, Sullivan KE, Lucas M, Ferry B, Kim CE, Hou C, Wang F, Chiavacci R, Kugathasan S, Sleasman JW, Baldassano R, Perez EE, Chapel H, Cunningham-Rundles C, Hakonarson H. Orange JS, et al. Among authors: sullivan ke. J Allergy Clin Immunol. 2011 Jun;127(6):1360-7.e6. doi: 10.1016/j.jaci.2011.02.039. Epub 2011 Apr 17. J Allergy Clin Immunol. 2011. PMID: 21497890 Free PMC article.
Primary Immune Deficiency Treatment Consortium (PIDTC) report.
Griffith LM, Cowan MJ, Notarangelo LD, Kohn DB, Puck JM, Pai SY, Ballard B, Bauer SC, Bleesing JJ, Boyle M, Brower A, Buckley RH, van der Burg M, Burroughs LM, Candotti F, Cant AJ, Chatila T, Cunningham-Rundles C, Dinauer MC, Dvorak CC, Filipovich AH, Fleisher TA, Bobby Gaspar H, Gungor T, Haddad E, Hovermale E, Huang F, Hurley A, Hurley M, Iyengar S, Kang EM, Logan BR, Long-Boyle JR, Malech HL, McGhee SA, Modell F, Modell V, Ochs HD, O'Reilly RJ, Parkman R, Rawlings DJ, Routes JM, Shearer WT, Small TN, Smith H, Sullivan KE, Szabolcs P, Thrasher A, Torgerson TR, Veys P, Weinberg K, Zuniga-Pflucker JC; workshop participants. Griffith LM, et al. Among authors: sullivan ke. J Allergy Clin Immunol. 2014 Feb;133(2):335-47. doi: 10.1016/j.jaci.2013.07.052. Epub 2013 Oct 15. J Allergy Clin Immunol. 2014. PMID: 24139498 Free PMC article.
Burden of copy number variation in common variable immunodeficiency.
Keller M, Glessner J, Resnick E, Perez E, Chapel H, Lucas M, Sullivan KE, Cunningham-Rundles C, Orange JS, Hakonarson H. Keller M, et al. Among authors: sullivan ke. Clin Exp Immunol. 2014 Jul;177(1):269-71. doi: 10.1111/cei.12255. Clin Exp Immunol. 2014. PMID: 24329717 Free PMC article.
414 results