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Volumn 181, Issue 4, 2004, Pages 513-521

Pharmacotyping of hypokalaemic salt-losing tubular disorders

Author keywords

Bartter syndrome; Gitelman syndrome; Hyperprostaglandin E syndrome; Pharmacotyping; Salt losing tubular disorders; Terminology

Indexed keywords

AMILORIDE; CHLORIDE CHANNEL; FUROSEMIDE; POTASSIUM CHANNEL; SODIUM POTASSIUM CHLORIDE COTRANSPORTER; THIAZIDE DIURETIC AGENT;

EID: 4043121815     PISSN: 00016772     EISSN: None     Source Type: Journal    
DOI: 10.1111/j.1365-201X.2004.01325.x     Document Type: Conference Paper
Times cited : (44)

References (47)
  • 1
    • 0022415262 scopus 로고
    • 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 scopus 로고
    • 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 scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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
  • 13
    • 0031584084 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고
    • 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
  • 28
    • 0024814270 scopus 로고
    • 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 scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고
    • 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 scopus 로고
    • 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
  • 38
    • 0022251369 scopus 로고
    • 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 scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고
    • 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 scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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


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