Search Page
Save citations to file
Email citations
Send citations to clipboard
Add to Collections
Add to My Bibliography
Create a file for external citation management software
Your saved search
Your RSS Feed
Filters
Results by year
Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
2009 | 1 |
2010 | 1 |
2011 | 2 |
2014 | 1 |
2024 | 0 |
Search Results
5 results
Results by year
Filters applied: . Clear all
Page 1
Burden of copy number variation in common variable immunodeficiency.
Clin Exp Immunol. 2014 Jul;177(1):269-71. doi: 10.1111/cei.12255.
Clin Exp Immunol. 2014.
PMID: 24329717
Free PMC article.
Congenital alterations of NEMO glutamic acid 223 result in hypohidrotic ectodermal dysplasia and immunodeficiency with normal serum IgG levels.
Karamchandani-Patel G, Hanson EP, Saltzman R, Kimball CE, Sorensen RU, Orange JS.
Karamchandani-Patel G, et al.
Ann Allergy Asthma Immunol. 2011 Jul;107(1):50-6. doi: 10.1016/j.anai.2011.03.009. Epub 2011 May 4.
Ann Allergy Asthma Immunol. 2011.
PMID: 21704885
Free PMC article.
Item in Clipboard
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.
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.
Item in Clipboard
A novel missense mutation in the nuclear factor-κB essential modulator (NEMO) gene resulting in impaired activation of the NF-κB pathway and a unique clinical phenotype presenting as MRSA subdural empyema.
Devora GA, Sun L, Chen Z, van Oers NS, Hanson EP, Orange JS, de la Morena MT.
Devora GA, et al.
J Clin Immunol. 2010 Nov;30(6):881-5. doi: 10.1007/s10875-010-9445-y. Epub 2010 Jul 23.
J Clin Immunol. 2010.
PMID: 20652730
Free PMC article.
Item in Clipboard
Comèl-Netherton syndrome defined as primary immunodeficiency.
Renner ED, Hartl D, Rylaarsdam S, Young ML, Monaco-Shawver L, Kleiner G, Markert ML, Stiehm ER, Belohradsky BH, Upton MP, Torgerson TR, Orange JS, Ochs HD.
Renner ED, et al.
J Allergy Clin Immunol. 2009 Sep;124(3):536-43. doi: 10.1016/j.jaci.2009.06.009. Epub 2009 Aug 14.
J Allergy Clin Immunol. 2009.
PMID: 19683336
Free PMC article.
Item in Clipboard
Cite
Cite