Gordon RD - Search Results

1

Further evidence for linkage of familial hyperaldosteronism type II at chromosome 7p22 in Italian as well as Australian and South American families.

Sukor N, Mulatero P, Gordon RD, So A, Duffy D, Bertello C, Kelemen L, Jeske Y, Veglio F, Stowasser M. Sukor N, et al. Among authors: gordon rd. J Hypertens. 2008 Aug;26(8):1577-82. doi: 10.1097/HJH.0b013e3283028352. J Hypertens. 2008. PMID: 18622235

2

Genomic structure of the human gene for protein kinase A regulatory subunit R1-beta (PRKAR1B) on 7p22: no evidence for mutations in familial hyperaldosteronism type II in a large affected kindred.

Elphinstone MS, Gordon RD, So A, Jeske YW, Stratakis CA, Stowasser M. Elphinstone MS, et al. Among authors: gordon rd. Clin Endocrinol (Oxf). 2004 Dec;61(6):716-23. doi: 10.1111/j.1365-2265.2004.02155.x. Clin Endocrinol (Oxf). 2004. PMID: 15579186

3

Familial hyperaldosteronism type II is linked to the chromosome 7p22 region but also shows predicted heterogeneity.

So A, Duffy DL, Gordon RD, Jeske YW, Lin-Su K, New MI, Stowasser M. So A, et al. Among authors: gordon rd. J Hypertens. 2005 Aug;23(8):1477-84. doi: 10.1097/01.hjh.0000174299.66369.26. J Hypertens. 2005. PMID: 16003173

4

Clinical, biochemical and genetic approaches to the detection of familial hyperaldosteronism type I.

Stowasser M, Bachmann AW, Jonsson JR, Tunny TJ, Klemm SA, Gordon RD. Stowasser M, et al. Among authors: gordon rd. J Hypertens. 1995 Dec;13(12 Pt 2):1610-3. J Hypertens. 1995. PMID: 8903619

5

Evidence for persistent dysfunction of wild-type aldosterone synthase gene in glucocorticoid-treated familial hyperaldosteronism type I.

Stowasser M, Taylor WL, Gartside MG, Tunny TJ, Gordon RD. Stowasser M, et al. Among authors: gordon rd. J Hypertens. 1997 Dec;15(12 Pt 2):1729-33. doi: 10.1097/00004872-199715120-00080. J Hypertens. 1997. PMID: 9488230

6

Primary aldosteronism: learning from the study of familial varieties.

Stowasser M, Gordon RD. Stowasser M, et al. Among authors: gordon rd. J Hypertens. 2000 Sep;18(9):1165-76. doi: 10.1097/00004872-200018090-00002. J Hypertens. 2000. PMID: 10994747 Review.

7

Familial hyperaldosteronism.

Stowasser M, Gordon RD. Stowasser M, et al. Among authors: gordon rd. J Steroid Biochem Mol Biol. 2001 Sep;78(3):215-29. doi: 10.1016/s0960-0760(01)00097-8. J Steroid Biochem Mol Biol. 2001. PMID: 11595502 Review.

8

Examination of chromosome 7p22 candidate genes RBaK, PMS2 and GNA12 in familial hyperaldosteronism type II.

Jeske YW, So A, Kelemen L, Sukor N, Willys C, Bulmer B, Gordon RD, Duffy D, Stowasser M. Jeske YW, et al. Among authors: gordon rd. Clin Exp Pharmacol Physiol. 2008 Apr;35(4):380-5. doi: 10.1111/j.1440-1681.2008.04882.x. Clin Exp Pharmacol Physiol. 2008. PMID: 18307725

9

The renaissance of primary aldosteronism: what has it taught us?

Stowasser M, Gordon RD. Stowasser M, et al. Among authors: gordon rd. Heart Lung Circ. 2013 Jun;22(6):412-20. doi: 10.1016/j.hlc.2013.01.006. Epub 2013 Feb 9. Heart Lung Circ. 2013. PMID: 23402683 Review.

10

Primary aldosteronism: from genesis to genetics.

Stowasser M, Gordon RD. Stowasser M, et al. Among authors: gordon rd. Trends Endocrinol Metab. 2003 Sep;14(7):310-7. doi: 10.1016/s1043-2760(03)00112-7. Trends Endocrinol Metab. 2003. PMID: 12946873 Review. No abstract available.

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