Sullivan KE - Search Results

1

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.

2

Sarcoidosis and common variable immunodeficiency. Report of 8 cases and review of the literature.

Fasano MB, Sullivan KE, Sarpong SB, Wood RA, Jones SM, Johns CJ, Lederman HM, Bykowsky MJ, Greene JM, Winkelstein JA. Fasano MB, et al. Among authors: sullivan ke. Medicine (Baltimore). 1996 Sep;75(5):251-61. doi: 10.1097/00005792-199609000-00002. Medicine (Baltimore). 1996. PMID: 8862347 Free article. Review.

3

Serum complement determinations in patients with quiescent systemic lupus erythematosus.

Sullivan KE, Wisnieski JJ, Winkelstein JA, Louie J, Sachs E, Choi R, Veksler E, Goldman D, Petri M. Sullivan KE, et al. J Rheumatol. 1996 Dec;23(12):2063-7. J Rheumatol. 1996. PMID: 8970042

4

Cell cycle checkpoints and DNA repair in Nijmegen breakage syndrome.

Sullivan KE, Veksler E, Lederman H, Lees-Miller SP. Sullivan KE, et al. Clin Immunol Immunopathol. 1997 Jan;82(1):43-8. doi: 10.1006/clin.1996.4275. Clin Immunol Immunopathol. 1997. PMID: 9000041 Free article.

5

Adenosine deaminase deficiency and purine nucleoside phosphorylase deficiency in common variable immunodeficiency.

Fleischman A, Hershfield MS, Toutain S, Lederman HM, Sullivan KE, Fasano MB, Greene J, Winkelstein JA. Fleischman A, et al. Among authors: sullivan ke. Clin Diagn Lab Immunol. 1998 May;5(3):399-400. doi: 10.1128/CDLI.5.3.399-400.1998. Clin Diagn Lab Immunol. 1998. PMID: 9605997 Free PMC article.

6

Cytokine and chemokine dysregulation in hyper-IgE syndrome.

Chehimi J, Elder M, Greene J, Noroski L, Stiehm ER, Winkelstein JA, Sullivan KE. Chehimi J, et al. Among authors: sullivan ke. Clin Immunol. 2001 Jul;100(1):49-56. doi: 10.1006/clim.2001.5039. Clin Immunol. 2001. PMID: 11414745

7

X-Linked Agammaglobulinemia: Infection Frequency and Infection-Related Mortality in the USIDNET Registry.

O'Toole D, Groth D, Wright H, Bonilla FA, Fuleihan RL, Cunningham-Rundles C, Sullivan KE, Ochs HD, Marsh R, Feuille E. O'Toole D, et al. Among authors: sullivan ke. J Clin Immunol. 2022 May;42(4):827-836. doi: 10.1007/s10875-022-01237-1. Epub 2022 Mar 15. J Clin Immunol. 2022. PMID: 35288819 Free PMC article.

8

Autosomal dominant "Opitz" GBBB syndrome due to a 22q11.2 deletion.

McDonald-McGinn DM, Driscoll DA, Bason L, Christensen K, Lynch D, Sullivan K, Canning D, Zavod W, Quinn N, Rome J. McDonald-McGinn DM, et al. Am J Med Genet. 1995 Oct 23;59(1):103-13. doi: 10.1002/ajmg.1320590122. Am J Med Genet. 1995. PMID: 8849001

9

3' polymorphisms of ETS1 are associated with different clinical phenotypes in SLE.

Sullivan KE, Piliero LM, Dharia T, Goldman D, Petri MA. Sullivan KE, et al. Hum Mutat. 2000;16(1):49-53. doi: 10.1002/1098-1004(200007)16:1<49::AID-HUMU9>3.0.CO;2-Z. Hum Mutat. 2000. PMID: 10874305

10

Immunologic features of chromosome 22q11.2 deletion syndrome (DiGeorge syndrome/velocardiofacial syndrome).

Jawad AF, McDonald-Mcginn DM, Zackai E, Sullivan KE. Jawad AF, et al. Among authors: sullivan ke. J Pediatr. 2001 Nov;139(5):715-23. doi: 10.1067/mpd.2001.118534. J Pediatr. 2001. PMID: 11713452

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