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Journal Abstract Search

236 related items for PubMed ID: 9587067

  • 21. Aquaporin-2 water channel mutations causing nephrogenic diabetes insipidus.
    van Os CH, Deen PM.
    Proc Assoc Am Physicians; 1998; 110(5):395-400. PubMed ID: 9756089
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  • 23. Molecular biology of diabetes insipidus.
    Fujiwara TM, Morgan K, Bichet DG.
    Annu Rev Med; 1995; 46():331-43. PubMed ID: 7541187
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  • 24. Autosomal recessive nephrogenic diabetes insipidus caused by an aquaporin-2 mutation.
    Hochberg Z, Van Lieburg A, Even L, Brenner B, Lanir N, Van Oost BA, Knoers NV.
    J Clin Endocrinol Metab; 1997 Feb; 82(2):686-9. PubMed ID: 9024277
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  • 30. Identification and characterization of aquaporin-2 water channel mutations causing nephrogenic diabetes insipidus with partial vasopressin response.
    Canfield MC, Tamarappoo BK, Moses AM, Verkman AS, Holtzman EJ.
    Hum Mol Genet; 1997 Oct; 6(11):1865-71. PubMed ID: 9302264
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  • 33. Normal fibrinolytic responses to 1-desamino-8-D-arginine vasopressin in patients with nephrogenic diabetes insipidus caused by mutations in the aquaporin 2 gene.
    van Lieburg AF, Knoers VV, Mallmann R, Proesmans W, van den Heuvel LP, Monnens LA.
    Nephron; 1996 Oct; 72(4):544-6. PubMed ID: 8730418
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  • 35. [Hereditary nephrogenic diabetes insipidus].
    Morin D, Ala Y, Dumas R.
    Arch Pediatr; 1995 Jun; 2(6):560-7. PubMed ID: 7640759
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  • 37. Nephrogenic diabetes insipidus: essential insights into the molecular background and potential therapies for treatment.
    Moeller HB, Rittig S, Fenton RA.
    Endocr Rev; 2013 Apr; 34(2):278-301. PubMed ID: 23360744
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  • 40. [Vasopressin type 2 receptor mutations in congenital diabetes insipidus].
    Tsukaguchi H, Matsubara H, Inada M.
    Nihon Rinsho; 1998 Jul; 56(7):1848-55. PubMed ID: 9702064
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