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Items: 1 to 20 of 95

1.

Perspectives on common variable immune deficiency.

Park JH, Resnick ES, Cunningham-Rundles C.

Ann N Y Acad Sci. 2011 Dec;1246:41-9. doi: 10.1111/j.1749-6632.2011.06338.x. Review.

2.

"A rose is a rose is a rose," but CVID is Not CVID common variable immune deficiency (CVID), what do we know in 2011?

Yong PF, Thaventhiran JE, Grimbacher B.

Adv Immunol. 2011;111:47-107. doi: 10.1016/B978-0-12-385991-4.00002-7. Review.

PMID:
21970952
3.
4.

Translational mini-review series on immunodeficiency: molecular defects in common variable immunodeficiency.

Bacchelli C, Buckridge S, Thrasher AJ, Gaspar HB.

Clin Exp Immunol. 2007 Sep;149(3):401-9. Review.

5.

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.

J Allergy Clin Immunol. 2011 Jun;127(6):1360-7.e6. doi: 10.1016/j.jaci.2011.02.039. Epub 2011 Apr 17.

6.

Common variable immunodeficiency.

Takahashi N, Morio T.

Nihon Rinsho Meneki Gakkai Kaishi. 2008 Feb;31(1):9-16. Review.

7.

Understanding the genetic and epigenetic basis of common variable immunodeficiency disorder through omics approaches.

Li J, Wei Z, Li YR, Maggadottir SM, Chang X, Desai A, Hakonarson H.

Biochim Biophys Acta. 2016 Nov;1860(11 Pt B):2656-63. doi: 10.1016/j.bbagen.2016.06.014. Epub 2016 Jun 15. Review.

PMID:
27316315
8.

Human B cell defects in perspective.

Cunningham-Rundles C.

Immunol Res. 2012 Dec;54(1-3):227-32. doi: 10.1007/s12026-012-8318-2. Review.

9.

Rare variants at 16p11.2 are associated with common variable immunodeficiency.

Maggadottir SM, Li J, Glessner JT, Li YR, Wei Z, Chang X, Mentch FD, Thomas KA, Kim CE, Zhao Y, Hou C, Wang F, Jørgensen SF, Perez EE, Sullivan KE, Orange JS, Karlsen TH, Chapel H, Cunningham-Rundles C, Hakonarson H.

J Allergy Clin Immunol. 2015 Jun;135(6):1569-77. doi: 10.1016/j.jaci.2014.12.1939. Epub 2015 Feb 10.

10.

Common variable immunodeficiency: the immune system in chaos.

Bayry J, Hermine O, Webster DA, Lévy Y, Kaveri SV.

Trends Mol Med. 2005 Aug;11(8):370-6. Review.

PMID:
15996517
11.

Screening of functional and positional candidate genes in families with common variable immunodeficiency.

Salzer U, Neumann C, Thiel J, Woellner C, Pan-Hammarström Q, Lougaris V, Hagena T, Jung J, Birmelin J, Du L, Metin A, Webster DA, Plebani A, Moschese V, Hammarström L, Schäffer AA, Grimbacher B.

BMC Immunol. 2008 Feb 7;9:3. doi: 10.1186/1471-2172-9-3.

12.

Genetic defects in common variable immunodeficiency.

Kopecký O, Lukesová S.

Int J Immunogenet. 2007 Aug;34(4):225-9. Review.

13.

ICOS deficiency in patients with common variable immunodeficiency.

Salzer U, Maul-Pavicic A, Cunningham-Rundles C, Urschel S, Belohradsky BH, Litzman J, Holm A, Franco JL, Plebani A, Hammarstrom L, Skrabl A, Schwinger W, Grimbacher B.

Clin Immunol. 2004 Dec;113(3):234-40.

PMID:
15507387
14.

Genes associated with common variable immunodeficiency: one diagnosis to rule them all?

Bogaert DJ, Dullaers M, Lambrecht BN, Vermaelen KY, De Baere E, Haerynck F.

J Med Genet. 2016 Sep;53(9):575-90. doi: 10.1136/jmedgenet-2015-103690. Epub 2016 Jun 1. Review.

PMID:
27250108
15.

Linkage of autosomal-dominant common variable immunodeficiency to chromosome 4q.

Finck A, Van der Meer JW, Schäffer AA, Pfannstiel J, Fieschi C, Plebani A, Webster AD, Hammarström L, Grimbacher B.

Eur J Hum Genet. 2006 Jul;14(7):867-75. Epub 2006 Apr 26.

16.

The many faces of the clinical picture of common variable immune deficiency.

Resnick ES, Cunningham-Rundles C.

Curr Opin Allergy Clin Immunol. 2012 Dec;12(6):595-601. doi: 10.1097/ACI.0b013e32835914b9. Review.

PMID:
23026770
17.

A common single nucleotide polymorphism impairs B-cell activating factor receptor's multimerization, contributing to common variable immunodeficiency.

Pieper K, Rizzi M, Speletas M, Smulski CR, Sic H, Kraus H, Salzer U, Fiala GJ, Schamel WW, Lougaris V, Plebani A, Hammarstrom L, Recher M, Germenis AE, Grimbacher B, Warnatz K, Rolink AG, Schneider P, Notarangelo LD, Eibel H.

J Allergy Clin Immunol. 2014 Apr;133(4):1222-5. doi: 10.1016/j.jaci.2013.11.021. Epub 2014 Jan 7. No abstract available. Erratum in: J Allergy Clin Immunol. 2014 Aug;134(2):495.

PMID:
24406071
18.

Analysis of families with common variable immunodeficiency (CVID) and IgA deficiency suggests linkage of CVID to chromosome 16q.

Schäffer AA, Pfannstiel J, Webster AD, Plebani A, Hammarström L, Grimbacher B.

Hum Genet. 2006 Feb;118(6):725-9. Epub 2005 Nov 22.

19.

Common variable immunodeficiency: an update on etiology and management.

Yong PF, Tarzi M, Chua I, Grimbacher B, Chee R.

Immunol Allergy Clin North Am. 2008 May;28(2):367-86, ix-x. doi: 10.1016/j.iac.2008.01.001. Review.

PMID:
18424338
20.

Analysis of TACI mutations in CVID & RESPI patients who have inherited HLA B*44 or HLA*B8.

Waldrep ML, Zhuang Y, Schroeder HW Jr.

BMC Med Genet. 2009 Sep 23;10:100. doi: 10.1186/1471-2350-10-100.

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