-
1
-
-
0022415262
-
Pseudo-Bartter's syndrome and surreptitious abuse of furosemide in a woman complicated with masked idiopathic edema and defective character
-
Ando, A., Koshida, H., Morise, T. et al. 1985. Pseudo-Bartter's syndrome and surreptitious abuse of furosemide in a woman complicated with masked idiopathic edema and defective character. Nippon Jinzo Gakkai Shi 27, 519-524.
-
(1985)
Nippon Jinzo Gakkai Shi
, vol.27
, pp. 519-524
-
-
Ando, A.1
Koshida, H.2
Morise, T.3
-
2
-
-
50849151835
-
Hyperplasia of the juxtaglomerular complex with hyperaldosteronism and hypokalemic alkalosis - A new syndrome
-
Bartter, F.C., Pronove, P., Gill, J.R.J., MacCardle, R.C. & Diller, E. 1962. Hyperplasia of the juxtaglomerular complex with hyperaldosteronism and hypokalemic alkalosis - a new syndrome. Am J Med 33, 811-828.
-
(1962)
Am J Med
, vol.33
, pp. 811-828
-
-
Bartter, F.C.1
Pronove, P.2
Gill, J.R.J.3
MacCardle, R.C.4
Diller, E.5
-
3
-
-
0017096787
-
Prostaglandins are overproduced by the kidneys and mediate hyperreninemia in Bartter's syndrome
-
Bartter, F.C., Gill, J.R. Jr, Frolich, J.C. et al. 1976. Prostaglandins are overproduced by the kidneys and mediate hyperreninemia in Bartter's syndrome. Trans Assoc Am Physicians 89, 77-91.
-
(1976)
Trans Assoc Am Physicians
, vol.89
, pp. 77-91
-
-
Bartter, F.C.1
Gill Jr., J.R.2
Frolich, J.C.3
-
4
-
-
0032012889
-
Hyperplasia of the juxtaglomerular complex with hyperaldosteronism and hypokalemic alkalosis. A new syndrome 1962
-
Bartter, F.C., Pronove, P., Gill, J.R. Jr. et al. 1998. Hyperplasia of the juxtaglomerular complex with hyperaldosteronism and hypokalemic alkalosis. A new syndrome 1962. J Am Soc Nephrol 9, 516-528.
-
(1998)
J Am Soc Nephrol
, vol.9
, pp. 516-528
-
-
Bartter, F.C.1
Pronove, P.2
Gill Jr., J.R.3
-
5
-
-
0026512508
-
Use of calcium excretion values to distinguish two forms of primary renal tubular hypokalemic alkalosis: Bartter and Gitelman syndromes
-
Bettinelli, A., Bianchetti, M.G., Girardin, E. et al. 1992. Use of calcium excretion values to distinguish two forms of primary renal tubular hypokalemic alkalosis: Bartter and Gitelman syndromes. J Pediatr 120, 38-43.
-
(1992)
J Pediatr
, vol.120
, pp. 38-43
-
-
Bettinelli, A.1
Bianchetti, M.G.2
Girardin, E.3
-
6
-
-
0032791379
-
Gitelman disease associated with growth hormone deficiency, disturbances in vasopressin secretion and empty sella: A new hereditary renal tubular-pituitary syndrome?
-
Bettinelli, A., Rusconi, R., Ciarmatori, S. et al. 1999. Gitelman disease associated with growth hormone deficiency, disturbances in vasopressin secretion and empty sella: a new hereditary renal tubular-pituitary syndrome? Pediatr Res 46, 232-238.
-
(1999)
Pediatr Res
, vol.46
, pp. 232-238
-
-
Bettinelli, A.1
Rusconi, R.2
Ciarmatori, S.3
-
7
-
-
0035189356
-
Mutation of BSND causes Bartter syndrome with sensorineural deafness and kidney failure
-
Birkenhager, R., Otto, E., Schurmann, M.J. et al. 2001. Mutation of BSND causes Bartter syndrome with sensorineural deafness and kidney failure. Nat Genet 29, 310-314.
-
(2001)
Nat Genet
, vol.29
, pp. 310-314
-
-
Birkenhager, R.1
Otto, E.2
Schurmann, M.J.3
-
8
-
-
0028301822
-
Discrepancy between lithium and free water clearance in patients with Bartter's syndrome
-
Boer, W.H., Hené, R.J., Koomans, H.A. & Dorhout Mees, E.J. 1994. Discrepancy between lithium and free water clearance in patients with Bartter's syndrome. Nephron 67, 82-87.
