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 *

132 related articles for article (PubMed ID: 11174838)

  • 21. An inherited defect in aldosterone biosynthesis caused by a mutation in or near the gene for steroid 11-hydroxylase.
    Globerman H; Rösler A; Theodor R; New MI; White PC
    N Engl J Med; 1988 Nov; 319(18):1193-7. PubMed ID: 3262827
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Congenitally defective aldosterone biosynthesis in humans: the involvement of point mutations of the P-450C18 gene (CYP11B2) in CMO II deficient patients.
    Mitsuuchi Y; Kawamoto T; Naiki Y; Miyahara K; Toda K; Kuribayashi I; Orii T; Yasuda K; Miura K; Nakao K
    Biochem Biophys Res Commun; 1992 Jan; 182(2):974-9. PubMed ID: 1346492
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Disorders of the aldosterone synthase and steroid 11beta-hydroxylase deficiencies.
    Peter M; Dubuis JM; Sippell WG
    Horm Res; 1999; 51(5):211-22. PubMed ID: 10559665
    [TBL] [Abstract][Full Text] [Related]  

  • 24. The constant plasma 18-hydroxycorticosterone to aldosterone ratio: an expression of the efficacy of corticosterone methyloxidase type II activity in disorders with variable aldosterone production.
    Kater CE; Biglieri EG; Rost CR; Schambelan M; Hirai J; Chang BC; Brust N
    J Clin Endocrinol Metab; 1985 Feb; 60(2):225-8. PubMed ID: 2981240
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Congenital hypoaldosteronism: the Visser-Cost syndrome revisited.
    Peter M; Sippell WG
    Pediatr Res; 1996 Mar; 39(3):554-60. PubMed ID: 8929880
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Type 1 aldosterone synthase deficiency presenting in a middle-aged man.
    Kayes-Wandover KM; Schindler RE; Taylor HC; White PC
    J Clin Endocrinol Metab; 2001 Mar; 86(3):1008-12. PubMed ID: 11238478
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Inborn error in the terminal step of aldosterone biosynthesis. Corticosterone methyl oxidase tpe II deficiency in a North American pedigree.
    Veldhuis JD; Kulin HE; Santen RJ; Wilson TE; Melby JC
    N Engl J Med; 1980 Jul; 303(3):117-21. PubMed ID: 6991942
    [TBL] [Abstract][Full Text] [Related]  

  • 28. 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]  

  • 29. Gene conversion in the CYP11B2 gene encoding P450c11AS is associated with, but does not cause, the syndrome of corticosterone methyloxidase II deficiency.
    Fardella CE; Hum DW; Rodriguez H; Zhang G; Barry FL; Ilicki A; Bloch CA; Miller WL
    J Clin Endocrinol Metab; 1996 Jan; 81(1):321-6. PubMed ID: 8550772
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Defective aldosterone synthesis associated with hyperkalemic periodic paralysis.
    Allen DB
    Arch Neurol; 1993 Mar; 50(3):325-8. PubMed ID: 8442715
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Acquired partial corticosterone methyl oxidase type II defect in diabetes mellitus. Case of hyperreninemic hypoaldosteronism.
    Braithwaite SS; Barbato AL; Emanuele MA
    Diabetes Care; 1990 Jul; 13(7):790-2. PubMed ID: 2167193
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Aldosterone synthase deficiency type I: hormonal and genetic analyses of two cases.
    López-Siguero JP; García-García E; Peter M; Sippell WG
    Horm Res; 1999; 52(6):298-300. PubMed ID: 10965212
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Analysis of novel heterozygous mutations in the CYP11B2 gene causing congenital aldosterone synthase deficiency and literature review.
    Miao H; Yu Z; Lu L; Zhu H; Auchus RJ; Liu J; Jiang J; Pan H; Gong F; Chen S; Lu Z
    Steroids; 2019 Oct; 150():108448. PubMed ID: 31302112
    [TBL] [Abstract][Full Text] [Related]  

  • 34. The impact of the clinical CYP11B2 mutation V386A strongly depends on the enzyme's genetic background.
    Neunzig J; Khatri Y; Bernhardt R
    Endocr J; 2017 Apr; 64(4):457-461. PubMed ID: 28190867
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Novel CYP11B2 mutation causing aldosterone synthase (P450c11AS) deficiency.
    Klomchan T; Supornsilchai V; Wacharasindhu S; Shotelersuk V; Sahakitrungruang T
    Eur J Pediatr; 2012 Oct; 171(10):1559-62. PubMed ID: 22801770
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Five novel mutations in CYP11B2 gene detected in patients with aldosterone synthase deficiency type I: Functional characterization and structural analyses.
    Nguyen HH; Hannemann F; Hartmann MF; Malunowicz EM; Wudy SA; Bernhardt R
    Mol Genet Metab; 2010 Aug; 100(4):357-64. PubMed ID: 20494601
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Mutations in aldosterone synthase gene of Milan hypertensive rats: phenotypic consequences.
    Lloyd-MacGilp SA; Torielli L; Bechtel S; Tripodi G; Gomez-Sanchez CE; Zagato L; Bernhardt R; Kenyon CJ
    Am J Physiol Endocrinol Metab; 2002 Mar; 282(3):E608-17. PubMed ID: 11832364
    [TBL] [Abstract][Full Text] [Related]  

  • 38. 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]  

  • 39. A compound heterozygote case of type II aldosterone synthase deficiency.
    Dunlop FM; Crock PA; Montalto J; Funder JW; Curnow KM
    J Clin Endocrinol Metab; 2003 Jun; 88(6):2518-26. PubMed ID: 12788848
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Severe hypoaldosteronism due to corticosterone methyl oxidase type II deficiency in two boys: metabolic and gas chromatography-mass spectrometry studies.
    Hauffa BP; Sólyom J; Gláz E; Shackleton CH; Wambach G; Vecsei P; Stolecke H; Homoki J
    Eur J Pediatr; 1991 Jan; 150(3):149-53. PubMed ID: 2044581
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 7.