PubMed (cited) for id: 177735

Year	Number of Results
1958	1
1959	1
1962	1
1978	1
1985	1
1991	1
1998	1
2000	1
2001	1
2003	1
2006	1
2007	1
2024	0

1

Mineralocorticoid receptor mutations are the principal cause of renal type 1 pseudohypoaldosteronism.

Pujo L, Fagart J, Gary F, Papadimitriou DT, Claës A, Jeunemaître X, Zennaro MC. Pujo L, et al. Hum Mutat. 2007 Jan;28(1):33-40. doi: 10.1002/humu.20371. Hum Mutat. 2007. PMID: 16972228

2

Elucidating the underlying molecular pathogenesis of NR3C2 mutants causing autosomal dominant pseudohypoaldosteronism type 1.

Riepe FG, Finkeldei J, de Sanctis L, Einaudi S, Testa A, Karges B, Peter M, Viemann M, Grötzinger J, Sippell WG, Fejes-Toth G, Krone N. Riepe FG, et al. J Clin Endocrinol Metab. 2006 Nov;91(11):4552-61. doi: 10.1210/jc.2006-1161. Epub 2006 Sep 5. J Clin Endocrinol Metab. 2006. PMID: 16954160

3

A salt-losing syndrome in infancy. Pseudo-hypoadrenocorticalism.

RAINE DN, ROY J. RAINE DN, et al. Arch Dis Child. 1962 Oct;37(195):548-56. doi: 10.1136/adc.37.195.548. Arch Dis Child. 1962. PMID: 13990509 Free PMC article. No abstract available.

4

Pseudohypo-adrenalocorticism; renal sodium loss, hyponatremia, and hyperkalemia due to a renal tubular insensitivity to mineralocorticoids.

DONNELL GN, LITMAN N, ROLDAN M. DONNELL GN, et al. AMA J Dis Child. 1959 Jun;97(6):813-28. AMA J Dis Child. 1959. PMID: 13649114 No abstract available.

5

A salt wasting syndrome in infancy.

CHEEK DB, PERRY JW. CHEEK DB, et al. Arch Dis Child. 1958 Jun;33(169):252-6. doi: 10.1136/adc.33.169.252. Arch Dis Child. 1958. PMID: 13545877 Free PMC article. No abstract available.

6

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. Sartorato P, et al. J Clin Endocrinol Metab. 2003 Jun;88(6):2508-17. doi: 10.1210/jc.2002-021932. J Clin Endocrinol Metab. 2003. PMID: 12788847

7

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. Viemann M, et al. J Clin Endocrinol Metab. 2001 May;86(5):2056-9. doi: 10.1210/jcem.86.5.7449. J Clin Endocrinol Metab. 2001. PMID: 11344206

8

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. Tajima T, et al. J Clin Endocrinol Metab. 2000 Dec;85(12):4690-4. doi: 10.1210/jcem.85.12.7078. J Clin Endocrinol Metab. 2000. PMID: 11134129

9

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. Geller DS, et al. Nat Genet. 1998 Jul;19(3):279-81. doi: 10.1038/966. Nat Genet. 1998. PMID: 9662404

10

Aldosterone-receptor deficiency in pseudohypoaldosteronism.

Armanini D, Kuhnle U, Strasser T, Dorr H, Butenandt I, Weber PC, Stockigt JR, Pearce P, Funder JW. Armanini D, et al. N Engl J Med. 1985 Nov 7;313(19):1178-81. doi: 10.1056/NEJM198511073131902. N Engl J Med. 1985. PMID: 2932642

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