-
1
-
-
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; 120: 38-43
-
(1992)
J Pediatr
, vol.120
, pp. 38-43
-
-
Bettinelli, A.1
Bianchetti, M.G.2
Girardin, E.3
-
3
-
-
0028356071
-
Correction of hypokalemia with anti-aldosterone therapy in Gitelmans's syndrome
-
Colussi G, Rombola G, De Ferrari ME, Macaluso M, Minetti L. Correction of hypokalemia with anti-aldosterone therapy in Gitelmans's syndrome. Amer J Nephrol 1994; 14: 127-135
-
(1994)
Amer J Nephrol
, vol.14
, pp. 127-135
-
-
Colussi, G.1
Rombola, G.2
De Ferrari, M.E.3
Macaluso, M.4
Minetti, L.5
-
4
-
-
0035136314
-
Gitelman's syndrome revisited: An evaluation of symptoms and health-related quality of life
-
Cruz DN, Shaer AJ, Bia MJ, Lifton RP, Simon DB. Gitelman's syndrome revisited: An evaluation of symptoms and health-related quality of life. Kidney Int 2001; 59: 710-717
-
(2001)
Kidney Int
, vol.59
, pp. 710-717
-
-
Cruz, D.N.1
Shaer, A.J.2
Bia, M.J.3
Lifton, R.P.4
Simon, D.B.5
-
5
-
-
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 Physicians 1966; 79: 221-235
-
(1966)
Trans Assoc Physicians
, vol.79
, pp. 221-235
-
-
Gitelman, H.J.1
Graham, J.B.2
Welt, L.G.3
-
6
-
-
0025878027
-
Diagnostik und therapie bedrohlichef störungen des wasser- und elektrolythaushaltes
-
Kemmer FW, Plum J, Grabensee B. Diagnostik und Therapie bedrohlichef Störungen des Wasser- und Elektrolythaushaltes. Internist 1991; 32: 206-219
-
(1991)
Internist
, vol.32
, pp. 206-219
-
-
Kemmer, F.W.1
Plum, J.2
Grabensee, B.3
-
7
-
-
0007809443
-
Hereditäre tubulopathien mit diuretika-ähnlichem salzverlust
-
Köckerling A, Konrad M, Seyberth HW. Hereditäre Tubulopathien mit Diuretika-ähnlichem Salzverlust. Dt Ärztebl 1998; 95: A1841-1846
-
(1998)
Dt Ärztebl
, vol.95
-
-
Köckerling, A.1
Konrad, M.2
Seyberth, H.W.3
-
8
-
-
17144462641
-
Novel mutations in the thiazide-sensitive NaCl cotransporter gene in patients with Gitelman syndrome with predominant localization to the C-terminal domain
-
Lemmink HH, Knoers NVAM, Karolyi L et al. Novel mutations in the thiazide-sensitive NaCl cotransporter gene in patients with Gitelman syndrome with predominant localization to the C-terminal domain. Kidney Int 1998; 54: 720-730
-
(1998)
Kidney Int
, vol.54
, pp. 720-730
-
-
Lemmink, H.H.1
Knoers, N.V.A.M.2
Karolyi, L.3
-
9
-
-
0029972220
-
Novel molecular variants of the Na-Cl cotransporter gene are responsible for Gitelman Syndrome
-
Mastroianni N, Bettinelli A, Bianchetti M et al. Novel molecular variants of the Na-Cl cotransporter gene are responsible for Gitelman Syndrome. Am J Hum Genet 1996; 59: 1019-1026
-
(1996)
Am J Hum Genet
, vol.59
, pp. 1019-1026
-
-
Mastroianni, N.1
Bettinelli, A.2
Bianchetti, M.3
-
10
-
-
0032711678
-
Chronic, diagnosis-restistant hypokalaemia
-
Reimann D, Gross P. Chronic, diagnosis-restistant hypokalaemia. Nephrol Dial Transplant 1999; 14: 1957-2961
-
(1999)
Nephrol Dial Transplant
, vol.14
, pp. 1957-2961
-
-
Reimann, D.1
Gross, P.2
-
11
-
-
0023765041
-
Bartter's syndrome. A review of 28 patients followed for 10 years
-
Rudin A. Bartter's syndrome. A review of 28 patients followed for 10 years. Acta Med Scanc 1988; 224: 165-171
-
(1988)
Acta Med Scanc
, vol.224
, pp. 165-171
-
-
Rudin, A.1
-
12
-
-
9044235777
-
Gitelman's variant of Bartter's syndrome, inherited hypokalaemic alkalosis, is caused by mutations in the thiazide-sensitive Na-Cl cotransporter
-
Simon DB, Nelson-Williams C, Bia MJ et al. Gitelman's variant of Bartter's syndrome, inherited hypokalaemic alkalosis, is caused by mutations in the thiazide-sensitive Na-Cl cotransporter. Nature Genet 1996; 12: 24-30
-
(1996)
Nature Genet
, vol.12
, pp. 24-30
-
-
Simon, D.B.1
Nelson-Williams, C.2
Bia, M.J.3
-
13
-
-
0026482217
-
Bartter's syndrome: Evidence suggesting a distal tubular defect in a hypocalciuric variant of the syndrome
-
Sutton RAL, Mavichak V, Halabe A, Wilkins GE. Bartter's syndrome: Evidence suggesting a distal tubular defect in a hypocalciuric variant of the syndrome. Miner Electrol Metab 1992; 18: 43-51
-
(1992)
Miner Electrol Metab
, vol.18
, pp. 43-51
-
-
Sutton, R.A.L.1
Mavichak, V.2
Halabe, A.3
Wilkins, G.E.4
-
14
-
-
0028945391
-
Possible discrimination of Gitelman's syndrome from Bartter's syndrome by renal clearance study: Report of two cases
-
Tsukamoto T, Kobayashi T, Kawamoto, Fukase M, Chihara K. Possible discrimination of Gitelman's syndrome from Bartter's syndrome by renal clearance study: report of two cases. AJKD 1995; 25: 637-641
-
(1995)
AJKD
, vol.25
, pp. 637-641
-
-
Tsukamoto, T.1
Kobayashi, T.2
Kawamoto3
Fukase, M.4
Chihara, K.5
-
15
-
-
0037066446
-
28-Jähriger patient mit hypokaliämischer lähmung
-
Vogel A, Becker M, Lahmer R, Schneider J, Dirks H, Arnold W. 28-jähriger Patient mit hypokaliämischer Lähmung. Dtsch Med Wochenschr 2002; 127: 796-801
-
(2002)
Dtsch Med Wochenschr
, vol.127
, pp. 796-801
-
-
Vogel, A.1
Becker, M.2
Lahmer, R.3
Schneider, J.4
Dirks, H.5
Arnold, W.6
-
16
-
-
0037213896
-
A novel mutation in the chloride channel gene, CLCNKB, as a cause of Gitelman and Bartter syndromes
-
Zelikovic I, Szargel R, Hawash A et al. A novel mutation in the chloride channel gene, CLCNKB, as a cause of Gitelman and Bartter syndromes. Kidney Int 2003; 63: 24-32
-
(2003)
Kidney Int
, vol.63
, pp. 24-32
-
-
Zelikovic, I.1
Szargel, R.2
Hawash, A.3
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