메뉴 건너뛰기




Volumn 325, Issue 2, 2003, Pages 93-97

A patient with sodium- and potassium-losing nephropathy

Author keywords

Renal potassium wasting; Renal salt wasting; Renal sodium wasting; Secondary hyperaldosteronism

Indexed keywords

POTASSIUM CHLORIDE; SODIUM CHLORIDE;

EID: 0037329250     PISSN: 00029629     EISSN: None     Source Type: Journal    
DOI: 10.1097/00000441-200302000-00006     Document Type: Article
Times cited : (1)

References (22)
  • 3
  • 4
    • 0002627262 scopus 로고
    • Renal failure simulating adrenocortical insufficiency
    • Thorn GW, Koepf GF, Clinton M Jr. Renal failure simulating adrenocortical insufficiency. N Eng J Med 1944;231: 76-85.
    • (1944) N Eng J Med , vol.231 , pp. 76-85
    • Thorn, G.W.1    Koepf, G.F.2    Clinton M., Jr.3
  • 5
    • 0020791456 scopus 로고
    • Salt-losing nephropathy. Clinical presentation and mechanisms
    • Uribarri J, Oh MS, Carroll HJ. Salt-losing nephropathy. Clinical presentation and mechanisms. Am J Nephrol 1983; 3:193-8.
    • (1983) Am J Nephrol , vol.3 , pp. 193-198
    • Uribarri, J.1    Oh, M.S.2    Carroll, H.J.3
  • 6
    • 0035208413 scopus 로고    scopus 로고
    • Inherited primary renal tubular hypokalemic alkalosis: A review of Gitelman and Bartter syndromes
    • Shaer AJ. Inherited primary renal tubular hypokalemic alkalosis: a review of Gitelman and Bartter syndromes. Am J Med Sci 2001;322:316-32.
    • (2001) Am J Med Sci , vol.322 , pp. 316-332
    • Shaer, A.J.1
  • 7
    • 16944366243 scopus 로고    scopus 로고
    • Mutations in the chloride channel gene, CLCNKB, cause Bartter's syndrome type III
    • Simon DB, Bindra RS, Mansfield TA, et al. Mutations in the chloride channel gene, CLCNKB, cause Bartter's syndrome type III. Nat Genet 1997;17:171-8.
    • (1997) Nat Genet , vol.17 , pp. 171-178
    • Simon, D.B.1    Bindra, R.S.2    Mansfield, T.A.3
  • 8
    • 0013375936 scopus 로고
    • Disturbances in water- and salt metabolism in the final stage of chronic renal insufficiency
    • Borst JR. Disturbances in water- and salt metabolism in the final stage of chronic renal insufficiency. Acta Med Scand 1949;136:1-8.
    • (1949) Acta Med Scand , vol.136 , pp. 1-8
    • Borst, J.R.1
  • 9
    • 0013924968 scopus 로고
    • Changes in plasma aldosterone, cortisol, corticosterone, and renin concentration in a patient with sodium-losing renal disease
    • Fraser R, James VHT, Brown JJ, et al. Changes in plasma aldosterone, cortisol, corticosterone, and renin concentration in a patient with sodium-losing renal disease. J Endocrinol 1966;35:311-20.
    • (1966) J Endocrinol , vol.35 , pp. 311-320
    • Fraser, R.1    James, V.H.T.2    Brown, J.J.3
  • 10
    • 0014236064 scopus 로고
    • Aldosterone secretion and sodium balance in salt-losing nephropathy
    • Walker WG, Jost LJ, Kowarski A, et al. Aldosterone secretion and sodium balance in salt-losing nephropathy. Johns Hopkins Med J 1968;122:45-54.
    • (1968) Johns Hopkins Med J , vol.122 , pp. 45-54
    • Walker, W.G.1    Jost, L.J.2    Kowarski, A.3
  • 11
    • 0013420411 scopus 로고
    • Low potassium syndrome due to defective renal tubular mechanisms for handling potassium
