Davis J - Search Results

1

Intermediate phenotypes in patients with autosomal dominant hyper-IgE syndrome caused by somatic mosaicism.

Hsu AP, Sowerwine KJ, Lawrence MG, Davis J, Henderson CJ, Zarember KA, Garofalo M, Gallin JI, Kuhns DB, Heller T, Milner JD, Puck JM, Freeman AF, Holland SM. Hsu AP, et al. Among authors: davis j. J Allergy Clin Immunol. 2013 Jun;131(6):1586-93. doi: 10.1016/j.jaci.2013.02.038. Epub 2013 Apr 25. J Allergy Clin Immunol. 2013. PMID: 23623265 Free PMC article.

2

Genetic linkage of hyper-IgE syndrome to chromosome 4.

Grimbacher B, Schäffer AA, Holland SM, Davis J, Gallin JI, Malech HL, Atkinson TP, Belohradsky BH, Buckley RH, Cossu F, Español T, Garty BZ, Matamoros N, Myers LA, Nelson RP, Ochs HD, Renner ED, Wellinghausen N, Puck JM. Grimbacher B, et al. Among authors: davis j. Am J Hum Genet. 1999 Sep;65(3):735-44. doi: 10.1086/302547. Am J Hum Genet. 1999. PMID: 10441580 Free PMC article.

3

Genetic testing and screening in pediatric populations.

Davis J, Krasnewich D, Puck JM. Davis J, et al. Nurs Clin North Am. 2000 Sep;35(3):643-51. Nurs Clin North Am. 2000. PMID: 10957679 Review.

4

Sib understanding of genetics and attitudes toward carrier testing for X-linked severe combined immunodeficiency.

Fanos JH, Davis J, Puck JM. Fanos JH, et al. Among authors: davis j. Am J Med Genet. 2001 Jan 1;98(1):46-56. Am J Med Genet. 2001. PMID: 11426455

5

Pleiotropic defects in lymphocyte activation caused by caspase-8 mutations lead to human immunodeficiency.

Chun HJ, Zheng L, Ahmad M, Wang J, Speirs CK, Siegel RM, Dale JK, Puck J, Davis J, Hall CG, Skoda-Smith S, Atkinson TP, Straus SE, Lenardo MJ. Chun HJ, et al. Among authors: davis j. Nature. 2002 Sep 26;419(6905):395-9. doi: 10.1038/nature01063. Nature. 2002. PMID: 12353035

6

Autosomal recessive hyperimmunoglobulin E syndrome: a distinct disease entity.

Renner ED, Puck JM, Holland SM, Schmitt M, Weiss M, Frosch M, Bergmann M, Davis J, Belohradsky BH, Grimbacher B. Renner ED, et al. Among authors: davis j. J Pediatr. 2004 Jan;144(1):93-9. doi: 10.1016/S0022-3476(03)00449-9. J Pediatr. 2004. PMID: 14722525

7

Familial immunodeficiency with cutaneous vasculitis, myoclonus, and cognitive impairment.

Hay BN, Martin JE, Karp B, Davis J, Darnell D, Solomon B, Turner M, Holland SM, Puck JM. Hay BN, et al. Among authors: davis j. Am J Med Genet A. 2004 Mar 1;125A(2):145-51. doi: 10.1002/ajmg.a.20595. Am J Med Genet A. 2004. PMID: 14981714

8

Dermatitis and the newborn rash of hyper-IgE syndrome.

Eberting CL, Davis J, Puck JM, Holland SM, Turner ML. Eberting CL, et al. Among authors: davis j. Arch Dermatol. 2004 Sep;140(9):1119-25. doi: 10.1001/archderm.140.9.1119. Arch Dermatol. 2004. PMID: 15381553 Review.

9

Use of mycophenolate mofetil for chronic, refractory immune cytopenias in children with autoimmune lymphoproliferative syndrome.

Rao VK, Dugan F, Dale JK, Davis J, Tretler J, Hurley JK, Fleisher T, Puck J, Straus SE. Rao VK, et al. Among authors: davis j. Br J Haematol. 2005 May;129(4):534-8. doi: 10.1111/j.1365-2141.2005.05496.x. Br J Haematol. 2005. PMID: 15877736 Free article. Clinical Trial.

10

HLA B44 is associated with decreased severity of autoimmune lymphoproliferative syndrome in patients with CD95 defects (ALPS type Ia).

Vacek MM, Schäffer AA, Davis J, Fischer RE, Dale JK, Adams S, Straus SE, Puck JM. Vacek MM, et al. Among authors: davis j. Clin Immunol. 2006 Jan;118(1):59-65. doi: 10.1016/j.clim.2005.09.006. Epub 2005 Oct 27. Clin Immunol. 2006. PMID: 16257267

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