-
(1994)
Nephron
, vol.67
, pp. 82-87
-
-
Boer, W.H.1
Hené, R.J.2
Koomans, H.A.3
Dorhout Mees, E.J.4
-
9
-
-
0031937693
-
Linkage of infantile Bartter syndrome with sensorineural deafness to chromosome 1p
-
Brennan, T.M., Landau, D., Shalev, H. et al. 1998. Linkage of infantile Bartter syndrome with sensorineural deafness to chromosome 1p. Am J Hum Genet 62, 355-361.
-
(1998)
Am J Hum Genet
, vol.62
, pp. 355-361
-
-
Brennan, T.M.1
Landau, D.2
Shalev, H.3
-
10
-
-
84940140364
-
Distal nephron function in Bartter's syndrome: Abnormal conductance to chloride in the cortical collecting tubule?
-
Colussi, G., Rombola, G., Verde, G. et al. 1992. Distal nephron function in Bartter's syndrome: abnormal conductance to chloride in the cortical collecting tubule? Am J Nephrol 12, 229-239.
-
(1992)
Am J Nephrol
, vol.12
, pp. 229-239
-
-
Colussi, G.1
Rombola, G.2
Verde, G.3
-
11
-
-
0035136314
-
Gitelman's syndrome revisited: An evaluation of symptoms and health-related quality of life
-
Cruz, D.N., Shaer, A.J., Bia, M.J., Lifton, R.P. & Simon, D.B. 2001. Gitelman's syndrome revisited: an evaluation of symptoms and health-related quality of life. Kidney Int 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
-
12
-
-
0018816444
-
The clinical entity of pseudo-Bartter's syndrome
-
Demers, L.M., Veldhuis, J.D. & Ramos, E. 1980. The clinical entity of pseudo-Bartter's syndrome. Adv Prostaglandin Thromboxane Res 7, 1203-1206.
-
(1980)
Adv Prostaglandin Thromboxane Res
, vol.7
, pp. 1203-1206
-
-
Demers, L.M.1
Veldhuis, J.D.2
Ramos, E.3
-
13
-
-
0031584084
-
Mutations in the ROMK gene in antenatal Bartter syndrome are associated with impaired K+ channel function
-
Derst, C., Konrad, M., Kockerling, A. et al. 1997. Mutations in the ROMK gene in antenatal Bartter syndrome are associated with impaired K+ channel function. Biochem Biophys Res Commun 230, 641-645.
-
(1997)
Biochem Biophys Res Commun
, vol.230
, pp. 641-645
-
-
Derst, C.1
Konrad, M.2
Kockerling, A.3
-
14
-
-
0035969520
-
Barttin is a Cl-channel beta-subunit crucial for renal Cl- reabsorption and inner ear K+ secretion
-
Estevez, R., Boettger, T., Stein, V. et al. 2001. Barttin is a Cl-channel beta-subunit crucial for renal Cl- reabsorption and inner ear K+ secretion. Nature 414, 558-561.
-
(2001)
Nature
, vol.414
, pp. 558-561
-
-
Estevez, R.1
Boettger, T.2
Stein, V.3
-
15
-
-
0015069866
-
Chronic Hypokalaemia with growth retardation, normotensive hyperrenin-hyperaldosteronism ('Bartter's syndrome'), and hypercalciuria. Report of two cases with emphasis on natural history and on catch-up growth during treatment
-
Fanconi, A., Schachenmann, G., Nüssli, R. & Prader, A. 1971. Chronic Hypokalaemia with growth retardation, normotensive hyperrenin- hyperaldosteronism ('Bartter's syndrome'), and hypercalciuria. Report of two cases with emphasis on natural history and on catch-up growth during treatment. Helv Paediat Acta 2, 144-163.
-
(1971)
Helv Paediat Acta
, vol.2
, pp. 144-163
-
-
Fanconi, A.1
Schachenmann, G.2
Nüssli, R.3
Prader, A.4
-
16
-
-
0037339228
-
Transient neonatal hyperkalemia in the antenatal (ROMK defective) Bartter syndrome
-
Finer, G., Shalev, H., Birk, O.S. et al. 2003. Transient neonatal hyperkalemia in the antenatal (ROMK defective) Bartter syndrome. J Pediatr 142, 318-323.
