163 related articles for article (PubMed ID: 1659876)
1. 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]
2. 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]
3. 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]
4. 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]
5. 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]
6. 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]
7. 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]
8. Generalized unresponsiveness to mineralocorticoid hormones: familial recessive pseudohypoaldosteronism due to aldosterone-receptor deficiency.
Bosson D; Kuhnle U; Mees N; Ramet J; Vamos E; Vertongen F; Wolter R; Armanini D
Acta Endocrinol Suppl (Copenh); 1986; 279():376-80. PubMed ID: 2946135
[TBL] [Abstract][Full Text] [Related]
9. 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]
10. [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]
11. A novel nonsense mutation of the mineralocorticoid receptor gene in the renal form of pseudohypoaldosteronism type 1.
Uchida N; Shiohara M; Miyagawa S; Yokota I; Mori T
J Pediatr Endocrinol Metab; 2009 Jan; 22(1):91-5. PubMed ID: 19344080
[TBL] [Abstract][Full Text] [Related]
12. Mineralocorticoid resistance.
Zennaro MC; Lombès M
Trends Endocrinol Metab; 2004 Aug; 15(6):264-70. PubMed ID: 15358279
[TBL] [Abstract][Full Text] [Related]
13. [Receptor-effector relations in the effect of adosterone on mononuclear leukocytes: validation and application to various water and electrolyte imbalances in humans].
Wehling M
Klin Wochenschr; 1989 Jan; 67(1):1-5. PubMed ID: 2537910
[TBL] [Abstract][Full Text] [Related]
14. 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]
15. The determination of mineralocorticoid receptors in human mononuclear leukocytes from patients with mineralocorticoid excess: physiological and pathological implications.
Armanini D; Kuhnle U; Witzgall H; Tietze U; Saule H; Schroeter C; Strasser T; Butenandt I; Bidlingmaier F; Weber PC
Clin Exp Hypertens A; 1986; 8(4-5):781-5. PubMed ID: 3019593
[TBL] [Abstract][Full Text] [Related]
16. Exclusion of the locus for autosomal recessive pseudohypoaldosteronism type 1 from the mineralocorticoid receptor gene region on human chromosome 4q by linkage analysis.
Chung E; Hanukoglu A; Rees M; Thompson R; Dillon M; Hanukoglu I; Bistritzer T; Kuhnle U; Seckl J; Gardiner RM
J Clin Endocrinol Metab; 1995 Nov; 80(11):3341-5. PubMed ID: 7593448
[TBL] [Abstract][Full Text] [Related]
17. 30 YEARS OF THE MINERALOCORTICOID RECEPTOR: Mineralocorticoid receptor mutations.
Zennaro MC; Fernandes-Rosa F
J Endocrinol; 2017 Jul; 234(1):T93-T106. PubMed ID: 28348114
[TBL] [Abstract][Full Text] [Related]
18. 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]
19. 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]
20. No alteration in the primary structure of the mineralocorticoid receptor in a family with pseudohypoaldosteronism.
Zennaro MC; Borensztein P; Jeunemaitre X; Armanini D; Soubrier F
J Clin Endocrinol Metab; 1994 Jul; 79(1):32-8. PubMed ID: 8027248
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]