Similar articles for PMID: 21795453

Year	Number of Results
1978	1
1986	1
1988	1
1989	1
1990	2
1991	2
1992	1
1994	4
1995	3
1996	4
1997	1
1998	2
1999	2
2000	1
2001	2
2002	1
2003	5
2004	3
2005	4
2006	4
2007	5
2008	1
2009	4
2010	8
2011	5
2012	5
2013	1
2014	5
2015	7
2016	8
2017	2
2018	4
2019	2
2021	3
2022	1
2024	0

1

Clinical manifestations of highly prevalent corticosteroid-binding globulin mutations in a village in southern Italy.

Cizza G, Bernardi L, Smirne N, Maletta R, Tomaino C, Costanzo A, Gallo M, Lewis JG, Geracitano S, Grasso MB, Potenza G, Monteleone C, Brancati G, Ho JT, Torpy DJ, Bruni AC. Cizza G, et al. J Clin Endocrinol Metab. 2011 Oct;96(10):E1684-93. doi: 10.1210/jc.2011-1321. Epub 2011 Jul 27. J Clin Endocrinol Metab. 2011. PMID: 21795453 Free PMC article.

2

Familial corticosteroid-binding globulin deficiency due to a novel null mutation: association with fatigue and relative hypotension.

Torpy DJ, Bachmann AW, Grice JE, Fitzgerald SP, Phillips PJ, Whitworth JA, Jackson RV. Torpy DJ, et al. J Clin Endocrinol Metab. 2001 Aug;86(8):3692-700. doi: 10.1210/jcem.86.8.7724. J Clin Endocrinol Metab. 2001. PMID: 11502797

3

Hereditary corticosteroid-binding globulin deficiency due to a missense mutation (Asp367Asn, CBG Lyon) in a Brazilian kindred.

Brunner E, Baima J, Vieira TC, Vieira JG, Abucham J. Brunner E, et al. Clin Endocrinol (Oxf). 2003 Jun;58(6):756-62. doi: 10.1046/j.1365-2265.2003.01783.x. Clin Endocrinol (Oxf). 2003. PMID: 12780753

4

Corticosteroid-binding globulin: the clinical significance of altered levels and heritable mutations.

Gagliardi L, Ho JT, Torpy DJ. Gagliardi L, et al. Mol Cell Endocrinol. 2010 Mar 5;316(1):24-34. doi: 10.1016/j.mce.2009.07.015. Epub 2009 Jul 28. Mol Cell Endocrinol. 2010. PMID: 19643166 Review.

5

Corticosteroid-binding globulin gene polymorphisms: clinical implications and links to idiopathic chronic fatigue disorders.

Torpy DJ, Ho JT. Torpy DJ, et al. Clin Endocrinol (Oxf). 2007 Aug;67(2):161-7. doi: 10.1111/j.1365-2265.2007.02890.x. Epub 2007 Jun 4. Clin Endocrinol (Oxf). 2007. PMID: 17547679 Review.

6

CBG Santiago: a novel CBG mutation.

Torpy DJ, Lundgren BA, Ho JT, Lewis JG, Scott HS, Mericq V. Torpy DJ, et al. J Clin Endocrinol Metab. 2012 Jan;97(1):E151-5. doi: 10.1210/jc.2011-2022. Epub 2011 Oct 19. J Clin Endocrinol Metab. 2012. PMID: 22013108

7

Effect of mutations of the human serpin protein corticosteroid-binding globulin on cortisol-binding, thermal and protease sensitivity.

Braun BC, Meyer HA, Reetz A, Fuhrmann U, Köhrle J. Braun BC, et al. J Steroid Biochem Mol Biol. 2010 May;120(1):30-7. doi: 10.1016/j.jsbmb.2010.03.014. Epub 2010 Mar 11. J Steroid Biochem Mol Biol. 2010. PMID: 20226861

8

Two different corticosteroid-binding globulin variants that lack cortisol-binding activity in a greek woman.

Hill LA, Vassiliadi DA, Simard M, Pavlaki A, Perogamvros I, Hadjidakis D, Hammond GL. Hill LA, et al. J Clin Endocrinol Metab. 2012 Nov;97(11):4260-7. doi: 10.1210/jc.2012-2467. Epub 2012 Sep 4. J Clin Endocrinol Metab. 2012. PMID: 22948765

9

Novel human corticosteroid-binding globulin variant with low cortisol-binding affinity.

Emptoz-Bonneton A, Cousin P, Seguchi K, Avvakumov GV, Bully C, Hammond GL, Pugeat M. Emptoz-Bonneton A, et al. J Clin Endocrinol Metab. 2000 Jan;85(1):361-7. doi: 10.1210/jcem.85.1.6315. J Clin Endocrinol Metab. 2000. PMID: 10634411

10

Association between chronic fatigue syndrome and the corticosteroid-binding globulin gene ALA SER224 polymorphism.

Torpy DJ, Bachmann AW, Gartside M, Grice JE, Harris JM, Clifton P, Easteal S, Jackson RV, Whitworth JA. Torpy DJ, et al. Endocr Res. 2004 Aug;30(3):417-29. doi: 10.1081/erc-200035599. Endocr Res. 2004. PMID: 15554358 Clinical Trial.

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