-
(2003)
J Pediatr
, vol.142
, pp. 318-323
-
-
Finer, G.1
Shalev, H.2
Birk, O.S.3
-
17
-
-
0013976561
-
A new familial disorder characterized by hypokalemia and hypomagnesemia
-
Gitelman, H.J., Graham, J.B. & Welt, L.G. 1966. A new familial disorder characterized by hypokalemia and hypomagnesemia. Trans Assoc Am Physicians 79, 221-223.
-
(1966)
Trans Assoc Am Physicians
, vol.79
, pp. 221-223
-
-
Gitelman, H.J.1
Graham, J.B.2
Welt, L.G.3
-
18
-
-
0036727962
-
Induction of fetal diuresis with intraamniotic furosemide increases the clearance of intraamniotic substances: An alternative therapy aimed at reducing intraamniotic meconium concentration
-
Hakguder, G., Ates, O., Olguner, M. et al. 2002. Induction of fetal diuresis with intraamniotic furosemide increases the clearance of intraamniotic substances: an alternative therapy aimed at reducing intraamniotic meconium concentration. J Pediatr Surg 37, 1337-1342.
-
(2002)
J Pediatr Surg
, vol.37
, pp. 1337-1342
-
-
Hakguder, G.1
Ates, O.2
Olguner, M.3
-
19
-
-
8044222737
-
Mutations in the gene encoding the inwardly-rectifying renal potassium channel, ROMK, cause the antenatal variant of Bartter syndrome: Evidence for genetic heterogeneity. International Collaborative Study Group for Bartter-like Syndromes
-
International Study Group for Bartter-like syndromes, Károlyi, L., Konrad, M. et al. 1997. Mutations in the gene encoding the inwardly-rectifying renal potassium channel, ROMK, cause the antenatal variant of Bartter syndrome: evidence for genetic heterogeneity. International Collaborative Study Group for Bartter-like Syndromes. Hum Mol Genet 6, 17-26.
-
(1997)
Hum Mol Genet
, vol.6
, pp. 17-26
-
-
Károlyi, L.1
Konrad, M.2
-
20
-
-
0033667558
-
Mutations in the chloride channel gene, CLCNKB, leading to a mixed Bartter-Gitelman phenotype
-
Jeck, N., Konrad, M., Peters, M. et al. 2000. Mutations in the chloride channel gene, CLCNKB, leading to a mixed Bartter-Gitelman phenotype. Pediatr Res 48, 754-758.
-
(2000)
Pediatr Res
, vol.48
, pp. 754-758
-
-
Jeck, N.1
Konrad, M.2
Peters, M.3
-
21
-
-
0035408815
-
Hypokalemic salt-losing tubulopathy with chronic renal failure and sensorineural deafness
-
Jeck, N., Reinalter, S.C., Henne, T. et al. 2001. Hypokalemic salt-losing tubulopathy with chronic renal failure and sensorineural deafness. Pediatrics 108, E5.
-
(2001)
Pediatrics
, vol.108
-
-
Jeck, N.1
Reinalter, S.C.2
Henne, T.3
-
22
-
-
0035512256
-
Low sodium and furosemide-induced stimulation of the renin system in man is mediated by cyclooxygenase 2
-
Kammerl, M.C., Nusing, R.M., Schweda, F. et al. 2001. Low sodium and furosemide-induced stimulation of the renin system in man is mediated by cyclooxygenase 2. Clin Pharmacol Ther 70, 468-474.
-
(2001)
Clin Pharmacol Ther
, vol.70
, pp. 468-474
-
-
Kammerl, M.C.1
Nusing, R.M.2
Schweda, F.3
-
23
-
-
0027523016
-
Hemodynamic and fluid responses to furosemide infusion in the ovine fetus
-
Kelly, T.F., Moore, T.R. & Brace, R.A. 1993. Hemodynamic and fluid responses to furosemide infusion in the ovine fetus. Am J Obstet Gynecol 168, 260-268.
