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Journal Abstract Search

183 related items for PubMed ID: 26817011

  • 1. Pseudohypoaldosteronism in a newborn male with functional polymorphisms in the mineralocorticoid receptor genes.
    Jeong HA, Park YK, Jung YS, Nam MH, Nam HK, Lee KH, Rhie YJ.
    Ann Pediatr Endocrinol Metab; 2015 Dec; 20(4):230-4. PubMed ID: 26817011
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  • 2. A case of pseudohypoaldosteronism type 1 with a mutation in the mineralocorticoid receptor gene.
    Lee SE, Jung YH, Han KH, Lee HK, Kang HG, Ha IS, Choi Y, Cheong HI.
    Korean J Pediatr; 2011 Feb; 54(2):90-3. PubMed ID: 21503203
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  • 3. A Neonate with Autosomal Dominant Pseudohypoaldosteronism Type 1 Due to a Novel Microdeletion of the NR3C2 Gene at 4q31.23.
    Kim SJ, Park D, Jang W, Lee J.
    Children (Basel); 2021 Nov 25; 8(12):. PubMed ID: 34943285
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  • 4. Clinical and molecular features of type 1 pseudohypoaldosteronism.
    Riepe FG.
    Horm Res; 2009 Nov 25; 72(1):1-9. PubMed ID: 19571553
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  • 7. Novel mutations in the SCNN1A gene causing Pseudohypoaldosteronism type 1.
    Wang J, Yu T, Yin L, Li J, Yu L, Shen Y, Yu Y, Shen Y, Fu Q.
    PLoS One; 2013 Nov 25; 8(6):e65676. PubMed ID: 23762408
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  • 13. Exclusion of serum- and glucocorticoid-induced kinase 1 (SGK1) as a candidate gene for genetically heterogeneous renal pseudohypoaldosteronism type I in eight families.
    Riepe FG, Holterhus PM.
    Am J Nephrol; 2007 Nov 25; 27(2):164-9. PubMed ID: 17317952
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  • 17. 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 25; 89(1):227-31. PubMed ID: 14715854
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  • 18. Systemic Pseudohypoaldosteronism Type 1 due to 3 Novel Mutations in SCNN1Aand SCNN1BGenes.
    Cayir A, Demirelli Y, Yildiz D, Kahveci H, Yarali O, Kurnaz E, Vuralli D, Demirbilek H.
    Horm Res Paediatr; 2019 Jan 25; 91(3):175-185. PubMed ID: 31018202
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  • 19. Two Japanese patients with the renal form of pseudohypoaldosteronism type 1 caused by mutations of NR3C2.
    Morikawa S, Komatsu N, Sakata S, Nakamura-Utsunomiya A, Okada S, Tajima T.
    Clin Pediatr Endocrinol; 2015 Jul 25; 24(3):135-8. PubMed ID: 26594094
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