157 related articles for article (PubMed ID: 7792804)
1. Familial pseudohypoaldosteronism: a review on the heterogeneity of the syndrome.
Kuhnle U; Hinkel GK; Akkurt HI; Krozowski Z
Steroids; 1995 Jan; 60(1):157-60. PubMed ID: 7792804
[TBL] [Abstract][Full Text] [Related]
2. Pseudohypoaldosteronism: family studies to identify asymptomatic carriers by stimulation of the renin-aldosterone system.
Kuhnle U; Hinkel GK; Hubl W; Reichelt T
Horm Res; 1996; 46(3):124-9. PubMed ID: 8894667
[TBL] [Abstract][Full Text] [Related]
3. Immunofluorescence of mineralocorticoid receptors in peripheral lymphocytes: presence of receptor-like activity in patients with the autosomal dominant form of pseudohypoaldosteronism, and its absence in the recessive form.
Kuhnle U; Keller U; Armanini D; Funder J; Krozowski Z
J Steroid Biochem Mol Biol; 1994 Dec; 51(5-6):267-73. PubMed ID: 7826888
[TBL] [Abstract][Full Text] [Related]
4. Mineralocorticoid resistance.
Zennaro MC; Lombès M
Trends Endocrinol Metab; 2004 Aug; 15(6):264-70. PubMed ID: 15358279
[TBL] [Abstract][Full Text] [Related]
5. Pseudohypoaldosteronism in eight families: different forms of inheritance are evidence for various genetic defects.
Kuhnle U; Nielsen MD; Tietze HU; Schroeter CH; Schlamp D; Bosson D; Knorr D; Armanini D
J Clin Endocrinol Metab; 1990 Mar; 70(3):638-41. PubMed ID: 2137831
[TBL] [Abstract][Full Text] [Related]
6. Pseudohypoaldosteronism and mineralocorticoid receptor abnormalities.
Armanini D; Wehling M; Da Dalt L; Zennaro M; Scali U; Keller U; Pratesi C; Mantero F; Kuhnle U
J Steroid Biochem Mol Biol; 1991; 40(1-3):363-5. PubMed ID: 1659876
[TBL] [Abstract][Full Text] [Related]
7. Inactivating mutations of the mineralocorticoid receptor in Type I pseudohypoaldosteronism.
Sartorato P; Khaldi Y; Lapeyraque AL; Armanini D; Kuhnle U; Salomon R; Caprio M; Viengchareun S; Lombès M; Zennaro MC
Mol Cell Endocrinol; 2004 Mar; 217(1-2):119-25. PubMed ID: 15134810
[TBL] [Abstract][Full Text] [Related]
8. [Mineralocorticoid resistance: pseudohypoaldosteronism type 1].
Fernandes-Rosa FL; Antonini SR
Arq Bras Endocrinol Metabol; 2007 Apr; 51(3):373-81. PubMed ID: 17546235
[TBL] [Abstract][Full Text] [Related]
9. Evidence for genetic heterogeneity of pseudohypoaldosteronism type 1: identification of a novel mutation in the human mineralocorticoid receptor in one sporadic case and no mutations in two autosomal dominant kindreds.
Viemann M; Peter M; López-Siguero JP; Simic-Schleicher G; Sippell WG
J Clin Endocrinol Metab; 2001 May; 86(5):2056-9. PubMed ID: 11344206
[TBL] [Abstract][Full Text] [Related]
10. Clinical and molecular analysis of six Japanese patients with a renal form of pseudohypoaldosteronism type 1.
Hatta Y; Nakamura A; Hara S; Kamijo T; Iwata J; Hamajima T; Abe M; Okada M; Ushio M; Tsuyuki K; Tajima T
Endocr J; 2013; 60(3):299-304. PubMed ID: 23197115
[TBL] [Abstract][Full Text] [Related]
11. A novel missense mutation of mineralocorticoid receptor gene in one Japanese family with a renal form of pseudohypoaldosteronism type 1.