-
(1993)
Am J Obstet Gynecol
, vol.168
, pp. 260-268
-
-
Kelly, T.F.1
Moore, T.R.2
Brace, R.A.3
-
24
-
-
0030357628
-
Impaired response to furosemide in hyperprostaglandin E syndrome: Evidence for a tubular defect in the loop of Henle
-
Kockerling, A., Reinalter, S.C. & Seyberth, H.W. 1996. Impaired response to furosemide in hyperprostaglandin E syndrome: evidence for a tubular defect in the loop of Henle. J Pediatr 129, 519-528.
-
(1996)
J Pediatr
, vol.129
, pp. 519-528
-
-
Kockerling, A.1
Reinalter, S.C.2
Seyberth, H.W.3
-
25
-
-
0033914432
-
Mutations in the chloride channel gene CLCNKB as a cause of classic Bartter syndrome
-
Konrad, M., Vollmer, M., Lemmink, H.H. et al. 2000. Mutations in the chloride channel gene CLCNKB as a cause of classic Bartter syndrome. J Am Soc Nephrol 11, 1449-1459.
-
(2000)
J Am Soc Nephrol
, vol.11
, pp. 1449-1459
-
-
Konrad, M.1
Vollmer, M.2
Lemmink, H.H.3
-
26
-
-
0028787681
-
Infantile variant of Bartter syndrome and sensorineural deafness: A new autosomal recessive disorder
-
Landau, D., Shalev, H., Ohaly, M. & Carmi, R. 1995. Infantile variant of Bartter syndrome and sensorineural deafness: a new autosomal recessive disorder. Am J Med Genet 59, 454-459.
-
(1995)
Am J Med Genet
, vol.59
, pp. 454-459
-
-
Landau, D.1
Shalev, H.2
Ohaly, M.3
Carmi, R.4
-
27
-
-
0015228360
-
Potassium-losing nephropathy of childhood
-
McCredie, D.A., Blair-West, J.R., Scoggins, B.A. & Shipman, R. 1971. Potassium-losing nephropathy of childhood. Med J Aust 1, 129-135.
-
(1971)
Med J Aust
, vol.1
, pp. 129-135
-
-
McCredie, D.A.1
Blair-West, J.R.2
Scoggins, B.A.3
Shipman, R.4
-
28
-
-
0024814270
-
Furosemide directly stimulates prostaglandin E2 production in the thick ascending limb of Henle's loop
-
Miyanoshita, A., Terada, M. & Endou, H. 1989. Furosemide directly stimulates prostaglandin E2 production in the thick ascending limb of Henle's loop. J Pharmacol Exp Ther 251, 1155-1159.
-
(1989)
J Pharmacol Exp Ther
, vol.251
, pp. 1155-1159
-
-
Miyanoshita, A.1
Terada, M.2
Endou, H.3
-
29
-
-
0021528921
-
A variant of Bartter's syndrome. Bartter's syndrome associated with hydramnios, prematurity, hypercalciuria and nephrocalcinosis
-
Ohlsson, A., Sieck, U., Cumming, W., Akhtar, M. & Serenius, F. 1984. A variant of Bartter's syndrome. Bartter's syndrome associated with hydramnios, prematurity, hypercalciuria and nephrocalcinosis. Acta Paediatr Scand 73, 868-874.
-
(1984)
Acta Paediatr Scand
, vol.73
, pp. 868-874
-
-
Ohlsson, A.1
Sieck, U.2
Cumming, W.3
Akhtar, M.4
Serenius, F.5
-
30
-
-
0037082531
-
Clinical presentation of genetically defined patients with hypokalemic salt-losing tubulopathies
-
Peters, M., Jeck, N., Reinalter, S. et al. 2002. Clinical presentation of genetically defined patients with hypokalemic salt-losing tubulopathies. Am J Med 112, 183-190.
-
(2002)
Am J Med
, vol.112
, pp. 183-190
-
-
Peters, M.1
Jeck, N.2
Reinalter, S.3
-
31
-
-
0042366195
-
Luminal NaCl delivery regulates basolateral PGE2 release from macula densa cells
-
Peti-Peterdi, J., Komlosi, P., Fuson, A.L. et al. 2003. Luminal NaCl delivery regulates basolateral PGE2 release from macula densa cells. J Clin Invest 112, 76-82.
-
(2003)
J Clin Invest
, vol.112
, pp. 76-82
-
-
Peti-Peterdi, J.1
Komlosi, P.2
Fuson, A.L.3
-
32
-
-
0023680022
-
Variant of Bartter's syndrome with a distal tubular rather than loop of Henle defect
-
Puschett, J.B., Greenberg, A., Mitro, R., Piraino, B. & Wallia, R. 1988. Variant of Bartter's syndrome with a distal tubular rather than loop of Henle defect. Nephron 50, 205-211.
