-
1
-
-
0039878875
-
Disorders of potassium metabolism
-
Schrier RW, ed. Lippincot-Raven, Philadelphia
-
Peterson LN, Levi M. Disorders of potassium metabolism. In: Schrier RW, ed. Renal and Electrolyte Disorders. Lippincot-Raven, Philadelphia, 1997: 192-240
-
(1997)
Renal and Electrolyte Disorders
, pp. 192-240
-
-
Peterson, L.N.1
Levi, M.2
-
3
-
-
0019991723
-
Surreptitious diuretic ingestion and pseudo-Bartter's syndrome
-
Jamison RL, Ross JC, Kempson RL, Sufit CR, Parker TE. Surreptitious diuretic ingestion and pseudo-Bartter's syndrome. Am J Med 1982; 73: 142-147
-
(1982)
Am J Med
, vol.73
, pp. 142-147
-
-
Jamison, R.L.1
Ross, J.C.2
Kempson, R.L.3
Sufit, C.R.4
Parker, T.E.5
-
4
-
-
0029906224
-
The Na-(K)-CL cotransporter family in the mammalian kidney: Molecular identification and function(s)
-
Delpire E, Kaplan MR, Plotkin MD, Hebert SC. The Na-(K)-Cl cotransporter family in the mammalian kidney: molecular identification and function(s). Nephrol Dial Transplant 1996; 11: 1967-1973
-
(1996)
Nephrol Dial Transplant
, vol.11
, pp. 1967-1973
-
-
Delpire, E.1
Kaplan, M.R.2
Plotkin, M.D.3
Hebert, S.C.4
-
5
-
-
0018344362
-
Metabolic mimicry of Bartter's syndrome by covert vomiting
-
Veldhuis JD, Bardin CW, Demers LM. Metabolic mimicry of Bartter's syndrome by covert vomiting. Am J Med 1979; 66: 361-363
-
(1979)
Am J Med
, vol.66
, pp. 361-363
-
-
Veldhuis, J.D.1
Bardin, C.W.2
Demers, L.M.3
-
6
-
-
50849151835
-
Hyperplasia of the juxtaglomerular complex with hyperaldosteronism and hypokalcmic alkalosis. A new syndrome
-
Bartter FC, Pronove P, Gill JR, MacCardle RC. Hyperplasia of the juxtaglomerular complex with hyperaldosteronism and hypokalcmic alkalosis. A new syndrome. Am J Med 1962; 33: 811-822
-
(1962)
Am J Med
, vol.33
, pp. 811-822
-
-
Bartter, F.C.1
Pronove, P.2
Gill, J.R.3
MacCardle, R.C.4
-
7
-
-
84993911692
-
Hypercalciuria in potassiumlosing nephropathy: A variant of Bartter's syndrome
-
Mac Credie DA, Rotenberg E, Williams AL. Hypercalciuria in potassiumlosing nephropathy: a variant of Bartter's syndrome. Aust Paediatr J 1974; 10: 286-295
-
(1974)
Aust Paediatr J
, vol.10
, pp. 286-295
-
-
Mac Credie, D.A.1
Rotenberg, E.2
Williams, A.L.3
-
8
-
-
0017597726
-
Furosemide-induced reduction in ionized calcium in hypoparathyroid patients
-
Gabow PA, Hanson T, Popovtzer M, Schrier RW. Furosemide-induced reduction in ionized calcium in hypoparathyroid patients. Ann Intern Med 1977; 86: 579-581
-
(1977)
Ann Intern Med
, vol.86
, pp. 579-581
-
-
Gabow, P.A.1
Hanson, T.2
Popovtzer, M.3
Schrier, R.W.4
-
9
-
-
0023242296
-
Characteristics and functions of Na-K-2CL cotransport in epithelial tissues
-
O'Grady SM, Palfrey HC, Field M. Characteristics and functions of Na-K-2Cl cotransport in epithelial tissues. Am J Physiol 1987; 253: C177
-
(1987)
Am J Physiol
, vol.253
-
-
O'Grady, S.M.1
Palfrey, H.C.2
Field, M.3
-
10
-
-
0030032699
-
Bartter's syndrome, hypokalemic alkalosis with hypercalciuria, is caused by mutations in the Na-K-2CL cotransporter NKCC2
-
Simon DB, Karet FE, Handam JM, Di Pietro A, Sanjad SA, Liftonn RP. Bartter's syndrome, hypokalemic alkalosis with hypercalciuria, is caused by mutations in the Na-K-2Cl cotransporter NKCC2. Nature Genet 1996; 13: 183-188
-
(1996)
Nature Genet
, vol.13
, pp. 183-188
-
-
Simon, D.B.1
Karet, F.E.2
Handam, J.M.3
Di Pietro, A.4
Sanjad, S.A.5
Liftonn, R.P.6
-
12
-
-
16944366243
-
Mutations in the chloride channel gene, CLCNKB, cause Bartter's syndrome type III
-
Simon BD, Bindra RS, Mansfield TA et al. Mutations in the chloride channel gene, CLCNKB, cause Bartter's syndrome type III. Nature Genet 1997; 17: 171-178
-
(1997)
Nature Genet
, vol.17
, pp. 171-178
