These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

284 related articles for article (PubMed ID: 20431271)

  • 1. Hook effect: a pitfall leading to misdiagnosis of hypoaldosteronism in an infant with pseudohypoaldosteronism.
    Akin L; Kurtoglu S; Kendirci M; Akin MA; Hartmann MF; Wudy SA
    Horm Res Paediatr; 2010; 74(1):72-5. PubMed ID: 20431271
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Aldosterone deficiency with a hormone profile mimicking pseudohypoaldosteronism.
    Martín-Rivada Á; Argente J; Martos-Moreno GÁ
    J Pediatr Endocrinol Metab; 2020 Nov; 33(11):1501-1505. PubMed ID: 32809961
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Multisteroid analysis in children with terminal aldosterone biosynthesis defects.
    Peter M; Partsch CJ; Sippell WG
    J Clin Endocrinol Metab; 1995 May; 80(5):1622-7. PubMed ID: 7745009
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Reduced Na+, K(+)-ATPase activity in patients with pseudohypoaldosteronism.
    Bistritzer T; Evans S; Cotariu D; Goldberg M; Aladjem M
    Pediatr Res; 1994 Mar; 35(3):372-5. PubMed ID: 8190530
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Diagnostic value of plasma aldosterone/potassium ratio in hypoaldosteronism.
    Shiah CJ; Wu KD; Tsai DM; Liao ST; Siauw CP; Lee LS
    J Formos Med Assoc; 1995 May; 94(5):248-54. PubMed ID: 7613258
    [TBL] [Abstract][Full Text] [Related]  

  • 6. [Primary hypoaldosteronism, pseudo-hypoaldosteronism and distal tubular acidosis].
    Klaus D
    Klin Wochenschr; 1984 Aug; 62(16):747-52. PubMed ID: 6384650
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Corticosterone Methyl Oxidase Deficiency Type 1 with Normokalemia in an Infant.
    Üstyol A; Atabek ME; Taylor N; Yeung MC; Chan AO
    J Clin Res Pediatr Endocrinol; 2016 Sep; 8(3):356-9. PubMed ID: 27125267
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Transient pseudo-hypoaldosteronism following resection of the ileum: normal level of lymphocytic aldosterone receptors outside the acute phase.
    Vantyghem MC; Hober C; Evrard A; Ghulam A; Lescut D; Racadot A; Triboulet JP; Armanini D; Lefebvre J
    J Endocrinol Invest; 1999 Feb; 22(2):122-7. PubMed ID: 10195379
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Corticosterone methyl oxidase type II deficiency: a cause of failure to thrive and recurrent dehydration in early infancy.
    Picco P; Garibaldi L; Cotellessa M; DiRocco M; Borrone C
    Eur J Pediatr; 1992 Mar; 151(3):170-3. PubMed ID: 1601005
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Congenital hyperreninemic hypoaldosteronism unlinked to the aldosterone synthase (CYP11B2) gene.
    Kayes-Wandover KM; Tannin GM; Shulman D; Peled D; Jones KL; Karaviti L; White PC
    J Clin Endocrinol Metab; 2001 Nov; 86(11):5379-82. PubMed ID: 11701710
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Molecular Analysis of the CYP11B2 Gene in 62 Patients with Hypoaldosteronism Due to Aldosterone Synthase Deficiency.
    Merakou C; Fylaktou I; Sertedaki A; Dracopoulou M; Voutetakis A; Efthymiadou A; Christoforidis A; Dacou-Voutetakis C; Chrysis D; Kanaka-Gantenbein C
    J Clin Endocrinol Metab; 2021 Jan; 106(1):e182-e191. PubMed ID: 33098647
    [TBL] [Abstract][Full Text] [Related]  

  • 12. [Neonates with pseudohypoaldosteronism].
    Kleizen KJ; Claahsen-van der Grinten HL; Schulte EO; Creemers DG; Koster-Kamphuis L; Draaisma JM
    Ned Tijdschr Geneeskd; 2010; 154():A1485. PubMed ID: 20735869
    [No Abstract]   [Full Text] [Related]  

  • 13. High aldosterone and cortisol levels in salt wasting congenital adrenal hyperplasia: a clinical conundrum.
    Boddu SK; Madhavan S
    J Pediatr Endocrinol Metab; 2017 Nov; 30(12):1327-1331. PubMed ID: 29127765
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Aldosterone synthase deficiency and related disorders.
    White PC
    Mol Cell Endocrinol; 2004 Mar; 217(1-2):81-7. PubMed ID: 15134805
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Aldosterone synthase deficiency type II: an unusual presentation of the first Greek case reported with confirmed genetic analysis.
    Papailiou S; Vlachopapadopoulou EA; Sertedaki A; Maritsi D; Syggelos N; Syggelou A
    Endocr Regul; 2020 Jul; 54(3):227-229. PubMed ID: 32857717
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Two novel mutations of the CYP11B2 gene in a Japanese patient with aldosterone deficiency type 1.
    Kondo E; Nakamura A; Homma K; Hasegawa T; Yamaguchi T; Narugami M; Hattori T; Aoyagi H; Ishizu K; Tajima T
    Endocr J; 2013; 60(1):51-5. PubMed ID: 23018980
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Pseudohypoaldosteronism: mineralocorticoid unresponsiveness syndrome.
    Jaruratanasirikul S; Janjindamai W
    J Med Assoc Thai; 2000 Aug; 83(8):948-52. PubMed ID: 10998851
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Molecular genetic studies in a case series of isolated hypoaldosteronism due to biosynthesis defects or aldosterone resistance.
    Turan I; Kotan LD; Tastan M; Gurbuz F; Topaloglu AK; Yuksel B
    Clin Endocrinol (Oxf); 2018 Jun; 88(6):799-805. PubMed ID: 29582446
    [TBL] [Abstract][Full Text] [Related]  

  • 19. A novel CYP11B2 gene mutation in an Asian family with aldosterone synthase deficiency.
    Løvås K; McFarlane I; Nguyen HH; Curran S; Schwabe J; Halsall D; Bernhardt R; Wallace AM; Chatterjee VK
    J Clin Endocrinol Metab; 2009 Mar; 94(3):914-9. PubMed ID: 19116236
    [TBL] [Abstract][Full Text] [Related]  

  • 20. The enigma of pseudohypoaldosteronism.
    Zennaro MC; Borensztein P; Soubrier F; Armanini D; Corvol P
    Steroids; 1994 Feb; 59(2):96-9. PubMed ID: 8191555
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 15.