-
(1988)
Nephron
, vol.50
, pp. 205-211
-
-
Puschett, J.B.1
Greenberg, A.2
Mitro, R.3
Piraino, B.4
Wallia, R.5
-
33
-
-
0031949627
-
Neonatal Bartter syndrome: Spontaneous resolution of all signs and symptoms
-
Reinalter, S., Devlieger, H. & Proesmans, W. 1998. Neonatal Bartter syndrome: spontaneous resolution of all signs and symptoms. Pediatr Nephrol 12, 186-188.
-
(1998)
Pediatr Nephrol
, vol.12
, pp. 186-188
-
-
Reinalter, S.1
Devlieger, H.2
Proesmans, W.3
-
34
-
-
0036318596
-
Role of cyclooxygenase-2 in hyperprostaglandin E syndrome/ante-natal Bartter syndrome
-
Reinalter, S.C., Jeck, N., Brochhausen, C. et al. 2002. Role of cyclooxygenase-2 in hyperprostaglandin E syndrome/ante-natal Bartter syndrome. Kidney Int 62, 253-260.
-
(2002)
Kidney Int
, vol.62
, pp. 253-260
-
-
Reinalter, S.C.1
Jeck, N.2
Brochhausen, C.3
-
35
-
-
0000487732
-
Persistent, probably congenital, hypokalemic metabolic alkalosis with hyaline degeneration of renal tubules and normal urinary aldosterone
-
Rosenbaum, P. & Hughes, M. 1957. Persistent, probably congenital, hypokalemic metabolic alkalosis with hyaline degeneration of renal tubules and normal urinary aldosterone (Abstract). Am J Dis Child 94, 560.
-
(1957)
Am J Dis Child
, vol.94
, pp. 560
-
-
Rosenbaum, P.1
Hughes, M.2
-
36
-
-
2042522547
-
L'hypokaliémie chronique idiopathique avec hyperkaliurie de l'enfant
-
Royer, P., Delaitre, R., Mathieu, H. et al. 1964. L'hypokaliémie chronique idiopathique avec hyperkaliurie de l'enfant. Rev Franc Etudes Clin et Biol, IX, 61-87.
-
(1964)
Rev Franc Etudes Clin et Biol
, vol.9
, pp. 61-87
-
-
Royer, P.1
Delaitre, R.2
Mathieu, H.3
-
37
-
-
0029616225
-
Pre-pubertal growth in the hyperprostaglandin E syndrome
-
Seidel, C., Reinalter, S., Seyberth, H.W. & Scharer, K. 1995. Pre-pubertal growth in the hyperprostaglandin E syndrome. Pediatr Nephrol 9, 723-728.
-
(1995)
Pediatr Nephrol
, vol.9
, pp. 723-728
-
-
Seidel, C.1
Reinalter, S.2
Seyberth, H.W.3
Scharer, K.4
-
38
-
-
0022251369
-
Congenital hypokalemia with hypercalciuria in preterm infants: A hyperprostaglandinuric tubular syndrome different from Bartter syndrome
-
Seyberth, H.W., Rascher, W., Schweer, H. et al. 1985. Congenital hypokalemia with hypercalciuria in preterm infants: a hyperprostaglandinuric tubular syndrome different from Bartter syndrome. J Pediatr 107, 694-701.
-
(1985)
J Pediatr
, vol.107
, pp. 694-701
-
-
Seyberth, H.W.1
Rascher, W.2
Schweer, H.3
-
39
-
-
0023588270
-
Role of prostaglandins in hyperprostaglandin E syndrome and in selected renal tubular disorders
-
Seyberth, H.W., Koniger, S.J., Rascher, W., Kuhl, P.G. & Schweer, H. 1987. Role of prostaglandins in hyperprostaglandin E syndrome and in selected renal tubular disorders. Pediatr Nephrol 1, 491-497.
