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Journal Abstract Search

105 related items for PubMed ID: 3175608

  • 1. Aldosterone deficiency in infancy.
    Glass IA, Wallace AM, Beattie TJ.
    Scott Med J; 1988 Jun; 33(3):275-6. PubMed ID: 3175608
    [Abstract] [Full Text] [Related]

  • 2. Congenital hypoaldosteronism.
    Sethupathi V, Vijayakumar M, Janakiraman L, Nammalwar BR.
    Indian Pediatr; 2008 Aug; 45(8):695-7. PubMed ID: 18723916
    [Abstract] [Full Text] [Related]

  • 3. Congenital hyperreninemic hypoaldosteronism due to aldosterone synthase deficiency type I in a Portuguese patient - Case report and review of literature.
    Lages AS, Vale B, Oliveira P, Cardoso R, Dinis I, Carrilho F, Mirante A.
    Arch Endocrinol Metab; 2019 Feb; 63(1):84-88. PubMed ID: 30864636
    [Abstract] [Full Text] [Related]

  • 4. Aldosterone synthesis in salt-wasting congenital adrenal hyperplasia with complete absence of adrenal 21-hydroxylase.
    Speiser PW, Agdere L, Ueshiba H, White PC, New MI.
    N Engl J Med; 1991 Jan 17; 324(3):145-9. PubMed ID: 1984191
    [Abstract] [Full Text] [Related]

  • 5. [Salt losing syndrome in the new-born. New diagnostic approach. Report of our experience between 1960 and 1976].
    Limal JM, Rappaport R, Lenoir G.
    Ann Pediatr (Paris); 1977 Jan 17; 24(1):49-55. PubMed ID: 16211944
    [No Abstract] [Full Text] [Related]

  • 6. Hyporeninemic hypoaldosteronism in infancy: a familial disease.
    Landier F, Guyene TT, Boutignon H, Nahoul K, Corvol P, Job JC.
    J Clin Endocrinol Metab; 1984 Jan 17; 58(1):143-8. PubMed ID: 6315756
    [Abstract] [Full Text] [Related]

  • 7. 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 17; 86(11):5379-82. PubMed ID: 11701710
    [Abstract] [Full Text] [Related]

  • 8. Plasma renin activity in the management of congenital adrenal hyperplasia.
    Griffiths KD, Anderson JM, Rudd BT, Virdi NK, Holder G, Rayner PH.
    Arch Dis Child; 1984 Apr 17; 59(4):360-5. PubMed ID: 6372706
    [Abstract] [Full Text] [Related]

  • 9. [Clinical use of fludrocortisone acetate in congenital adrenal hyperplasia. Effect on plasma renin activity and aldosterone (author's transl)].
    Tokuhiro E, Suwa S, Maesaka H.
    Horumon To Rinsho; 1980 Apr 17; 28(3):345-51. PubMed ID: 6994941
    [No Abstract] [Full Text] [Related]

  • 10. Hyporeninemic hypoaldosteronism, sodium wasting and mineralocorticoid-resistant hyperkalemia in two patients with obstructive uropathy.
    Pelleya R, Oster JR, Perez GO.
    Am J Nephrol; 1983 Apr 17; 3(4):223-7. PubMed ID: 6351617
    [Abstract] [Full Text] [Related]

  • 11. Pseudohypoaldosteronism without nephropathy masking salt-wasting congenital adrenal hyperplasia genetically confirmed.
    Balcells C, Gili T, Pérez J, Corripio R.
    BMJ Case Rep; 2013 Jan 30; 2013():. PubMed ID: 23370958
    [Abstract] [Full Text] [Related]

  • 12. Biochemical diagnosis and management of corticosterone methyl oxidase type II deficiency.
    Lee PD, Patterson BD, Hintz RL, Rosenfeld RG.
    J Clin Endocrinol Metab; 1986 Jan 30; 62(1):225-9. PubMed ID: 3510001
    [Abstract] [Full Text] [Related]

  • 13. The Aldosterone/Renin Ratio as a Diagnostic Tool for the Diagnosis of Primary Hypoaldosteronism in Newborns and Infants.
    Ruecker B, Lang-Muritano M, Spanaus K, Welzel M, l'Allemand D, Phan-Hug F, Katschnig C, Konrad D, Holterhus PM, Schoenle EJ.
    Horm Res Paediatr; 2015 Jan 30; 84(1):43-8. PubMed ID: 25968592
    [Abstract] [Full Text] [Related]

  • 14. Congenital primary adrenal insufficiency and selective aldosterone defects presenting as salt-wasting in infancy: a single center 10-year experience.
    Bizzarri C, Olivini N, Pedicelli S, Marini R, Giannone G, Cambiaso P, Cappa M.
    Ital J Pediatr; 2016 Aug 02; 42(1):73. PubMed ID: 27485500
    [Abstract] [Full Text] [Related]

  • 15. Salt losing nephropathy simulating congenital adrenal hyperplasia in an infant.
    Kari JA, Bamashmous HA, Al-Agha AE, Mosli HA.
    Saudi Med J; 2002 Jul 02; 23(7):863-5. PubMed ID: 12174243
    [Abstract] [Full Text] [Related]

  • 16. [Four cases of aldosterone synthase deficiency in childhood].
    Collinet E, Pelissier P, Richard O, Gay C, Pugeat M, Morel Y, Stephan JL.
    Arch Pediatr; 2012 Nov 02; 19(11):1191-5. PubMed ID: 23062999
    [Abstract] [Full Text] [Related]

  • 17. Homozygosity for a mutation in the CYP11B2 gene in an infant with congenital corticosterone methyl oxidase deficiency type II.
    Jessen CL, Christensen JH, Birkebaek NH, Rittig S.
    Acta Paediatr; 2012 Nov 02; 101(11):e519-25. PubMed ID: 22931312
    [Abstract] [Full Text] [Related]

  • 18. Aldosterone-to-renin ratio as a marker for disease severity in 21-hydroxylase deficiency congenital adrenal hyperplasia.
    Nimkarn S, Lin-Su K, Berglind N, Wilson RC, New MI.
    J Clin Endocrinol Metab; 2007 Jan 02; 92(1):137-42. PubMed ID: 17032723
    [Abstract] [Full Text] [Related]

  • 19. Multisteroid analysis in children with terminal aldosterone biosynthesis defects.
    Peter M, Partsch CJ, Sippell WG.
    J Clin Endocrinol Metab; 1995 May 02; 80(5):1622-7. PubMed ID: 7745009
    [Abstract] [Full Text] [Related]

  • 20. Cross-reactivity of adrenal steroids with aldosterone may prevent the accurate diagnosis of congenital adrenal hyperplasia.
    Tuhan HU, Catli G, Anik A, Onay H, Dundar B, Bober E, Abaci A.
    J Pediatr Endocrinol Metab; 2015 May 02; 28(5-6):701-4. PubMed ID: 25503463
    [Abstract] [Full Text] [Related]

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