-
1
-
-
50849151835
-
Hyperplasia of juxtaglomerular complex with hyperaldosteronism and hypokalemic alkalosis
-
Bartter FC, Pronove P, Gill JR Jr, MacCardle RC (1962) Hyperplasia of juxtaglomerular complex with hyperaldosteronism and hypokalemic alkalosis. Am J Med 33:811-828
-
(1962)
Am J Med
, vol.33
, pp. 811-828
-
-
Bartter, F.C.1
Pronove, P.2
Gill Jr., J.R.3
MacCardle, R.C.4
-
2
-
-
0029051359
-
Bartter's syndrome: The unsolved puzzle
-
Clive DM (1995) Bartter's syndrome: the unsolved puzzle. Am J Kidney Dis 25:813-823
-
(1995)
Am J Kidney Dis
, vol.25
, pp. 813-823
-
-
Clive, D.M.1
-
3
-
-
0028824342
-
Urinary chloride excretion distinguishes between renal and extrarenal metabolic alkalosis
-
Mersin SS, Ramelli GP, Laux-End R, Bianchetti MG (1995) Urinary chloride excretion distinguishes between renal and extrarenal metabolic alkalosis. Eur J Pediatr 154:979-982
-
(1995)
Eur J Pediatr
, vol.154
, pp. 979-982
-
-
Mersin, S.S.1
Ramelli, G.P.2
Laux-End, R.3
Bianchetti, M.G.4
-
4
-
-
0029612244
-
Concealed administration of frusemide simulating Bartter syndrome in a 4,5-year-old boy
-
D'Avanzo M, Santinelli R, Tolone C, Betinelli A, Bianchetti MG (1995) Concealed administration of frusemide simulating Bartter syndrome in a 4,5-year-old boy. Pediatr Nephrol 9:749-750
-
(1995)
Pediatr Nephrol
, vol.9
, pp. 749-750
-
-
D'Avanzo, M.1
Santinelli, R.2
Tolone, C.3
Betinelli, A.4
Bianchetti, M.G.5
-
5
-
-
0013976561
-
A new familial disorder characterized by hypokalemia and hypomagnesemia
-
Gitelman HJ, Graham JB, Welt LG (1966) A new familial disorder characterized by hypokalemia and hypomagnesemia. Trans Assoc Am Physicians 79:221-233
-
(1966)
Trans Assoc Am Physicians
, vol.79
, pp. 221-233
-
-
Gitelman, H.J.1
Graham, J.B.2
Welt, L.G.3
-
6
-
-
0029093611
-
Chronic hypokalaemia in adults: Gitelman syndrome is frequent but classical Bartter syndrome is rare
-
Gladziwa U, Schwarz R, Gitter AH, Bijman J, Seyberth H, Beck F, Ritz E, Gross P (1995) Chronic hypokalaemia in adults: Gitelman syndrome is frequent but classical Bartter syndrome is rare Nephiol Dial Transplant 10:1607-1613
-
(1995)
Nephiol Dial Transplant
, vol.10
, pp. 1607-1613
-
-
Gladziwa, U.1
Schwarz, R.2
Gitter, A.H.3
Bijman, J.4
Seyberth, H.5
Beck, F.6
Ritz, E.7
Gross, P.8
-
8
-
-
0026512508
-
Use of calcium excretion values to distinguish two forms of primary renal tubular hypokalemic alkalosis: Bartter and Gitelman syndromes
-
Bettenelli A, Bianchetti MG, Girardin E, Caringella A, Cecconi M, Appiani AC, Pavanello L, Gastaldi R, Isimbaldi C, Lama G, Marchesoni C, Mateucci C, Patriarca P, Di Natale B, Setzu C, Vitucci P (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
-
-
Bettenelli, A.1
Bianchetti, M.G.2
Girardin, E.3
Caringella, A.4
Cecconi, M.5
Appiani, A.C.6
Pavanello, L.7
Gastaldi, R.8
Isimbaldi, C.9
Lama, G.10
Marchesoni, C.11
Mateucci, C.12
Patriarca, P.13
Di Natale, B.14
Setzu, C.15
Vitucci, P.16
-
9
-
-
0019961848
-
Neonatal Bartter's syndrome, indomethacin and necrotizing enterocolitis
-
Marlow N, Chiswick ML (1982) Neonatal Bartter's syndrome, indomethacin and necrotizing enterocolitis. Acta Paediatr Scand 71:1031-1032
-
(1982)
Acta Paediatr Scand
, vol.71
, pp. 1031-1032
-
-
Marlow, N.1
Chiswick, M.L.2
-
11
-
-
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
-
12
-
-
0021966716
-
Bartter syndrome in two siblings - Antenal and neonatal observations
-
Proesmans W, Devlieger H, Van Assche A, Eggermont E, Vanderberghe K, Lemmens F, Sieprath P, Lijnen P (1985) Bartter syndrome in two siblings - antenal and neonatal observations. Int J Pediatr Nephrol 6:63-70
-
(1985)
Int J Pediatr Nephrol
, vol.6
, pp. 63-70
-
-
Proesmans, W.1
Devlieger, H.2
Van Assche, A.3
Eggermont, E.4
Vanderberghe, K.5
Lemmens, F.6
Sieprath, P.7
Lijnen, P.8
-
13
-
-
0022251369
-
Congenital hypokalemia with hypercalciuria in preterm infants: A hyperprostaglandinuric tubular syndrome different from Bartter syndrome
-
Seyberth HW, Rascher W, Schweer W, Kühl PG, Mehls O, Schärer K (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, W.3
Kühl, P.G.4
Mehls, O.5
Schärer, K.6
-
14
-
-
0015069866
-
Chronic hypokalemia 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, Nuessli R, Prader A (1971) Chronic hypokalemia 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 Paediatr Acta 6:144-163
-
(1971)
Helv Paediatr Acta
, vol.6
, pp. 144-163
-
-
Fanconi, A.1
Schachenmann, G.2
Nuessli, R.3
Prader, A.4
-
15
-
-
84993911692
-
Hypercalciuria in potassium-losing nephropathy: A variant of Bartter's syndrome
-
McCredie DA, Rotenberg W, Williams AL (1974) Hypercalciuria in potassium-losing nephropathy: a variant of Bartter's syndrome. Aust Paediatr J 10:286-295
-
(1974)
Aust Paediatr J
, vol.10
, pp. 286-295
-
-
McCredie, D.A.1
Rotenberg, W.2
Williams, A.L.3
-
16
-
-
0016565732
-
Bartter syndrome: Typical facies and normal plasma volume
-
James T, Holland NH, Preston D (1975) Bartter syndrome: typical facies and normal plasma volume Am J Dis Child 129:1205-1207
-
(1975)
Am J Dis Child
, vol.129
, pp. 1205-1207
-
-
James, T.1
Holland, N.H.2
Preston, D.3
-
17
-
-
0030202644
-
Variants of Bartter's syndrome
-
McCredie DA (1996) Variants of Bartter's syndrome. Pediatr Nephrol 10:419-421
-
(1996)
Pediatr Nephrol
, vol.10
, pp. 419-421
-
-
McCredie, D.A.1
-
18
-
-
0029951224
-
The molecular basis of inherited hypokalemic alkalosis: Bartter's and Gitelman's syndromes
-
Simon DB, Lifton RP (1996) The molecular basis of inherited hypokalemic alkalosis: Bartter's and Gitelman's syndromes. Am J Physiol 271:F961-F966
-
(1996)
Am J Physiol
, vol.271
-
-
Simon, D.B.1
Lifton, R.P.2