-
(1987)
Pediatr Nephrol
, vol.1
, pp. 491-497
-
-
Seyberth, H.W.1
Koniger, S.J.2
Rascher, W.3
Kuhl, P.G.4
Schweer, H.5
-
40
-
-
0030032699
-
Bartter's syndrome, hypokalaemic alkalosis with hypercalciuria, is caused by mutations in the Na-K-2Cl cotransporter NKCC2
-
Simon, D.B., Karet, F.E., Hamdan, J.M. et al. 1996a. Bartter's syndrome, hypokalaemic alkalosis with hypercalciuria, is caused by mutations in the Na-K-2Cl cotransporter NKCC2. Nat Genet 13, 183-188.
-
(1996)
Nat Genet
, vol.13
, pp. 183-188
-
-
Simon, D.B.1
Karet, F.E.2
Hamdan, J.M.3
-
41
-
-
0029794875
-
Genetic heterogeneity of Bartter's syndrome revealed by mutations in the K+ channel, ROMK
-
Simon, D.E., Karet, F.E., Rodriguez-Soriano, J. et al. 1996b. Genetic heterogeneity of Bartter's syndrome revealed by mutations in the K+ channel, ROMK. Nat Genet 14, 152-156.
-
(1996)
Nat Genet
, vol.14
, pp. 152-156
-
-
Simon, D.E.1
Karet, F.E.2
Rodriguez-Soriano, J.3
-
42
-
-
9044235777
-
Gitelman's variant of Bartter's syndrome, inherited hypokalaemic alkalosis, is caused by mutations in the thiazide-sensitive Na-Cl cotransporter
-
Simon, D.B., Nelson-Williams, C., Bia, M.J. et al. 1996c. Gitelman's variant of Bartter's syndrome, inherited hypokalaemic alkalosis, is caused by mutations in the thiazide-sensitive Na-Cl cotransporter. Nat Genet 12, 24-30.
-
(1996)
Nat Genet
, vol.12
, pp. 24-30
-
-
Simon, D.B.1
Nelson-Williams, C.2
Bia, M.J.3
-
43
-
-
16944366243
-
Mutations in the chloride channel gene, CLCNKB, cause Bartter's syndrome type III
-
Simon, D.E., Bindra, R.S., Mansfield, T.A. et al. 1997. Mutations in the chloride channel gene, CLCNKB, cause Bartter's syndrome type III. Nat Genet 17, 171-178.
-
(1997)
Nat Genet
, vol.17
, pp. 171-178
-
-
Simon, D.E.1
Bindra, R.S.2
Mansfield, T.A.3
-
44
-
-
0026482217
-
Bartter's syndrome: Evidence suggesting a distal tubular defect in a hypocalciuric variant of the syndrome
-
Sutton, R.A., Mavichak, V., Halabe, A. & Wilkins, G.E. 1992. Bartter's syndrome: evidence suggesting a distal tubular defect in a hypocalciuric variant of the syndrome. Miner Electrolyte Metab 18, 43-51.
-
(1992)
Miner Electrolyte Metab
, vol.18
, pp. 43-51
-
-
Sutton, R.A.1
Mavichak, V.2
Halabe, A.3
Wilkins, G.E.4
-
45
-
-
0017286809
-
Bartter's syndrome with hyperplasia of renomedullary cells: Successful treatment with indomethacin
-
Verberckmoes, R., van Damme, B.B., Clement, J., Amery, A. & Michielsen, P. 1976. Bartter's syndrome with hyperplasia of renomedullary cells: successful treatment with indomethacin. Kidney Int 9, 302-307.
-
(1976)
Kidney Int
, vol.9
, pp. 302-307
-
-
Verberckmoes, R.1
Van Damme, B.B.2
Clement, J.3
Amery, A.4
Michielsen, P.5
-
46
-
-
0036452353
-
Barttin increases surface expression and changes current properties of ClC-K channels
-
Waldegger, S., Jeck, N., Barth, P. et al. 2002. Barttin increases surface expression and changes current properties of ClC-K channels. Pflugers Arch 444, 411-418.
-
(2002)
Pflugers Arch
, vol.444
, pp. 411-418
-
-
Waldegger, S.1
Jeck, N.2
Barth, P.3
-
47
-
-
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. 2003. A novel mutation in the chloride channel gene, CLCNKB, as a cause of Gitelman and Bartter syndromes. Kidney Int 63, 24-32.
-
(2003)
Kidney Int
, vol.63
, pp. 24-32
-
-
Zelikovic, I.1
Szargel, R.2
Hawash, A.3
|