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2. [Pseudohypoaldosteronism: familial forms. Eight case-reports, with a review of the literature (author's transl)]. Roy C; Cruveiller J; Harpey JP; Renault F; Debray P; Caille B Ann Pediatr (Paris); 1981 Oct; 28(8):553-8. PubMed ID: 7305233 [No Abstract] [Full Text] [Related]
4. [Pseudohypoaldosteronism: a special form of sodium loss in infancy]. Limbowo D; Monnens L; Wels C Tijdschr Kindergeneeskd; 1984 Oct; 52(5):200-4. PubMed ID: 6393425 [TBL] [Abstract][Full Text] [Related]
6. 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]
7. Pseudohypoaldosteronism in a female infant and her family: diversity of clinical expression and mode of inheritance. Chitayat D; Spirer Z; Ayalon D; Golander A Acta Paediatr Scand; 1985 Jul; 74(4):619-22. PubMed ID: 4024936 [TBL] [Abstract][Full Text] [Related]
8. [Autosomal recessive transmission of familial pseudohypoaldosteronism]. Bonnici F Arch Fr Pediatr; 1977 Nov; 34(9):915-6. PubMed ID: 606192 [No Abstract] [Full Text] [Related]
9. [Familial pseudohypoaldosteronism (apropos of 5 cases)]. Roy C Arch Fr Pediatr; 1977 Jan; 34(1):37-54. PubMed ID: 851368 [TBL] [Abstract][Full Text] [Related]
10. [Familial tubulopathy associating hypercalciuria and saline diabetes. Favorable results of indomethacin therapy]. Bétend B; Chopard P; Monier D; Guibaud P; Hermier M; Larbre F; François R Arch Fr Pediatr; 1979 Mar; 36(3):258-67. PubMed ID: 485770 [TBL] [Abstract][Full Text] [Related]
11. 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]
12. [A case of mineralocorticoid-resistant renal hyperkalemia without sodium wasting (type II pseudohypoaldosteronism)]. Ito K; Yamada K; Hasunuma K; Shiina T; Ebata T; Kikuno K; Yoshida S; Tamura Y; Yoshida S Nihon Naika Gakkai Zasshi; 1988 Mar; 77(3):425-9. PubMed ID: 3042897 [No Abstract] [Full Text] [Related]
14. Genetic heterogeneity of familial hypouricemia due to isolated renal tubular defect. Suzuki T; Kidoguchi K; Hayashi A Jinrui Idengaku Zasshi; 1981 Sep; 26(3):243-8. PubMed ID: 7334692 [No Abstract] [Full Text] [Related]
15. Pseudohypoaldosteronism: a review and report of two new cases. Speiser PW; Stoner E; New MI Adv Exp Med Biol; 1986; 196():173-95. PubMed ID: 3012977 [No Abstract] [Full Text] [Related]