-
19
-
-
0030032699
-
Bartter's syndrome, hypokalaemic alkalosis with hypercalciuria, is caused by mutations in the Na-K-2Cl cotransporter NKCC2
-
Simon DB, Karet FE, Hamdan JM, Di Pietro A, Sanjad SA, Lifton RP (1996) 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
Di Pietro, A.4
Sanjad, S.A.5
Lifton, R.P.6
-
20
-
-
0029794875
-
+ channel, ROMK
-
+ channel, ROMK. Nat Genet 14:152-156
-
(1996)
Nat Genet
, vol.14
, pp. 152-156
-
-
Simon, D.B.1
Karet, F.E.2
Rodriguez-Soriano, J.3
Hamdan, J.H.4
Di Pietro, A.5
Trachtman, H.6
Sanjad, S.A.7
Lifton, R.P.8
-
21
-
-
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 (1997) Mutations in the gene encoding the inwardly-rectifying renal potassium channel, ROMK, cause the antenatal variant of Bartter syndrome: evidence for genetic heterogeneity. Hum Mol Genet 6:17-26
-
(1997)
Hum Mol Genet
, vol.6
, pp. 17-26
-
-
-
22
-
-
0042080700
-
New mutations in the gene for luminal potassium channel ROMK in neonatal Bartter syndrome
-
Vollmer M, Koehrer M, Topaloglu R, Brandis M, Hildebrandt F with the The International Collaborative Group for Bartter-like syndromes (1997) New mutations in the gene for luminal potassium channel ROMK in neonatal Bartter syndrome. Pediatric Nephrol 11:C48
-
(1997)
Pediatric Nephrol
, vol.11
-
-
Vollmer, M.1
Koehrer, M.2
Topaloglu, R.3
Brandis, M.4
Hildebrandt, F.5
-
23
-
-
0041579632
-
Atypical cases of the hypercalciuric variant of Bartter syndrome: Importance of molecular diagnosis
-
Betinnelli A, Casari G, Mastroianni N, Ciarmatori S, Leozappa G, De Logu A, Navone C, Cecconi M, Sereni F (1997) Atypical cases of the hypercalciuric variant of Bartter syndrome: importance of molecular diagnosis Pediatric Nephrol 11:C49
-
(1997)
Pediatric Nephrol
, vol.11
-
-
Betinnelli, A.1
Casari, G.2
Mastroianni, N.3
Ciarmatori, S.4
Leozappa, G.5
De Logu, A.6
Navone, C.7
Cecconi, M.8
Sereni, F.9
-
24
-
-
16944366243
-
Mutations in the chloride channel ClC-Kb cause Bartter's syndrome type III
-
Simon DB, Bindra RS, Nelson-Williams C, Mansfield TA, Mendonça E, Stone R, Schurmann S , Nayir A, Alpay H, Bakkaloglu A. Rodríguez-Soriano J, Morales JM, Sanjad SA, Taylor CM, Pilz D, Brem A, Trachtman H, Griswold W, Richard GA, John E, Lifton RP (1997) Mutations in the chloride channel ClC-Kb cause Bartter's syndrome type III. Nat Genet 17:171-178
-
(1997)
Nat Genet
, vol.17
, pp. 171-178
-
-
Simon, D.B.1
Bindra, R.S.2
Nelson-Williams, C.3
Mansfield, T.A.4
Mendonça, E.5
Stone, R.6
Schurmann, S.7
Nayir, A.8
Alpay, H.9
Bakkaloglu, A.10
Rodríguez-Soriano, J.11
Morales, J.M.12
Sanjad, S.A.13
Taylor, C.M.14
Pilz, D.15
Brem, A.16
Trachtman, H.17
Griswold, W.18
Richard, G.A.19
John, E.20
Lifton, R.P.21
more..
-
25
-
-
0030249306
-
Assignment of the genes encoding the human chloride channels, CLCNKA and CLCNKB, to 1p36 and of CLCN3 to 4q32-q33 by in situ hybridization
-
Saito-Ohara F, Uchida S, Takeuchi Y, Sasaki S, Hayashi A, Marumo F, Ikeuchi T (1996) Assignment of the genes encoding the human chloride channels, CLCNKA and CLCNKB, to 1p36 and of CLCN3 to 4q32-q33 by in situ hybridization. Genomics 36:372-374
-
(1996)
Genomics
, vol.36
, pp. 372-374
-
-
Saito-Ohara, F.1
Uchida, S.2
Takeuchi, Y.3
Sasaki, S.4
Hayashi, A.5
Marumo, F.6
Ikeuchi, T.7
-
26
-
-
0028788756
-
Cloning and characterization of CLCN5, the human kidney chloride channel gene implicated in Dent disease (an X-linked hereditary nephrolithiasis)
-
Fisher SE, Van Bakel I, Lloyd SE, Pearce SH, Thakker RV, Craig IW (1995) Cloning and characterization of CLCN5, the human kidney chloride channel gene implicated in Dent disease (an X-linked hereditary nephrolithiasis). Genomics 29:598-606
-
(1995)
Genomics
, vol.29
, pp. 598-606
-
-
Fisher, S.E.1
Van Bakel, I.2
Lloyd, S.E.3
Pearce, S.H.4
Thakker, R.V.5
Craig, I.W.6
-
27
-
-
0028907029
-
Genetic heterogeneity in tubular hypomagnesemia-hypokalemia with hypocalciuria (Gitelman's syndrome)
-
Betinelli A, Bianchetti MG, Borella P, Volpini E, Metta MG, Basilico E, Selicorni A, Bargellini A, Grassi MR (1995) Genetic heterogeneity in tubular hypomagnesemia-hypokalemia with hypocalciuria (Gitelman's syndrome). Kidney Int 47:547-551
-
(1995)
Kidney Int
, vol.47
, pp. 547-551
-
-
Betinelli, A.1
Bianchetti, M.G.2
Borella, P.3
Volpini, E.4
Metta, M.G.5
Basilico, E.6
Selicorni, A.7
Bargellini, A.8
Grassi, M.R.9
-
28
-
-
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, Ellison D, Karet FE, Morey Molina A, Vaara I, Iwata F, Cushner HM, Koolen M, Gainza FJ, Gitelman HL, Lifton RP (1996) 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
Ellison, D.4
Karet, F.E.5
Morey Molina, A.6
Vaara, I.7
Iwata, F.8
Cushner, H.M.9
Koolen, M.10
Gainza, F.J.11
Gitelman, H.L.12
Lifton, R.P.13
-
29
-
-
0029778992
-
Gitelman's syndrome is genetically distinct from other forms of Bartter's syndrome
-
Károlyi L, Ziegler A, Pollak M, Fischbach M, Grzeschik K-H, Koch MC, Seyberth HW (1996) Gitelman's syndrome is genetically distinct from other forms of Bartter's syndrome. Pediatr Nephrol 10:551-554
-
(1996)
Pediatr Nephrol
, vol.10
, pp. 551-554
-
-
Károlyi, L.1
Ziegler, A.2
Pollak, M.3
Fischbach, M.4
Grzeschik, K.-H.5
Koch, M.C.6
Seyberth, H.W.7
-
30
-
-
0029764485
-
Linkage of Gitelman syndrome to the thiazide-sensitive sodium-chloride cotransporter gene with identification of mutations in Dutch families
-
Lemmink HH, Heuvel LPWJ van den, Dijk HA van, Merkx GFM, Smilde TJ, Taschner PEM, Monnens LAH, Hebert SC, Knoers NVAM (1996) Linkage of Gitelman syndrome to the thiazide-sensitive sodium-chloride cotransporter gene with identification of mutations in Dutch families. Pediatr Nephrol 10:403-407
