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Items: 1 to 20 of 124

1.

HLA similarities indicate shared genetic risk in 21-hydroxylase autoantibody positive South African and United States Addison's disease.

Ross IL, Babu S, Armstrong T, Zhang L, Schatz D, Pugliese A, Eisenbarth G, Baker Ii P.

Tissue Antigens. 2014 Oct;84(4):361-9. doi: 10.1111/tan.12407. Epub 2014 Jul 18.

PMID:
25040682
2.

Dominant suppression of Addison's disease associated with HLA-B15.

Baker PR, Baschal EE, Fain PR, Nanduri P, Triolo TM, Siebert JC, Armstrong TK, Babu SR, Rewers MJ, Gottlieb PA, Barker JM, Eisenbarth GS.

J Clin Endocrinol Metab. 2011 Jul;96(7):2154-62. doi: 10.1210/jc.2010-2964. Epub 2011 May 11.

3.

Genetic determinants of 21-hydroxylase autoantibodies amongst patients of the Type 1 Diabetes Genetics Consortium.

Baker P, Fain P, Kahles H, Yu L, Hutton J, Wenzlau J, Rewers M, Badenhoop K, Eisenbarth G.

J Clin Endocrinol Metab. 2012 Aug;97(8):E1573-8. doi: 10.1210/jc.2011-2824. Epub 2012 Jun 20.

4.

Haplotype analysis discriminates genetic risk for DR3-associated endocrine autoimmunity and helps define extreme risk for Addison's disease.

Baker PR, Baschal EE, Fain PR, Triolo TM, Nanduri P, Siebert JC, Armstrong TK, Babu SR, Rewers MJ, Gottlieb PA, Barker JM, Eisenbarth GS.

J Clin Endocrinol Metab. 2010 Oct;95(10):E263-70. doi: 10.1210/jc.2010-0508. Epub 2010 Jul 14.

5.

Homozygosity of the polymorphism MICA5.1 identifies extreme risk of progression to overt adrenal insufficiency among 21-hydroxylase antibody-positive patients with type 1 diabetes.

Triolo TM, Baschal EE, Armstrong TK, Toews CS, Fain PR, Rewers MJ, Yu L, Miao D, Eisenbarth GS, Gottlieb PA, Barker JM.

J Clin Endocrinol Metab. 2009 Nov;94(11):4517-23. doi: 10.1210/jc.2009-1308. Epub 2009 Oct 9.

6.

Risk genes and autoantibodies in Egyptian children with type 1 diabetes - low frequency of autoantibodies in carriers of the HLA-DRB1*04:05-DQA1*03-DQB1*02 risk haplotype.

El-Amir MI, El-Feky MA, Laine AP, Härkönen T, El-Badawy O, Eltayeb AA, El-Melegy TT, Kiviniemi M, Knip M, Ilonen J.

Diabetes Metab Res Rev. 2015 Mar;31(3):287-94. doi: 10.1002/dmrr.2609. Epub 2014 Nov 24.

PMID:
25256132
7.

Autoimmune adrenocortical failure in Norway autoantibodies and human leukocyte antigen class II associations related to clinical features.

Myhre AG, Undlien DE, Løvås K, Uhlving S, Nedrebø BG, Fougner KJ, Trovik T, Sørheim JI, Husebye ES.

J Clin Endocrinol Metab. 2002 Feb;87(2):618-23.

PMID:
11836294
9.

Microsatellite polymorphism of the MHC class I chain-related (MIC-A and MIC-B) genes marks the risk for autoimmune Addison's disease.

Gambelunghe G, Falorni A, Ghaderi M, Laureti S, Tortoioli C, Santeusanio F, Brunetti P, Sanjeevi CB.

J Clin Endocrinol Metab. 1999 Oct;84(10):3701-7.

PMID:
10523017
10.

Analysis of extended human leukocyte antigen haplotype association with Addison's disease in three populations.

Gombos Z, Hermann R, Kiviniemi M, Nejentsev S, Reimand K, Fadeyev V, Peterson P, Uibo R, Ilonen J.

Eur J Endocrinol. 2007 Dec;157(6):757-61.

PMID:
18057383
11.

The association of specific HLA class I and II alleles with type 1 diabetes among Filipinos.

Bugawan TL, Klitz W, Alejandrino M, Ching J, Panelo A, Solfelix CM, Petrone A, Buzzetti R, Pozzilli P, Erlich HA.

Tissue Antigens. 2002 Jun;59(6):452-69.

PMID:
12445315
12.

HLA class II haplotypes differentiate between the adult autoimmune polyglandular syndrome types II and III.

Flesch BK, Matheis N, Alt T, Weinstock C, Bux J, Kahaly GJ.

J Clin Endocrinol Metab. 2014 Jan;99(1):E177-82. doi: 10.1210/jc.2013-2852. Epub 2013 Dec 20.

PMID:
24187405
13.

Predicting the onset of Addison's disease: ACTH, renin, cortisol and 21-hydroxylase autoantibodies.

Baker PR, Nanduri P, Gottlieb PA, Yu L, Klingensmith GJ, Eisenbarth GS, Barker JM.

Clin Endocrinol (Oxf). 2012 May;76(5):617-24. doi: 10.1111/j.1365-2265.2011.04276.x.

15.

T cell responses to steroid cytochrome P450 21-hydroxylase in patients with autoimmune primary adrenal insufficiency.

Bratland E, Skinningsrud B, Undlien DE, Mozes E, Husebye ES.

J Clin Endocrinol Metab. 2009 Dec;94(12):5117-24. doi: 10.1210/jc.2009-1115. Epub 2009 Nov 4.

PMID:
19890026
16.

Additional association of intra-MHC genes, MICA and D6S273, with Addison's disease.

Park YS, Sanjeevi CB, Robles D, Yu L, Rewers M, Gottlieb PA, Fain P, Eisenbarth GS.

Tissue Antigens. 2002 Aug;60(2):155-63.

PMID:
12392510
17.

Susceptibility and resistance alleles of human leukocyte antigen (HLA) DQA1 and HLA DQB1 are shared in endocrine autoimmune disease.

Badenhoop K, Walfish PG, Rau H, Fischer S, Nicolay A, Bogner U, Schleusener H, Usadel KH.

J Clin Endocrinol Metab. 1995 Jul;80(7):2112-7.

PMID:
7608264
18.

DRB1*04 and DQ alleles: expression of 21-hydroxylase autoantibodies and risk of progression to Addison's disease.

Yu L, Brewer KW, Gates S, Wu A, Wang T, Babu SR, Gottlieb PA, Freed BM, Noble J, Erlich HA, Rewers MJ, Eisenbarth GS.

J Clin Endocrinol Metab. 1999 Jan;84(1):328-35.

PMID:
9920103
19.

HLA class II genotyping of African American type 1 diabetic patients reveals associations unique to African haplotypes.

Noble JA, Johnson J, Lane JA, Valdes AM.

Diabetes. 2013 Sep;62(9):3292-9. doi: 10.2337/db13-0094. Epub 2013 Jun 25.

20.

21-Hydroxylase epitopes are targeted by CD8 T cells in autoimmune Addison's disease.

Rottembourg D, Deal C, Lambert M, Mallone R, Carel JC, Lacroix A, Caillat-Zucman S, le Deist F.

J Autoimmun. 2010 Dec;35(4):309-15. doi: 10.1016/j.jaut.2010.07.001. Epub 2010 Aug 3.

PMID:
20685079

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