-
-
Simon, B.D.1
Bindra, R.S.2
Mansfield, T.A.3
-
13
-
-
0029051359
-
Bartters's syndrome: The unsolved puzzle
-
Clive DM. Bartters's syndrome: the unsolved puzzle. Am J Kidney Dis 1995; 25: 813-823
-
(1995)
Am J Kidney Dis
, vol.25
, pp. 813-823
-
-
Clive, D.M.1
-
14
-
-
0013976561
-
A new familial disorder characterized by hypokalemia and hypomagnesemia
-
Gitelman HJ, Graham JB, Welt LG. A new familial disorder characterized by hypokalemia and hypomagnesemia. Trans Assoc Am Phys 1966; 79: 221-235
-
(1966)
Trans Assoc Am Phys
, vol.79
, pp. 221-235
-
-
Gitelman, H.J.1
Graham, J.B.2
Welt, L.G.3
-
15
-
-
0026512508
-
Use of calcium excretion values to distinguish two forms of primary renal tubular hypokalemic alkalosis: Bartter and gitelman syndromes
-
Bettinelli A, Bianchetti MG, Girardin E et al. Use of calcium excretion values to distinguish two forms of primary renal tubular hypokalemic alkalosis: Bartter and Gitelman syndromes. J Pediatr 1992; 20: 38-43
-
(1992)
J Pediatr
, vol.20
, pp. 38-43
-
-
Bettinelli, A.1
Bianchetti, M.G.2
Girardin, E.3
-
16
-
-
0029093611
-
Chronic hypokalaemia of adults: Gitelman's syndrome is frequent but classical Bartter's syndrome is rare
-
Gladziwa U, Schwartz R, Gitter AH et al. Chronic hypokalaemia of adults: Gitelman's syndrome is frequent but classical Bartter's syndrome is rare. Nephrol Dial Transplant 1995; 10: 1607-1613
-
(1995)
Nephrol Dial Transplant
, vol.10
, pp. 1607-1613
-
-
Gladziwa, U.1
Schwartz, R.2
Gitter, A.H.3
-
17
-
-
0027405688
-
Primary structure and functional expression of a cDNA encoding the thiazide-sensitive sodium cotransportcr
-
Gamba G, Saltzburg SN, Lombardi M et al. Primary structure and functional expression of a cDNA encoding the thiazide-sensitive sodium cotransportcr. Proc Natl Acad Sci USA 1993; 90: 2749
-
(1993)
Proc Natl Acad Sci USA
, vol.90
, pp. 2749
-
-
Gamba, G.1
Saltzburg, S.N.2
Lombardi, M.3
-
18
-
-
9044235777
-
Gitelman's variant of Bartter's syndrome, inherited hypokalemic alkalosis, is caused by mutations in the thiazidc-sensitivc Na-CL cotransporter
-
Simon DB, Nelson-Wiliams C, Johnson-Bia M et al. Gitelman's variant of Bartter's syndrome, inherited hypokalemic alkalosis, is caused by mutations in the thiazidc-sensitivc Na-Cl cotransporter. Nature Genet 1996; 12: 24-30
-
(1996)
Nature Genet
, vol.12
, pp. 24-30
-
-
Simon, D.B.1
Nelson-Wiliams, C.2
Johnson-Bia, M.3
-
19
-
-
0019495809
-
Prostaglandins and Bartter's syndrome
-
Dunn MJ. Prostaglandins and Bartter's syndrome. Kidney Int 1981; 19: 86-102
-
(1981)
Kidney Int
, vol.19
, pp. 86-102
-
-
Dunn, M.J.1
-
20
-
-
0027326953
-
Immune-related potassium-losing interstitial nephritis: A comparison with distal renal tubular acidosis
-
Wrong OM, Feest TG, Maciver AG. Immune-related potassium-losing interstitial nephritis: a comparison with distal renal tubular acidosis. Q J Med 1993; 86: 513-534
-
(1993)
Q J Med
, vol.86
, pp. 513-534
-
-
Wrong, O.M.1
Feest, T.G.2
Maciver, A.G.3
-
21
-
-
0023115717
-
Interstitial nephritis and primary biliary cirrhosis; a new association?
-
MacDougall IC, Isles CJ, Whitworth JA, More IAR, MacSween RNM. Interstitial nephritis and primary biliary cirrhosis; a new association? Clin Nephrol 1987; 27: 36-40
-
(1987)
Clin Nephrol
, vol.27
, pp. 36-40
-
-
MacDougall, I.C.1
Isles, C.J.2
Whitworth, J.A.3
More, I.A.R.4
MacSween, R.N.M.5
-
22
-
-
0000841496
-
Hypokalemic nephropathy in rat and man. A light and electron microscopic study
-
Muehrcke RC, Rosen S. Hypokalemic nephropathy in rat and man. A light and electron microscopic study. Lab Invest 1964; 13: 1359-1373
-
(1964)
Lab Invest
, vol.13
, pp. 1359-1373
-
-
Muehrcke, R.C.1
Rosen, S.2
|