-
(1996)
Pediatr Nephrol
, vol.10
, pp. 403-407
-
-
Lemmink, H.H.1
Van Den Heuvel, L.P.W.J.2
Van Dijk, H.A.3
Merkx, G.F.M.4
Smilde, T.J.5
Taschner, P.E.M.6
Monnens, L.A.H.7
Hebert, S.C.8
Knoers, N.V.A.M.9
-
31
-
-
0029972220
-
Novel molecular variants of the Na-Cl cotransporter gene are responsible for Gitelman syndrome
-
Mastroianni N, Betinelli A, Bianchetti M, Colussi G, De Fusco M, Sereni F, Ballabio A, Casari G (1996) Novel molecular variants of the Na-Cl cotransporter gene are responsible for Gitelman syndrome. Am J Hum Genet 59:1019-1026
-
(1996)
Am J Hum Genet
, vol.59
, pp. 1019-1026
-
-
Mastroianni, N.1
Betinelli, A.2
Bianchetti, M.3
Colussi, G.4
De Fusco, M.5
Sereni, F.6
Ballabio, A.7
Casari, G.8
-
32
-
-
0030410932
-
Gitelman's syndrome (Bartter's variant) maps to the thiazide-sensitive cotransporter gene locus on chromosome 16q13 in a large kindred
-
Pollack MR, Delaney VB, Graham RM, Hebert SC (1996) Gitelman's syndrome (Bartter's variant) maps to the thiazide-sensitive cotransporter gene locus on chromosome 16q13 in a large kindred. J Am Soc Nephrol 7:2244-2248
-
(1996)
J Am Soc Nephrol
, vol.7
, pp. 2244-2248
-
-
Pollack, M.R.1
Delaney, V.B.2
Graham, R.M.3
Hebert, S.C.4
-
33
-
-
10544232272
-
Association of a mutation in thiazide-sensitive Na-Cl cotransporter with familial Gitelman's syndrome
-
Takeuchi K, Kure S, Kato T, Taniyama Y, Takahashi N, Ikeda Y, Abe T, Narisawa K, Muramatsu Y, Abe K (1996) Association of a mutation in thiazide-sensitive Na-Cl cotransporter with familial Gitelman's syndrome. J Clin Endocrinol Metab 81:4496-4499
-
(1996)
J Clin Endocrinol Metab
, vol.81
, pp. 4496-4499
-
-
Takeuchi, K.1
Kure, S.2
Kato, T.3
Taniyama, Y.4
Takahashi, N.5
Ikeda, Y.6
Abe, T.7
Narisawa, K.8
Muramatsu, Y.9
Abe, K.10
-
34
-
-
0030954698
-
Bartter syndrome and its neonatal variant
-
Proesmans W (1997) Bartter syndrome and its neonatal variant. Eur J Pediatr 156:669-679
-
(1997)
Eur J Pediatr
, vol.156
, pp. 669-679
-
-
Proesmans, W.1
-
35
-
-
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
-
36
-
-
0030918271
-
Bartter syndrome in Costa Rica: A description of 20 cases
-
Madrigal G, Saborio P, Mora F, Rincon G, Guay-Woodford L (1997) Bartter syndrome in Costa Rica: a description of 20 cases. Pediatr Nephrol 11:296-301
-
(1997)
Pediatr Nephrol
, vol.11
, pp. 296-301
-
-
Madrigal, G.1
Saborio, P.2
Mora, F.3
Rincon, G.4
Guay-Woodford, L.5
-
37
-
-
0023916322
-
Growth from birth to adulthood in a patient with the neonatal form of Bartter syndrome
-
Proesmans W, Massa G, Vanderschueren-Lodeweyckx M (1988) Growth from birth to adulthood in a patient with the neonatal form of Bartter syndrome. Pediatr Nephrol 2.205-209
-
(1988)
Pediatr Nephrol
, vol.2
, pp. 205-209
-
-
Proesmans, W.1
Massa, G.2
Vanderschueren-Lodeweyckx, M.3
-
38
-
-
0026536173
-
Calcium homeostasis and hypercalciuria in hyperprostaglandinism e syndrome
-
Leonhardt A, Timmermanns G, Roth B, Seyberth HW (1992) Calcium homeostasis and hypercalciuria in hyperprostaglandinism E syndrome. J Pediatr 120:546-554
-
(1992)
J Pediatr
, vol.120
, pp. 546-554
-
-
Leonhardt, A.1
Timmermanns, G.2
Roth, B.3
Seyberth, H.W.4
-
40
-
-
0042581669
-
Pre- and postnatal diagnosis of hyperprostaglandin e syndrome following molecular diagnosis from amniocytes
-
Konrad M, Köckerling A, Leonhardt A, Kärolyi L, Seyberth HW (1997) Pre- and postnatal diagnosis of hyperprostaglandin E syndrome following molecular diagnosis from amniocytes. J Am Soc Nephrol 8:90A
-
(1997)
J Am Soc Nephrol
, vol.8
-
-
Konrad, M.1
Köckerling, A.2
Leonhardt, A.3
Kärolyi, L.4
Seyberth, H.W.5
-
41
-
-
0029779337
-
A case of neonatal Bartter's syndrome
-
Wong W, Hulton SA, Taylor CM, Raafat F, Lote CJ, Lindop G (1996) A case of neonatal Bartter's syndrome. Pediatr Nephrol 10:414-418
-
(1996)
Pediatr Nephrol
, vol.10
, pp. 414-418
-
-
Wong, W.1
Hulton, S.A.2
Taylor, C.M.3
Raafat, F.4
Lote, C.J.5
Lindop, G.6
-
43
-
-
0029745589
-
An extreme example of the neonatal form of Bartter's syndrome
-
Williams MP, Jones CL, Johnstone LM, Walker RG, McCredie DA, Powell HR (1996) An extreme example of the neonatal form of Bartter's syndrome. Pediatr Nephrol 10:496-497
-
(1996)
Pediatr Nephrol
, vol.10
, pp. 496-497
-
-
Williams, M.P.1
Jones, C.L.2
Johnstone, L.M.3
Walker, R.G.4
McCredie, D.A.5
Powell, H.R.6
-
44
-
-
0027399439
-
Forme anténatale du syndrome de Bartter
-
Paris
-
Deschenes G, Burguet A, Guyot C, Hubert P, Garabedian M, Dechaux M, Loirat C, Broyer M (1993) Forme anténatale du syndrome de Bartter. Ann Pediatr (Paris) 40:95-101
-
(1993)
Ann Pediatr
, vol.40
, pp. 95-101
-
-
Deschenes, G.1
Burguet, A.2
Guyot, C.3
Hubert, P.4
Garabedian, M.5
Dechaux, M.6
Loirat, C.7
Broyer, M.8
-
45
-
-
0030045899
-
"Neonatal variant" of Bartter syndrome presenting with acidosis
-
Ammenti A, Montali S (1996) "Neonatal variant" of Bartter syndrome presenting with acidosis. Pediatr Nephrol 10:79-80
-
(1996)
Pediatr Nephrol
, vol.10
, pp. 79-80
-
-
Ammenti, A.1
Montali, S.2
-
46
-
-
0026639049
-
Case report: Familial growth hormone deficiency associated with Bartter's syndrome
-
Ruvalcaba RH, Martínez FE (1992) Case report: familial growth hormone deficiency associated with Bartter's syndrome. Am J Med Sci 303:411-414
-
(1992)
Am J Med Sci
, vol.303
, pp. 411-414
-
-
Ruvalcaba, R.H.1
Martínez, F.E.2
-
47
-
-
0025022684
-
Association of hypokalemia, aldosteronism and renal cysts
-
Torres VE, Young WF Jr, Offord KP, Hattery RR (1990) Association of hypokalemia, aldosteronism and renal cysts. N Engl J Med 322:345-351
-
(1990)
N Engl J Med
, vol.322
, pp. 345-351
-
-
Torres, V.E.1
