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 *

107 related articles for article (PubMed ID: 830445)

  • 1. Selective hypoaldosteronism in Iranian Jews: An autosomal recessive trait.
    Cohen T; Theodor R; Rösler A
    Clin Genet; 1977 Jan; 11(1):25-30. PubMed ID: 830445
    [TBL] [Abstract][Full Text] [Related]  

  • 2. The nature of the defect in a salt-wasting disorder in Jews of Iran.
    Rösler A; Rabinowitz D; Theodor R; Ramirez LC; Ulick S
    J Clin Endocrinol Metab; 1977 Feb; 44(2):279-91. PubMed ID: 838841
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Metabolic responses to the administration of angiotensin II, K and ACTH in two salt-wasting syndromes.
    Rösler A; Theodor R; Boichis H; Gerty R; Ulick S; Alagem M; Tabachinik E; Cohen B; Rabinowitz D
    J Clin Endocrinol Metab; 1977 Feb; 44(2):292-301. PubMed ID: 190253
    [TBL] [Abstract][Full Text] [Related]  

  • 4. HLA in a selective aldosterone biosynthetic defect due to type 2 corticosterone methyl-oxidase deficiency.
    Brautbar C; Theodor R; Sack J; Levene C; Dupont B; Levine LS; Sharon R; Smaller S; Cohen T; Rösler A
    Tissue Antigens; 1981 Feb; 17(2):212-6. PubMed ID: 7233416
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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]  

  • 6. Isolated aldosterone deficiency in man: acquired and inborn errors in the biosynthesis or action of aldosterone.
    Veldhuis JD; Melby JC
    Endocr Rev; 1981; 2(4):495-517. PubMed ID: 6273148
    [No Abstract]   [Full Text] [Related]  

  • 7. Hereditary disorders among Iranian Jews.
    Zlotogora J
    Am J Med Genet; 1995 Jul; 58(1):32-7. PubMed ID: 7573153
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Apparently dominant transmission of a recessive disease: deficiency of factor VII in Iranian Jews.
    Tagliabue L; Duca F; Peyvandi F
    Ann Ital Med Int; 2000; 15(4):263-6. PubMed ID: 11202627
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Genetic screening in the Persian Jewish community: A pilot study.
    Kaback M; Lopatequi J; Portuges AR; Quindipan C; Pariani M; Salimpour-Davidov N; Rimoin DL
    Genet Med; 2010 Oct; 12(10):628-33. PubMed ID: 20733503
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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]  

  • 11. Autosomal recessive colobomatous microphthalmia.
    Zlotogora J; Legum C; Raz J; Merin S; BenEzra D
    Am J Med Genet; 1994 Feb; 49(3):261-2. PubMed ID: 8209881
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Mutations in the human CYP11B2 (aldosterone synthase) gene causing corticosterone methyloxidase II deficiency.
    Pascoe L; Curnow KM; Slutsker L; Rösler A; White PC
    Proc Natl Acad Sci U S A; 1992 Jun; 89(11):4996-5000. PubMed ID: 1594605
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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; 62(1):225-9. PubMed ID: 3510001
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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; 58(1):143-8. PubMed ID: 6315756
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Type 2 corticosterone methyloxidase defect in a 2-year-old Iranian Jewish child.
    Buchta RM
    Am J Dis Child; 1984 Dec; 138(12):1154. PubMed ID: 6507399
    [No Abstract]   [Full Text] [Related]  

  • 16. Selective hypoaldosteronism due to combined defects of the conversion from inactive renin to active renin and the aldosterone biosynthesis from corticosterone.
    Muto S; Akai Y; Ono S; Kusano E; Asano Y
    Nephron; 2001 Jul; 88(3):247-53. PubMed ID: 11423756
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Hyporeninemic hypoaldosteronism associated with acquired immune deficiency syndrome.
    Kalin MF; Poretsky L; Seres DS; Zumoff B
    Am J Med; 1987 May; 82(5):1035-8. PubMed ID: 3555065
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Hyporeninemic hypoaldosteronism in infancy.
    Monnens L; Fiselier T; Bos B; van Munster P
    Nephron; 1983; 35(2):140-2. PubMed ID: 6353255
    [TBL] [Abstract][Full Text] [Related]  

  • 19. High frequency of atypical pseudocholinesterase gene among Iraqi and Iranian Jews.
    Szeinberg A; Pipano S; Assa M; Medalie JH; Neufeld HN
    Clin Genet; 1972; 3(2):123-7. PubMed ID: 5054314
    [No Abstract]   [Full Text] [Related]  

  • 20. Plasma corticosteroids in hyperreninemic hypoaldosteronism: evidence for diffuse impairment of the zona glomerulosa.
    Stern N; Beck FW; Sowers JR; Tuck M; Hsueh WA; Zipser RD
    J Clin Endocrinol Metab; 1983 Jul; 57(1):217-20. PubMed ID: 6304133
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.