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Page 1
Immunodeficiency in patients with 49,XXXXY chromosomal variation.
Keller MD, Sadeghin T, Samango-Sprouse C, Orange JS. Keller MD, et al. Among authors: orange js. Am J Med Genet C Semin Med Genet. 2013 Feb 15;163C(1):50-4. doi: 10.1002/ajmg.c.31348. Epub 2013 Jan 23. Am J Med Genet C Semin Med Genet. 2013. PMID: 23345259 Free PMC article.
Severe combined immunodeficiency resulting from mutations in MTHFD1.
Keller MD, Ganesh J, Heltzer M, Paessler M, Bergqvist AG, Baluarte HJ, Watkins D, Rosenblatt DS, Orange JS. Keller MD, et al. Among authors: orange js. Pediatrics. 2013 Feb;131(2):e629-34. doi: 10.1542/peds.2012-0899. Epub 2013 Jan 6. Pediatrics. 2013. PMID: 23296427
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: orange js. Clin Exp Immunol. 2014 Jul;177(1):269-71. doi: 10.1111/cei.12255. Clin Exp Immunol. 2014. PMID: 24329717 Free PMC article.
Practice parameter for the diagnosis and management of primary immunodeficiency.
Bonilla FA, Khan DA, Ballas ZK, Chinen J, Frank MM, Hsu JT, Keller M, Kobrynski LJ, Komarow HD, Mazer B, Nelson RP Jr, Orange JS, Routes JM, Shearer WT, Sorensen RU, Verbsky JW, Bernstein DI, Blessing-Moore J, Lang D, Nicklas RA, Oppenheimer J, Portnoy JM, Randolph CR, Schuller D, Spector SL, Tilles S, Wallace D; Joint Task Force on Practice Parameters, representing the American Academy of Allergy, Asthma & Immunology; the American College of Allergy, Asthma & Immunology; and the Joint Council of Allergy, Asthma & Immunology. Bonilla FA, et al. Among authors: orange js. J Allergy Clin Immunol. 2015 Nov;136(5):1186-205.e1-78. doi: 10.1016/j.jaci.2015.04.049. Epub 2015 Sep 12. J Allergy Clin Immunol. 2015. PMID: 26371839
Adoptive immunotherapy for primary immunodeficiency disorders with virus-specific T lymphocytes.
Naik S, Nicholas SK, Martinez CA, Leen AM, Hanley PJ, Gottschalk SM, Rooney CM, Hanson IC, Krance RA, Shpall EJ, Cruz CR, Amrolia P, Lucchini G, Bunin N, Heimall J, Klein OR, Gennery AR, Slatter MA, Vickers MA, Orange JS, Heslop HE, Bollard CM, Keller MD. Naik S, et al. Among authors: orange js. J Allergy Clin Immunol. 2016 May;137(5):1498-1505.e1. doi: 10.1016/j.jaci.2015.12.1311. Epub 2016 Feb 24. J Allergy Clin Immunol. 2016. PMID: 26920464 Free PMC article.
Mutation in IRF2BP2 is responsible for a familial form of common variable immunodeficiency disorder.
Keller MD, Pandey R, Li D, Glessner J, Tian L, Henrickson SE, Chinn IK, Monaco-Shawver L, Heimall J, Hou C, Otieno FG, Jyonouchi S, Calabrese L, van Montfrans J, Orange JS, Hakonarson H. Keller MD, et al. Among authors: orange js. J Allergy Clin Immunol. 2016 Aug;138(2):544-550.e4. doi: 10.1016/j.jaci.2016.01.018. Epub 2016 Mar 23. J Allergy Clin Immunol. 2016. PMID: 27016798 Free PMC article.
375 results