Young Jr., W.F.2
Offord, K.P.3
Hattery, R.R.4
-
48
-
-
0017872734
-
Bartter's syndrome presenting with features resembling renal tubular acidosis. Improvement of renal tubular defects by indomethacin
-
Rodríguez-Soriano J, Vallo A, Oliveros R (1978) Bartter's syndrome presenting with features resembling renal tubular acidosis. Improvement of renal tubular defects by indomethacin. Helv Paediatr Acta 33:141-151
-
(1978)
Helv Paediatr Acta
, vol.33
, pp. 141-151
-
-
Rodríguez-Soriano, J.1
Vallo, A.2
Oliveros, R.3
-
49
-
-
0030031995
-
Vasoactive hormones and renal sclerosis
-
Egido J (1996) Vasoactive hormones and renal sclerosis. Kidney Int 49:578-597
-
(1996)
Kidney Int
, vol.49
, pp. 578-597
-
-
Egido, J.1
-
51
-
-
0028009441
-
Endothelin and vascular reactivity in Bartter's syndrome
-
Caló L, Cantaro S, Rizzolo M, Favaro S, Antonello A, Borsati A (1994) Endothelin and vascular reactivity in Bartter's syndrome. Nephron 66:370-371
-
(1994)
Nephron
, vol.66
, pp. 370-371
-
-
Caló, L.1
Cantaro, S.2
Rizzolo, M.3
Favaro, S.4
Antonello, A.5
Borsati, A.6
-
52
-
-
0017134973
-
Bartter's syndrome: A disorder characterized by high urinary prostaglandins and a dependence of hyperreninemia on prostaglandin synthesis
-
Gill JR Jr, Frölich JC, Bowden RE, Taylor AA, Keiser HR, Seyberth HW, Oates JA, Bartter FC (1976) Bartter's syndrome: a disorder characterized by high urinary prostaglandins and a dependence of hyperreninemia on prostaglandin synthesis. Am J Med 61:43-51
-
(1976)
Am J Med
, vol.61
, pp. 43-51
-
-
Gill Jr., J.R.1
Frölich, J.C.2
Bowden, R.E.3
Taylor, A.A.4
Keiser, H.R.5
Seyberth, H.W.6
Oates, J.A.7
Bartter, F.C.8
-
53
-
-
0025163142
-
Full pattern of urinary prostaglandins in Bartter's syndrome
-
Caló L, Cantaro S, Piccoli A, Favaro S, Bonfante L, Borsatti A (1990) Full pattern of urinary prostaglandins in Bartter's syndrome. Nephron 56:451-452
-
(1990)
Nephron
, vol.56
, pp. 451-452
-
-
Caló, L.1
Cantaro, S.2
Piccoli, A.3
Favaro, S.4
Bonfante, L.5
Borsatti, A.6
-
54
-
-
0017150427
-
Urinary excretion of kallikrein in Bartter's syndrome
-
Lechi A, Covi G, Lechi C, Mantero F, Scuro L (1976) Urinary excretion of kallikrein in Bartter's syndrome. J Clin Endocrinol Metab 43:1175-1178
-
(1976)
J Clin Endocrinol Metab
, vol.43
, pp. 1175-1178
-
-
Lechi, A.1
Covi, G.2
Lechi, C.3
Mantero, F.4
Scuro, L.5
-
56
-
-
0028242276
-
Long-term evolution and growth patterns in a family with Bartter's syndrome
-
Marco-Franco JE, Morey A, Ventura C, Gascó JM, Alarcón A (1994) Long-term evolution and growth patterns in a family with Bartter's syndrome. Clin Nephrol 42:33-37
-
(1994)
Clin Nephrol
, vol.42
, pp. 33-37
-
-
Marco-Franco, J.E.1
Morey, A.2
Ventura, C.3
Gascó, J.M.4
Alarcón, A.5
-
57
-
-
0027410378
-
Long-term evolution of a patient with Gitelman's syndrome
-
Betinelli A, Metta MG, Perini A, Basilico E, Santeramo C (1994) Long-term evolution of a patient with Gitelman's syndrome. Pediatr Nephrol 7:67-68
-
(1994)
Pediatr Nephrol
, vol.7
, pp. 67-68
-
-
Betinelli, A.1
Metta, M.G.2
Perini, A.3
Basilico, E.4
Santeramo, C.5
-
58
-
-
0027991625
-
Familial hypokalemia/hypomagnesemia and chondrocalcinosis
-
Smilde TJ, Haverman JF, Schipper P, Hermus AR, Lieberger FJ van, Jansen JL, Kloppenborg PW, Koolen MI (1994) Familial hypokalemia/hypomagnesemia and chondrocalcinosis. J Rheumatol 21:1515-1519
-
(1994)
J Rheumatol
, vol.21
, pp. 1515-1519
-
-
Smilde, T.J.1
Haverman, J.F.2
Schipper, P.3
Hermus, A.R.4
Van Lieberger, F.J.5
Jansen, J.L.6
Kloppenborg, P.W.7
Koolen, M.I.8
-
59
-
-
0028990162
-
2 in Gitelman's syndrome, the hypocalciuric variant of Bartter's syndrome
-
2 in Gitelman's syndrome, the hypocalciuric variant of Bartter's syndrome Am J Kidney Dis 25:824-828
-
(1995)
Am J Kidney Dis
, vol.25
, pp. 824-828
-
-
Lüthy, C.1
Betinelli, A.2
Iselin, S.3
Metta, M.G.4
Basilico, E.5
Detliker, O.H.6
Bianchetti, M.G.7
-
60
-
-
0027257174
-
Marked reduction of Tamm-Horsfall protein synthesis in hyperprostaglandin E-syndrome
-
Schröter J, Timmermans G, Seyberth HW, Greven J, Bachman S (1993) Marked reduction of Tamm-Horsfall protein synthesis in hyperprostaglandin E-syndrome. Kidney Int 44:401-410
-
(1993)
Kidney Int
, vol.44
, pp. 401-410
-
-
Schröter, J.1
Timmermans, G.2
Seyberth, H.W.3
Greven, J.4
Bachman, S.5
-
61
-
-
0016205903
-
Familial hypokalemia associated with renal interstitial fibrosis
-
Potter WZ, Trygstad CW, Helmer OM, Nance WE, Judson WE (1974) Familial hypokalemia associated with renal interstitial fibrosis. Am J Med 57:971-977
-
(1974)
Am J Med
, vol.57
, pp. 971-977
-
-
Potter, W.Z.1
Trygstad, C.W.2
Helmer, O.M.3
Nance, W.E.4
Judson, W.E.5
-
63
-
-
0028080325
-
Angiotensin II type 1 receptor gene abnormality in a patient with Bartter's syndrome
-
Yoshida H, Kakuchi J, Yoshikawa N, Saruta T, Inagami T, Phillips JA III, Ichikawa I (1994) Angiotensin II type 1 receptor gene abnormality in a patient with Bartter's syndrome. Kidney Int 46:1505-1509
-
(1994)
Kidney Int
, vol.46
, pp. 1505-1509
-
-
Yoshida, H.1
Kakuchi, J.2
Yoshikawa, N.3
Saruta, T.4
Inagami, T.5
Phillips III, J.A.6
Ichikawa, I.7
-
64
-
-
0022529728
-
Indomethacin and atrial natriuretic peptide in Bartter's syndrome
-
Gordon RD, Tunny TJ, Lemm SA (1986) Indomethacin and atrial natriuretic peptide in Bartter's syndrome. N Engl J Med 315:459
-
(1986)
N Engl J Med
, vol.315
, pp. 459
-
-
Gordon, R.D.1
Tunny, T.J.2
Lemm, S.A.3
-
65
-
-
0018747211
-
Disorders of chloriuretic hormone secretion
-
Grekin RJ, Nicholls MG, Padfield PL (1979) Disorders of chloriuretic hormone secretion. Lancet 1:1116-1118
-
(1979)
Lancet
, vol.1
, pp. 1116-1118
-
-
Grekin, R.J.1
