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Items: 1 to 20 of 166

1.

Familial varieties of primary aldosteronism.

Stowasser M, Gunasekera TG, Gordon RD.

Clin Exp Pharmacol Physiol. 2001 Dec;28(12):1087-90. Review.

PMID:
11903322
2.

Primary aldosteronism: learning from the study of familial varieties.

Stowasser M, Gordon RD.

J Hypertens. 2000 Sep;18(9):1165-76. Review.

PMID:
10994747
3.

Familial hyperaldosteronism.

Stowasser M, Gordon RD.

J Steroid Biochem Mol Biol. 2001 Sep;78(3):215-29. Review.

PMID:
11595502
4.

New genetic insights in familial hyperaldosteronism.

Jackson RV, Lafferty A, Torpy DJ, Stratakis C.

Ann N Y Acad Sci. 2002 Sep;970:77-88. Review.

PMID:
12381543
5.

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.

J Hypertens. 2005 Aug;23(8):1477-84.

PMID:
16003173
6.

[Familial hyperaldosteronism].

Spoto B, Furlò G, Gervasi A, Bresolin G, Zoccali C.

G Ital Nefrol. 2004 Mar-Apr;21(2):139-43. Review. Italian.

PMID:
15351948
7.

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.

J Hypertens. 2008 Aug;26(8):1577-82. doi: 10.1097/HJH.0b013e3283028352.

PMID:
18622235
8.

Familial hyperaldosteronism type II: description of a large kindred and exclusion of the aldosterone synthase (CYP11B2) gene.

Torpy DJ, Gordon RD, Lin JP, Huggard PR, Taymans SE, Stowasser M, Chrousos GP, Stratakis CA.

J Clin Endocrinol Metab. 1998 Sep;83(9):3214-8.

PMID:
9745430
9.

Familial hyperaldosteronism.

Torpy DJ, Stratakis CA, Chrousos GP.

Braz J Med Biol Res. 2000 Oct;33(10):1149-55. Review.

10.
11.

A novel genetic locus for low renin hypertension: familial hyperaldosteronism type II maps to chromosome 7 (7p22).

Lafferty AR, Torpy DJ, Stowasser M, Taymans SE, Lin JP, Huggard P, Gordon RD, Stratakis CA.

J Med Genet. 2000 Nov;37(11):831-5.

12.

Familial hyperaldosteronism type II: five families with a new variety of primary aldosteronism.

Stowasser M, Gordon RD, Tunny TJ, Klemm SA, Finn WL, Krek AL.

Clin Exp Pharmacol Physiol. 1992 May;19(5):319-22.

PMID:
1521363
13.

Genetic screening for glucocorticoid-remediable aldosteronism (GRA): experience of three clinical centres in Poland.

Adler G, Widecka K, Peczkowska M, Dobrucki T, Placha G, Drozd R, Parczewski M, Januszewicz A, Gaciong Z, Ciechanowicz A.

J Appl Genet. 2005;46(3):329-32.

PMID:
16110193
14.

Primary aldosteronism.

Gordon RD.

J Endocrinol Invest. 1995 Jul-Aug;18(7):495-511. Review.

PMID:
9221268
15.

A chimeric CYP11B1/CYP11B2 gene in glucocorticoid-insuppressible familial hyperaldosteronism.

Ise T, Shimoda A, Takakuwa H, Kato T, Izumiya Y, Shimizu K, Suzuki T, Sasano H, Yokoyama H, Kobayashi K.

Clin Endocrinol (Oxf). 2001 Jul;55(1):131-4.

PMID:
11453962
16.

SFE/SFHTA/AFCE consensus on primary aldosteronism, part 5: Genetic diagnosis of primary aldosteronism.

Zennaro MC, Jeunemaitre X.

Ann Endocrinol (Paris). 2016 Jul;77(3):214-9. doi: 10.1016/j.ando.2016.02.006. Epub 2016 Jun 15.

PMID:
27315758
17.

Genetic alterations in patients with primary aldosteronism.

Takeda Y.

Hypertens Res. 2001 Sep;24(5):469-74. Review.

18.

Genetics of primary aldosteronism.

Mulatero P, Morello F, Veglio F.

J Hypertens. 2004 Apr;22(4):663-70. Review.

PMID:
15126900
19.

Genetics of primary aldosteronism.

Gordon RD, Klemm SA, Tunny TJ, Stowasser M.

Clin Exp Pharmacol Physiol. 1994 Nov;21(11):915-8.

PMID:
7882585
20.

Mutation analysis of CYP11B1 and CYP11B2 in patients with increased 18-hydroxycortisol production.

Nicod J, Dick B, Frey FJ, Ferrari P.

Mol Cell Endocrinol. 2004 Feb 12;214(1-2):167-74.

PMID:
15062555

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