    • Earle DP, Sherry S, Eichna LW, et al. Low potassium syndrome due to defective renal tubular mechanisms for handling potassium. Am J Med 1951;11:282-301.
    • (1951) Am J Med , vol.11 , pp. 282-301
    • Earle, D.P.1    Sherry, S.2    Eichna, L.W.3
  • 12
    • 84939411511 scopus 로고
    • Salt loss in chronic renal disease
    • Read AE. Salt loss in chronic renal disease. Br Med J 1957;i:1399-401.
    • (1957) Br Med J , vol.1 , pp. 1399-1401
    • Read, A.E.1
  • 13
    • 0014677431 scopus 로고
    • Periarteritis nodosa associated with salt-losing nephritis
    • Karetzky MS. Periarteritis nodosa associated with salt-losing nephritis. N Y State J Med 1969;69:1329-33.
    • (1969) N Y State J Med , vol.69 , pp. 1329-1333
    • Karetzky, M.S.1
  • 14
    • 0029951224 scopus 로고    scopus 로고
    • The molecular basis of inherited hypokalemic alkalosis: Bartter's and Gitelman's syndromes
    • Simon DB, Lifton RP. The molecular basis of inherited hypokalemic alkalosis: Bartter's and Gitelman's syndromes. Am J Physiol 1996;271:F961-966.
    • (1996) Am J Physiol , vol.271
    • Simon, D.B.1    Lifton, R.P.2
  • 15
    • 0031779521 scopus 로고    scopus 로고
    • Bartter and related syndromes: The puzzle is almost solved
    • Rodriquez-Soriano J. Bartter and related syndromes: the puzzle is almost solved. Pediatr Nephrol 1998;12:315-27.
    • (1998) Pediatr Nephrol , vol.12 , pp. 315-327
    • Rodriquez-Soriano, J.1
  • 16
    • 0000142802 scopus 로고
    • Muscular paralysis and electrocardiographic abnormalities
    • Brown MR, Currens JH, Marchand JF. Muscular paralysis and electrocardiographic abnormalities. JAMA 1944;124: 545-9.
    • (1944) JAMA , vol.124 , pp. 545-549
    • Brown, M.R.1    Currens, J.H.2    Marchand, J.F.3
  • 18
    • 0016205903 scopus 로고
    • Familial hypokalemia associated with renal interstitial fibrosis
    • Potter WZ, Trygstad CW, Helmer OM, et al. Familial hypokalemia associated with renal interstitial fibrosis. Am J Med 1974;57:971-7.
    • (1974) Am J Med , vol.57 , pp. 971-977
    • Potter, W.Z.1    Trygstad, C.W.2    Helmer, O.M.3
  • 19
    • 0018873373 scopus 로고
    • Hyperreninemia, lysozymuria, and erythrocytosis in Fanconi syndrome with medullary cystic kidney
    • Fyhrquist FY, Klockars M, Gordin A, et al. Hyperreninemia, lysozymuria, and erythrocytosis in Fanconi syndrome with medullary cystic kidney. Acta Med Scand 1980;207:359-65.
    • (1980) Acta Med Scand , vol.207 , pp. 359-365
    • Fyhrquist, F.Y.1    Klockars, M.2    Gordin, A.3
  • 21
    • 0025022684 scopus 로고
    • Association of hypokalemia, aldosteronism, and renal cysts
    • Torres VE, Young WF, Offord KP, et al. Association of hypokalemia, aldosteronism, and renal cysts. N Engl J Med 1990;322:345-351.
    • (1990) N Engl J Med , vol.322 , pp. 345-351
    • Torres, V.E.1    Young, W.F.2    Offord, K.P.3
  • 22
    • 0033914432 scopus 로고    scopus 로고
    • Mutations in the chloride channel gene CLCNKB as a cause of classic Bartter syndrome
    • Konrad M, Vollmer M, Lemmink HH, et al. Mutations in the chloride channel gene CLCNKB as a cause of classic Bartter syndrome. J Am Soc Nephrol 2000;11:1449-59.
    • (2000) J Am Soc Nephrol , vol.11 , pp. 1449-1459
    • Konrad, M.1    Vollmer, M.2    Lemmink, H.H.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.