Nicholls, M.G.2
Padfield, P.L.3
-
66
-
-
0022551792
-
Bartter's syndrome and the atrial natriuretic factor gene
-
Graham RM, Bloch KD, Delaney VB, Bourke E, Seidman JG (1986) Bartter's syndrome and the atrial natriuretic factor gene. Hypertension 8:549-551
-
(1986)
Hypertension
, vol.8
, pp. 549-551
-
-
Graham, R.M.1
Bloch, K.D.2
Delaney, V.B.3
Bourke, E.4
Seidman, J.G.5
-
67
-
-
0025358712
-
Prostaglandins regulate the synthesis and secretion of the atrial natriuretic peptide
-
Gardner DG, Schultz HD (1990) Prostaglandins regulate the synthesis and secretion of the atrial natriuretic peptide. J Clin Invest 86:52-59
-
(1990)
J Clin Invest
, vol.86
, pp. 52-59
-
-
Gardner, D.G.1
Schultz, H.D.2
-
68
-
-
0030808655
-
Salt-Iosing nephropathy associated with inappropriate secretion of atrial natriuretic peptide - A new clinical syndrome
-
Rodriguez-Soriano J, Vallo A (1997) Salt-Iosing nephropathy associated with inappropriate secretion of atrial natriuretic peptide - a new clinical syndrome. Pediatr Nephrol 11:565-572
-
(1997)
Pediatr Nephrol
, vol.11
, pp. 565-572
-
-
Rodriguez-Soriano, J.1
Vallo, A.2
-
69
-
-
0021809162
-
The pathogenic spectrum of Bartter's syndrome (1985)
-
Stein H (1985) The pathogenic spectrum of Bartter's syndrome (1985) Kidney Int 28:85-93
-
(1985)
Kidney Int
, vol.28
, pp. 85-93
-
-
Stein, H.1
-
70
-
-
0019495809
-
Prostaglandins and Bartter's syndrome
-
Dunn MJ (1981) Prostaglandins and Bartter's syndrome. Kidney Int 19:86-102
-
(1981)
Kidney Int
, vol.19
, pp. 86-102
-
-
Dunn, M.J.1
-
71
-
-
0023588270
-
Role of prostaglandins in hyperprostaglandin e syndrome and in selected renal tubular disorders
-
Seyberth HW, Koniger SJ, Rascher W, Kuhl PG, 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
-
72
-
-
0021277407
-
Hypokalemia and prostaglandin overproduction in Bartter's syndrome
-
Senba S, Konishi K, Saruta T, Ozawa Y, Kato Z, Awagasaki Y, Nakata I (1984) Hypokalemia and prostaglandin overproduction in Bartter's syndrome. Nephron 37:257-263
-
(1984)
Nephron
, vol.37
, pp. 257-263
-
-
Senba, S.1
Konishi, K.2
Saruta, T.3
Ozawa, Y.4
Kato, Z.5
Awagasaki, Y.6
Nakata, I.7
-
73
-
-
0022560274
-
Prostaglandins and other arachidonic acid metabolites in the kidney
-
Schlondorff D, Ardaillou R (1986) Prostaglandins and other arachidonic acid metabolites in the kidney. Kidney Int 28:108-119
-
(1986)
Kidney Int
, vol.28
, pp. 108-119
-
-
Schlondorff, D.1
Ardaillou, R.2
-
74
-
-
0015576864
-
Studies on the site of renal salt loss in a patient with Bartter's syndrome
-
Chaimovitz C, Levi J, Better OS, Oslander L, Benderli A (1973) Studies on the site of renal salt loss in a patient with Bartter's syndrome. Pediatr Res 7:89-94
-
(1973)
Pediatr Res
, vol.7
, pp. 89-94
-
-
Chaimovitz, C.1
Levi, J.2
Better, O.S.3
Oslander, L.4
Benderli, A.5
-
75
-
-
0016855687
-
The pathophysiology of Bartter syndrome
-
Kurtzman NA, Gutiérrez LF (1975) The pathophysiology of Bartter syndrome. JAMA 234:758-759
-
(1975)
JAMA
, vol.234
, pp. 758-759
-
-
Kurtzman, N.A.1
Gutiérrez, L.F.2
-
76
-
-
0018232460
-
Evidence for a prostaglandin-independent defect in chloride reabsorption in the loop of Henle as a proximal cause of Bartter's syndrome
-
Gill JR Jr, Bartter FC (1978) Evidence for a prostaglandin-independent defect in chloride reabsorption in the loop of Henle as a proximal cause of Bartter's syndrome. Am J Med 65.766-772
-
(1978)
Am J Med
, vol.65
, pp. 766-772
-
-
Gill Jr., J.R.1
Bartter, F.C.2
-
77
-
-
0029906224
-
The Na-(K)-Cl cotransporter family in the mammalian kidney: Molecular identification and function(s)
-
Delpire E, Kaplan MR, Plotkin MD, Hebert SC (1996) The Na-(K)-Cl cotransporter family in the mammalian kidney: molecular identification and function(s). Nephrol Dial Transplant 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
-
78
-
-
0029095609
-
An ATP-regulated, inwardly rectifying potassium channel from rat kidney (ROMK)
-
Hebert SC (1995) An ATP-regulated, inwardly rectifying potassium channel from rat kidney (ROMK). Kidney Int 48:1010-1016
-
(1995)
Kidney Int
, vol.48
, pp. 1010-1016
-
-
Hebert, S.C.1
-
80
-
-
0030357628
-
Impaired response to furosemide in hyperprostaglandin e syndrome: Evidence for a tubular defect in the loop of Henle
-
Köckerling A, Reinalter SC, Seyberth HW (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
-
-
Köckerling, A.1
Reinalter, S.C.2
Seyberth, H.W.3
-
81
-
-
0029846145
-
Arachidonic acid inhibits activity of cloned renal K+ channel, ROMK1
-
Macica CM, Yang Y, Hebert SC, Wang WH (1996) Arachidonic acid inhibits activity of cloned renal K+ channel, ROMK1. Am J Physiol 271:F588-F594
-
(1996)
Am J Physiol
, vol.271
-
-
Macica, C.M.1
Yang, Y.2
Hebert, S.C.3
Wang, W.H.4
-
82
-
-
0018656916
-
2 on chloride transport across the rabbit thick ascending limb of Henle
-
2 on chloride transport across the rabbit thick ascending limb of Henle. J Clin Invest 64:495-502
-
(1979)
J Clin Invest
, vol.64
, pp. 495-502
-
-
Stokes, J.1
-
83
-
-
0024438773
-
Hypercalciuria with Bartter's syndrome: Evidence for an abnormality of vitamin D metabolism
-
Restrepo de Rovetto C, Welch TR, Hug G, Clark KE, Bergstrom W (1989) Hypercalciuria with Bartter's syndrome: evidence for an abnormality of vitamin D metabolism. J Pediatr 115:397-404
-
(1989)
J Pediatr
, vol.115
, pp. 397-404
-
-
De Restrepo Rovetto, C.1
Welch, T.R.2
Hug, G.3
Clark, K.E.4
Bergstrom, W.5
-
85
-
-
0025200567
-
Primary structure of Torpedo marmorata chloride channel isolated by expression doming in Xenopus oocytes
-
Jentsch TJ, Steinmeyer K, Schwarz G (1990) Primary structure of Torpedo marmorata chloride channel isolated by expression doming in Xenopus oocytes. Nature 348:510-514