Tajima T; Kitagawa H; Yokoya S; Tachibana K; Adachi M; Nakae J; Suwa S; Katoh S; Fujieda K
J Clin Endocrinol Metab; 2000 Dec; 85(12):4690-4. PubMed ID: 11134129
[TBL] [Abstract][Full Text] [Related]
12. Mutations in the mineralocorticoid receptor gene cause autosomal dominant pseudohypoaldosteronism type I.
Geller DS; Rodriguez-Soriano J; Vallo Boado A; Schifter S; Bayer M; Chang SS; Lifton RP
Nat Genet; 1998 Jul; 19(3):279-81. PubMed ID: 9662404
[TBL] [Abstract][Full Text] [Related]
13. A novel nonsense mutation of the mineralocorticoid receptor gene in a Swedish family with pseudohypoaldosteronism type I (PHA1).
Nyström AM; Bondeson ML; Skanke N; Mårtensson J; Strömberg B; Gustafsson J; Annerén G
J Clin Endocrinol Metab; 2004 Jan; 89(1):227-31. PubMed ID: 14715854
[TBL] [Abstract][Full Text] [Related]
14. Polymorphisms of amiloride-sensitive sodium channel subunits in five sporadic cases of pseudohypoaldosteronism: do they have pathologic potential?
Arai K; Zachman K; Shibasaki T; Chrousos GP
J Clin Endocrinol Metab; 1999 Jul; 84(7):2434-7. PubMed ID: 10404817
[TBL] [Abstract][Full Text] [Related]
15. Inheritance of mineralocorticoid effector abnormalities of human mononuclear leucocytes in families with pseudohypoaldosteronism.
Wehling M; Kuhnle U; Daumer C; Armanini D
Clin Endocrinol (Oxf); 1989 Nov; 31(5):597-605. PubMed ID: 2627754
[TBL] [Abstract][Full Text] [Related]
16. Cardiovascular effects of aldosterone: insight from adult carriers of mineralocorticoid receptor mutations.
Escoubet B; Couffignal C; Laisy JP; Mangin L; Chillon S; Laouénan C; Serfaty JM; Jeunemaitre X; Mentré F; Zennaro MC
Circ Cardiovasc Genet; 2013 Aug; 6(4):381-90. PubMed ID: 23852419
[TBL] [Abstract][Full Text] [Related]
17. Renin-aldosterone system evaluation over four decades in an extended family with autosomal dominant pseudohypoaldosteronism due to a deletion in the NR3C2 gene.
Hanukoglu A; Vargas-Poussou R; Landau Z; Yosovich K; Hureaux M; Zennaro MC
J Steroid Biochem Mol Biol; 2020 Nov; 204():105755. PubMed ID: 33017655
[TBL] [Abstract][Full Text] [Related]
18. Molecular pathogenesis of renal pseudohypoaldosteronism type 1.
Riepe FG
Expert Rev Endocrinol Metab; 2007 May; 2(3):407-419. PubMed ID: 30743803
[TBL] [Abstract][Full Text] [Related]
19. Different inactivating mutations of the mineralocorticoid receptor in fourteen families affected by type I pseudohypoaldosteronism.
Sartorato P; Lapeyraque AL; Armanini D; Kuhnle U; Khaldi Y; Salomon R; Abadie V; Di Battista E; Naselli A; Racine A; Bosio M; Caprio M; Poulet-Young V; Chabrolle JP; Niaudet P; De Gennes C; Lecornec MH; Poisson E; Fusco AM; Loli P; Lombès M; Zennaro MC
J Clin Endocrinol Metab; 2003 Jun; 88(6):2508-17. PubMed ID: 12788847
[TBL] [Abstract][Full Text] [Related]
20. Recurrence of the R947X mutation in unrelated families with autosomal dominant pseudohypoaldosteronism type 1: evidence for a mutational hot spot in the mineralocorticoid receptor gene.
Fernandes-Rosa FL; de Castro M; Latronico AC; Sippell WG; Riepe FG; Antonini SR
J Clin Endocrinol Metab; 2006 Sep; 91(9):3671-5. PubMed ID: 16757525
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
