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Journal Abstract Search

154 related items for PubMed ID: 31529157

  • 41. Familial cases of pseudohypoaldosteronism type II harboring a novel mutation in the Cullin 3 gene.
    Nakano K, Kubota Y, Mori T, Chiga M, Mori T, Sonoda S, Ueda D, Asakura I, Ikegaya T, Kagawa J, Uchida S, Kubota A.
    Nephrology (Carlton); 2020 Nov; 25(11):818-821. PubMed ID: 32619053
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  • 42. A mouse model of pseudohypoaldosteronism type II reveals a novel mechanism of renal tubular acidosis.
    López-Cayuqueo KI, Chavez-Canales M, Pillot A, Houillier P, Jayat M, Baraka-Vidot J, Trepiccione F, Baudrie V, Büsst C, Soukaseum C, Kumai Y, Jeunemaître X, Hadchouel J, Eladari D, Chambrey R.
    Kidney Int; 2018 Sep; 94(3):514-523. PubMed ID: 30146013
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  • 43. [Arterial hypertension with hyperkalemia, tubular acidosis and normal renal function: Gordon syndrome and/or pseudohypoaldosteronism type II?].
    Ader JL, Waeber B, Suc JM, Brunner HR, Tran-Van T, Durand D, Praddaude F.
    Arch Mal Coeur Vaiss; 1988 Jun; 81 Spec No():193-7. PubMed ID: 2973296
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  • 44. Elevated plasma asymmetric dimethyl-L-arginine in a patient with Gordon syndrome.
    Wieczorek-Surdacka E, Surdacki A, Bode-Böger SM, Schubert B, Sulowicz W.
    Nephrol Dial Transplant; 2007 Jan; 22(1):268-71. PubMed ID: 16998213
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  • 45. A rare cause of hypertension in childhood: Answers.
    Kucuk N, Yavas Abalı Z, Abalı S, Canpolat N, Yesil G, Turan S, Bereket A, Guran T.
    Pediatr Nephrol; 2020 Jan; 35(1):79-82. PubMed ID: 31541304
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  • 48. 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
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  • 52. A family with liddle's syndrome caused by a mutation in the beta subunit of the epithelial sodium channel.
    Kyuma M, Ura N, Torii T, Takeuchi H, Takizawa H, Kitamura K, Tomita K, Sasaki S, Shimamoto K.
    Clin Exp Hypertens; 2001 Aug; 23(6):471-8. PubMed ID: 11478429
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  • 54. A novel mutation of the epithelial Na+ channel causes type 1 pseudohypoaldosteronism.
    Bonny O, Knoers N, Monnens L, Rossier BC.
    Pediatr Nephrol; 2002 Oct; 17(10):804-8. PubMed ID: 12376807
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  • 57. 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 31; 217(1-2):119-25. PubMed ID: 15134810
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  • 58. Pseudohypoaldosteronism: mineralocorticoid unresponsiveness syndrome.
    Jaruratanasirikul S, Janjindamai W.
    J Med Assoc Thai; 2000 Aug 31; 83(8):948-52. PubMed ID: 10998851
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  • 59. Pseudohypoaldosteronism Type II Caused by CUL3 Mutation Presented with Visual Impairment.
    Wang Q, Cao BY, Su C, Li WJ, Gong CX.
    Chin Med J (Engl); 2018 Aug 05; 131(15):1879-1881. PubMed ID: 30058590
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  • 60. Plasma aldosterone in essential hypertension with low renin activity.
    Fukuchi S, Nakajima K, Takenouchi T, Nishisato K.
    Jpn Circ J; 1974 Dec 05; 38(12):1071-7. PubMed ID: 4436936
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