-
(1990)
Nature
, vol.348
, pp. 510-514
-
-
Jentsch, T.J.1
Steinmeyer, K.2
Schwarz, G.3
-
86
-
-
0028249214
-
Epithelial chloride channels, from kidney to airway cells
-
Reeves WB, Winters CJ, Zimniak K, Andreoli TE (1994) Epithelial chloride channels, from kidney to airway cells. Adv Nephrol 23:177-190
-
(1994)
Adv Nephrol
, vol.23
, pp. 177-190
-
-
Reeves, W.B.1
Winters, C.J.2
Zimniak, K.3
Andreoli, T.E.4
-
87
-
-
0030851745
-
Localization and induction by dehydration of ClC-K chloride channels in the rat kidney
-
Vanderwalle A, Cluzeaud F, Bens M, Kieferle S, Steinmeyer K, Jentsch TJ (1997) Localization and induction by dehydration of ClC-K chloride channels in the rat kidney. Am J Physiol 272:F678-F688
-
(1997)
Am J Physiol
, vol.272
-
-
Vanderwalle, A.1
Cluzeaud, F.2
Bens, M.3
Kieferle, S.4
Steinmeyer, K.5
Jentsch, T.J.6
-
88
-
-
0028360729
-
Two highly homologous members of the ClC chloride channel family in both rat and human kidney
-
Kieferle S, Fong P, Bens M, Vanderwalle A, Jentsch TJ (1994) Two highly homologous members of the ClC chloride channel family in both rat and human kidney. Proc Natl Acad Sci USA 91:6943-6947
-
(1994)
Proc Natl Acad Sci USA
, vol.91
, pp. 6943-6947
-
-
Kieferle, S.1
Fong, P.2
Bens, M.3
Vanderwalle, A.4
Jentsch, T.J.5
-
89
-
-
0343812098
-
Chloride channels: An emerging molecular picture
-
Jentsch TJ, Günther W (1996) Chloride channels: an emerging molecular picture. Bioessays 19:117-126
-
(1996)
Bioessays
, vol.19
, pp. 117-126
-
-
Jentsch, T.J.1
Günther, W.2
-
90
-
-
0019852360
-
Renal handling of water and sodium in infancy and childhood: A study using clearance methods during hypotonic saline diuresis
-
Rodríguez-Soriano J, Vallo A, Castillo G, Oliveros R (1981) Renal handling of water and sodium in infancy and childhood: a study using clearance methods during hypotonic saline diuresis. Kidney Int 20:700-704
-
(1981)
Kidney Int
, vol.20
, pp. 700-704
-
-
Rodríguez-Soriano, J.1
Vallo, A.2
Castillo, G.3
Oliveros, R.4
-
91
-
-
0023698337
-
Suppressed diluting segment reabsorption in Bartter's syndrome: Studies in 1 patient and synopsis of literature
-
Hené RJ, Koomans HA, Dorhout Mees EJ (1988) Suppressed diluting segment reabsorption in Bartter's syndrome: studies in 1 patient and synopsis of literature. Am J Nephrol 8:402-409
-
(1988)
Am J Nephrol
, vol.8
, pp. 402-409
-
-
Hené, R.J.1
Koomans, H.A.2
Dorhout Mees, E.J.3
-
92
-
-
0022971409
-
Renal tubular reabsorption of chloride in Bartter's syndrome and other conditions with hypokalemia
-
Rodríguez Portales JA, Delea CS (1986) Renal tubular reabsorption of chloride in Bartter's syndrome and other conditions with hypokalemia. Clin Nephrol 6:269-272
-
(1986)
Clin Nephrol
, vol.6
, pp. 269-272
-
-
Rodríguez Portales, J.A.1
Delea, C.S.2
-
93
-
-
0028441278
-
Comparative study of two tests of renal diluting ability in Bartter's syndrome
-
Ferreira SR, Kater CE (1994) Comparative study of two tests of renal diluting ability in Bartter's syndrome. Braz J Med Biol Res 27:1181-1191
-
(1994)
Braz J Med Biol Res
, vol.27
, pp. 1181-1191
-
-
Ferreira, S.R.1
Kater, C.E.2
-
95
-
-
0026843448
-
Heterogenous derangement of cellular sodium metabolism in Bartter's syndrome. Description of two cases and review of the literature
-
Sechi LA, Melis A, Faedda R, Tedde R, Bartoli E (1992) Heterogenous derangement of cellular sodium metabolism in Bartter's syndrome. Description of two cases and review of the literature. Panminerva Med 34:85-92
-
(1992)
Panminerva Med
, vol.34
, pp. 85-92
-
-
Sechi, L.A.1
Melis, A.2
Faedda, R.3
Tedde, R.4
Bartoli, E.5
-
96
-
-
0021707149
-
Correction of hypokalemia corrects the abnormalities in erythrocyte sodium transport in Bartter's syndrome
-
Korff JM, Siebens AW, Gill JR Jr (1984) Correction of hypokalemia corrects the abnormalities in erythrocyte sodium transport in Bartter's syndrome. J Clin Invest 74:1724-1729
-
(1984)
J Clin Invest
, vol.74
, pp. 1724-1729
-
-
Korff, J.M.1
Siebens, A.W.2
Gill Jr., J.R.3
-
97
-
-
0029148777
-
Renal tubular function in children and adolescents with Gitelman's syndrome, the hypocalciuric variant of Bartter's syndrome
-
Peters N, Betinelli A, Spicher I, Basilico E, Metta MG, Bianchetti MG (1995) Renal tubular function in children and adolescents with Gitelman's syndrome, the hypocalciuric variant of Bartter's syndrome. Neprol Dial Transplant 10:1313-1319
-
(1995)
Neprol Dial Transplant
, vol.10
, pp. 1313-1319
-
-
Peters, N.1
Betinelli, A.2
Spicher, I.3
Basilico, E.4
Metta, M.G.5
Bianchetti, M.G.6
-
98
-
-
0026738926
-
Familial hypokalemia-hypomagnesemia or Gitelman's syndrome: A further case
-
Zárraga Larrondo S, Vallo A, Gainza J, Muñoz R, García Erauzkin G, Lampreabe I (1992) Familial hypokalemia-hypomagnesemia or Gitelman's syndrome: a further case. Nephron 62:340-344
-
(1992)
Nephron
, vol.62
, pp. 340-344
-
-
Zárraga Larrondo, S.1
Vallo, A.2
Gainza, J.3
Muñoz, R.4
García Erauzkin, G.5
Lampreabe, I.6
-
99
-
-
0021992371
-
Bartter's syndrome due to a defect in salt reabsorption in the distal convoluted tubule
-
Uribarri J, Alveranga D, Oh MS, Kukar NM, Del Monte ML, Carroll HJ (1985) Bartter's syndrome due to a defect in salt reabsorption in the distal convoluted tubule. Nephron 40:52-56
-
(1985)
Nephron
, vol.40
, pp. 52-56
-
-
Uribarri, J.1
Alveranga, D.2
Oh, M.S.3
Kukar, N.M.4
Del Monte, M.L.5
Carroll, H.J.6
-
100
-
-
0023680022
-
Variant of Bartter's syndrome with distal tubular rather than loop of Henle defect
-
Puschett JB, Greenberg A, Mitro T, Piraino B, Wallia R (1988) Variant of Bartter's syndrome with 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, T.3
Piraino, B.4
Wallia, R.5
-
101
-
-
0023695862
-
Bartter's syndrome with a salt reabsorption defect in the cortical part of Henle's loop
-
Soupart A, Unger J, Debieve MF, Decaux G (1988) Bartter's syndrome with a salt reabsorption defect in the cortical part of Henle's loop. Am J Nephrol 8:309-315
-
(1988)
Am J Nephrol
, vol.8
, pp. 309-315
-
-
Soupart, A.1
Unger, J.2
Debieve, M.F.3
Decaux, G.4
-
102
-
-
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 (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
-
-
Ral, S.1
Mavichak, V.2
Halabe, A.3
Wilkins, G.E.4
-
103
-
-
0030975973
-
- by the thiazide-inhibitable transporter of the distal convoluted tubule in Gitelman's syndrome
-
- by the thiazide-inhibitable transporter of the distal convoluted tubule in Gitelman's syndrome. Am J Nephrol 17:103-111
-
(1997)
Am J Nephrol
, vol.17
, pp. 103-111
-
-
Colussi, G.1
Romboli, G.2
Brunati, C.3
De Ferrari, M.E.4
-
104
-
-
0025153324
-
Familial hypokalemia-hypomagnesemia (Gitelman's syndrome)
-
Rodríguez-Soriano J, Vallo A (1990) Familial hypokalemia-hypomagnesemia (Gitelman's syndrome). Pcdiatr Nephrol 4:C22
-
(1990)
Pcdiatr Nephrol
, vol.4
-
-
Rodríguez-Soriano, J.1
Vallo, A.2
-
106
-
-
0028851318
-
Evidence for disturbed regulation of calciotropic hormone metabolism in Gitelman syndrome
-
Bianchetti MG, Betinelli A, Casez JP, Basilico E, Metta MG, Spicher I, Santeramo C, Bigoni M, Jaeger PH (1995) Evidence for disturbed regulation of calciotropic hormone metabolism in Gitelman syndrome. J Clin Endocrinol Metab 80:224-228
-
(1995)
J Clin Endocrinol Metab
, vol.80
, pp. 224-228
-
-
Bianchetti, M.G.1
Betinelli, A.2
Casez, J.P.3
Basilico, E.4
Metta, M.G.5
Spicher, I.6
Santeramo, C.7
Bigoni, M.8
Jaeger, P.H.9
-
107
-
-
0030707887
-
Renal magnesium handling: New perspectives in understanding old problems
-
Quamme GA (1997) Renal magnesium handling: new perspectives in understanding old problems. Kidney Int 52:1180-1195
-
(1997)
Kidney Int
, vol.52
, pp. 1180-1195
-
-
Quamme, G.A.1
-
109
-
-
0028220576
-
Renal magnesium handling and its hormonal control
-
De Rouffignac C, Quamme G (1994) Renal magnesium handling and its hormonal control. Physiol Rev 74:105-322
-
(1994)
Physiol Rev
, vol.74
, pp. 105-322
-
-
De Rouffignac, C.1
Quamme, G.2
-
110
-
-
0029979549
-
Severe hyperchloriduria-hyperkaliuria: A new congenital renal tubular abnormality ?
-
Meyburg J, Mayatepek E, Huffman GF, Linderkamp O, Seyberth HW (1996) Severe hyperchloriduria-hyperkaliuria: a new congenital renal tubular abnormality ? J Pediatr 128:376-378
-
(1996)
J Pediatr
, vol.128
, pp. 376-378
-
-
Meyburg, J.1
Mayatepek, E.2
Huffman, G.F.3
Linderkamp, O.4
Seyberth, H.W.5
-
111
-
-
0026500865
-
Pseudohypoaldosteronism in a preterm infant: Intrauterine presentation as hydramnios
-
Abraham O, Zmora E, Mazor M, Shinwell ES (1992) Pseudohypoaldosteronism in a preterm infant: intrauterine presentation as hydramnios. J Pediatr 120:129-132
-
(1992)
J Pediatr
, vol.120
, pp. 129-132
-
-
Abraham, O.1
Zmora, E.2
Mazor, M.3
Shinwell, E.S.4
-
112
-
-
0029000690
-
Fetal pseudohypoaldosteronism: Another cause of hydramnios
-
Greenberg D, Abramson O, Phillip M (1995) Fetal pseudohypoaldosteronism: another cause of hydramnios. Acta Paediatr 84:582-584
-
(1995)
Acta Paediatr
, vol.84
, pp. 582-584
-
-
Greenberg, D.1
Abramson, O.2
Phillip, M.3
-
113
-
-
0028105932
-
Nephrocalcinosis in pseudohypoaldosteronism and the effect of indomethacin therapy
-
Shalev H, Ohali M, Abramson O, Phillip M (1994) Nephrocalcinosis in pseudohypoaldosteronism and the effect of indomethacin therapy. J Pediatr 125:246-248
-
(1994)
J Pediatr
, vol.125
, pp. 246-248
-
-
Shalev, H.1
Ohali, M.2
Abramson, O.3
Phillip, M.4
-
114
-
-
0029785283
-
Effect of hydrochlorothiazide in pseudohypoaldosteronism with hypercalciuria and severe hyperkalemia
-
Stone RC, Vale P, Rosa FC (1996) Effect of hydrochlorothiazide in pseudohypoaldosteronism with hypercalciuria and severe hyperkalemia. Pediatr Nephrol 10: 501-503
-
(1996)
Pediatr Nephrol
, vol.10
, pp. 501-503
-
-
Stone, R.C.1
Vale, P.2
Rosa, F.C.3
-
115
-
-
0024789685
-
Exogenous prostaglandin administration and pseudo-Bartter syndrome
-
Langhendries JP, Thiry V, Bodart E, Delfosse G, Whitofs L, Battisti O, Bertrand JM (1989) Exogenous prostaglandin administration and pseudo-Bartter syndrome. Eur J Pediatr 149: 208-209
-
(1989)
Eur J Pediatr
, vol.149
, pp. 208-209
-
-
Langhendries, J.P.1
Thiry, V.2
Bodart, E.3
Delfosse, G.4
Whitofs, L.5
Battisti, O.6
Bertrand, J.M.7
-
116
-
-
0016692788
-
Un syndrome de Bartter associant un hypercortisolisme, un diabète phosphoré et magnésien et une tubulopathie d'origine familiale
-
Sann L, Moreau P, Longin B, Sassard J, François R (1975) Un syndrome de Bartter associant un hypercortisolisme, un diabète phosphoré et magnésien et une tubulopathie d'origine familiale. Arch Fr Pediatr 32:349-366
-
(1975)
Arch Fr Pediatr
, vol.32
, pp. 349-366
-
-
Sann, L.1
Moreau, P.2
Longin, B.3
Sassard, J.4
François, R.5
-
117
-
-
0018637391
-
Bartter's syndrome: 10 cases in childhood. Results of long-term indometancin therapy
-
Dillon MJ, Shah V, Mitchell MD (1979) Bartter's syndrome: 10 cases in childhood. Results of long-term indometancin therapy. Q J Med 48.429-446
-
(1979)
Q J Med
, vol.48
, pp. 429-446
-
-
Dillon, M.J.1
Shah, V.2
Mitchell, M.D.3
-
119
-
-
0018653582
-
A familial disorder with hypokalemic alkalosis, hyperreninemia, aldosteronism, high urinary prostaglandins and normal blood pressure that is not "Bartter's syndrome."
-
Güllner MG, Gill JR Jr, Bartter FC,Chan JCM, Dickman PS (1979) A familial disorder with hypokalemic alkalosis, hyperreninemia, aldosteronism, high urinary prostaglandins and normal blood pressure that is not "Bartter's syndrome." Trans Assoc Am Physicians 92:175-188
-
(1979)
Trans Assoc Am Physicians
, vol.92
, pp. 175-188
-
-
Güllner, M.G.1
Gill Jr., J.R.2
Bartter, F.C.3
Chan, J.C.M.4
Dickman, P.S.5
-
120
-
-
84948725536
-
A sibship with hypokalemic alkalosis and renal proximal tubulopathy
-
Güllner HG, Bartter FC, Gill JR Jr, Dickman PS, Wilson CB, Tiwari JL (1983) A sibship with hypokalemic alkalosis and renal proximal tubulopathy. Arch Intern Med 143:1534-1540
-
(1983)
Arch Intern Med
, vol.143
, pp. 1534-1540
-
-
Güllner, H.G.1
Bartter, F.C.2
Gill Jr., J.R.3
Dickman, P.S.4
Wilson, C.B.5
Tiwari, J.L.6
-
121
-
-
0014271407
-
Fanconi syndrome with renal sodium wasting and metabolic alkalosis
-
Houston IB, Boichis H, Edelmann CM Jr (1968) Fanconi syndrome with renal sodium wasting and metabolic alkalosis. Am J Med 44:638-646
-
(1968)
Am J Med
, vol.44
, pp. 638-646
-
-
Houston, I.B.1
Boichis, H.2
Edelmann Jr., C.M.3
-
122
-
-
0019190843
-
A patient with cystinosis presenting with the features of Bartter syndrome
-
O'Regan S, Mongeau JG, Robitaille P (1980) A patient with cystinosis presenting with the features of Bartter syndrome. Acta Paediatr Belg 33:51-52
-
(1980)
Acta Paediatr Belg
, vol.33
, pp. 51-52
-
-
O'Regan, S.1
Mongeau, J.G.2
Robitaille, P.3
-
123
-
-
0022005318
-
Cystinosis with features suggesting Bartter's syndrome
-
Phila
-
Whyte P, Shaheb S, Schnaper HW (1985) Cystinosis with features suggesting Bartter's syndrome. Clin Pediatr (Phila) 24: 447-451
-
(1985)
Clin Pediatr
, vol.24
, pp. 447-451
-
-
Whyte, P.1
Shaheb, S.2
Schnaper, H.W.3
-
124
-
-
0025314193
-
Renal tubular involvement mimicking Bartter syndrome in a patient with Kearns-Sayre syndrome
-
Goto Y, Itami N, Kajii N, Tochimaru H, Endo M, Horai S (1990) Renal tubular involvement mimicking Bartter syndrome in a patient with Kearns-Sayre syndrome. J Pediatr 116:904-910
-
(1990)
J Pediatr
, vol.116
, pp. 904-910
-
-
Goto, Y.1
Itami, N.2
Kajii, N.3
Tochimaru, H.4
Endo, M.5
Horai, S.6
-
125
-
-
85047696296
-
Pseudo-Bartter's syndrome from surreptitious diuretic intake: Differential diagnosis with true Bartter's syndrome
-
Colussi G, Rambolá G, Airaghi C, De Ferrari ME, Minetti L (1992) Pseudo-Bartter's syndrome from surreptitious diuretic intake: differential diagnosis with true Bartter's syndrome. Nephrol Dial Transplant 7:896-901
-
(1992)
Nephrol Dial Transplant
, vol.7
, pp. 896-901
-
-
Colussi, G.1
Rambolá, G.2
Airaghi, C.3
De Ferrari, M.E.4
Minetti, L.5
-
126
-
-
0031034785
-
Hypokalemic metabolic alkalosis with hypomagnesuric hypermagnesemia and severe hypocalciuria: A new syndrome?
-
Mehrotra R, Nolph KD, Kathuria P, Dotson L (1997) Hypokalemic metabolic alkalosis with hypomagnesuric hypermagnesemia and severe hypocalciuria: a new syndrome? Am J Kidney Dis 29:106-114
-
(1997)
Am J Kidney Dis
, vol.29
, pp. 106-114
-
-
Mehrotra, R.1
Nolph, K.D.2
Kathuria, P.3
Dotson, L.4
-
127
-
-
0023182432
-
Correction of hypokalemia in Bartter's syndrome by enalapril
-
Hené RJ, Koomans HA, Dorhout Mees EJ, Stolpe A, Verhoef GEG, Boer P (1987) Correction of hypokalemia in Bartter's syndrome by enalapril Am J Kidney Dis 9:200-205
-
(1987)
Am J Kidney Dis
, vol.9
, pp. 200-205
-
-
Hené, R.J.1
Koomans, H.A.2
Dorhout Mees, E.J.3
Stolpe, A.4
Geg, V.5
Boer, P.6
-
128
-
-
0025346695
-
Captopril treatment in Bartter's syndrome
-
Scherling B, Verder H, Nielsen MSD, Christensen P, Giese J (1990) Captopril treatment in Bartter's syndrome. Scand J Urol Nephrol 214:123-125
-
(1990)
Scand J Urol Nephrol
, vol.214
, pp. 123-125
-
-
Scherling, B.1
Verder, H.2
Nielsen, M.S.D.3
Christensen, P.4
Giese, J.5
-
129
-
-
0029160208
-
Anaesthetic management of a child with Bartter's syndrome
-
Kannan S, Delph Y, Moseley HS (1995) Anaesthetic management of a child with Bartter's syndrome. Can J Anaesth 42: 808-812
-
(1995)
Can J Anaesth
, vol.42
, pp. 808-812
-
-
Kannan, S.1
Delph, Y.2
Moseley, H.S.3
-
130
-
-
0028356071
-
Correction of hypokalemia with antialdosterone therapy in Gitelman's syndrome
-
Colussi G, Rombolà G, De Ferrari ME, Macaluso M, Minetti L (1994) Correction of hypokalemia with antialdosterone therapy in Gitelman's syndrome Am J Nephrol 14:127-135
-
(1994)
Am J Nephrol
, vol.14
, pp. 127-135
-
-
Colussi, G.1
Rombolà, G.2
De Ferrari, M.E.3
Macaluso, M.4
Minetti, L.5
|