-
1
-
-
0031779521
-
Bartter and related syndromes. The puzzle is almost solved
-
Rodriguez-Soriano J (1998) Bartter and related syndromes. The puzzle is almost solved. Pediatr Nephrol 12:315-327
-
(1998)
Pediatr. Nephrol.
, vol.12
, pp. 315-327
-
-
Rodriguez-Soriano, J.1
-
2
-
-
0032144244
-
Bartter syndrome: Unraveling the pathophysiologic enigma
-
Guay-Woodford LM (1998) Bartter syndrome: unraveling the pathophysiologic enigma. Am J Med 105:151-161
-
(1998)
Am. J. Med.
, vol.105
, pp. 151-161
-
-
Guay-Woodford, L.M.1
-
3
-
-
0041382927
-
Hypokalemic salt-losing tubulopathies: An evolving story
-
Zelikovic I (2003) Hypokalemic salt-losing tubulopathies: an evolving story. Nephrol Dial Transplant 18:1696-1700
-
(2003)
Nephrol. Dial. Transplant.
, vol.18
, pp. 1696-1700
-
-
Zelikovic, I.1
-
4
-
-
0037082531
-
Clinical presentation of genetically defined patients with hypokalemic salt-losing tubulopathies
-
Peters M, Jeck N, Reinalter S, Leonhardt A, Tönshoff B, Klaus G, Konrad M, Seyberth H (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
Leonhardt, A.4
Tönshoff, B.5
Klaus, G.6
Konrad, M.7
Seyberth, H.8
-
5
-
-
0017803065
-
Treatment of Bartter's syndrome in early childhood with prostaglandin synthetase inhibitors
-
Littlewood JM, Lee MR, Meadow SR (1978) Treatment of Bartter's syndrome in early childhood with prostaglandin synthetase inhibitors. Arch Dis Child 53:43-48
-
(1978)
Arch. Dis. Child
, vol.53
, pp. 43-48
-
-
Littlewood, J.M.1
Lee, M.R.2
Meadow, S.R.3
-
6
-
-
0042839701
-
The neonatal variant of Bartter syndrome and deafness: Preservation of renal function
-
Shalev H, Ohali M, Kachko L, Landau D (2003) The neonatal variant of Bartter syndrome and deafness: preservation of renal function. Pediatrics 112:628-633
-
(2003)
Pediatrics
, vol.112
, pp. 628-633
-
-
Shalev, H.1
Ohali, M.2
Kachko, L.3
Landau, D.4
-
7
-
-
0038148126
-
Successful management of an extreme example of neonatal hyperprostaglandin-E syndrome (Bartter's syndrome) with the new cyclooxygenase-2 inhibitor rofecoxib
-
Haas NA, Nossal R, Schneider CH, Lewin MAG, Ocker V, Holder M, Uhlemann F (2003) Successful management of an extreme example of neonatal hyperprostaglandin-E syndrome (Bartter's syndrome) with the new cyclooxygenase-2 inhibitor rofecoxib. Pediatr Crit Care Med 4:249-251
-
(2003)
Pediatr. Crit. Care Med.
, vol.4
, pp. 249-251
-
-
Haas, N.A.1
Nossal, R.2
Schneider, C.H.3
Lewin, M.A.G.4
Ocker, V.5
Holder, M.6
Uhlemann, F.7
-
8
-
-
0034968357
-
Genotype/phenotype observations in African Americans with Bartter syndrome
-
Schurman S, Perlman AS, Sertphen R, Campos A, Garin E, Cruz D, Schoemaker L (2001) Genotype/phenotype observations in African Americans with Bartter syndrome. J Pediatr 139:105-110
-
(2001)
J. Pediatr.
, vol.139
, pp. 105-110
-
-
Schurman, S.1
Perlman, A.S.2
Sertphen, R.3
Campos, A.4
Garin, E.5
Cruz, D.6
Schoemaker, L.7
-
9
-
-
0023182432
-
Correction of hypokalemia in Bartter's syndrome by enalapril
-
Hene RJ, Koomans HÁ, Dorhout Mees EJ, Stople 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
-
-
Hene, R.J.1
Koomans, H.Á.2
Dorhout Mees, E.J.3
Stople, A.4
Verhoef, G.E.G.5
Boer, P.6
-
10
-
-
0012571971
-
Steady-state plasma concentrations of rofecoxib in children (ages 2-5 years) with juvenile rheumatoid arthritis (JRA)
-
St Rose E, Ferrandiz M, Kiss M, Forre O, Vehe R, Higgins G, Rennenbohm R, Porras A, Wong P, DeTora LM, Truitt KE (2001) Steady-state plasma concentrations of rofecoxib in children (ages 2-5 years) with juvenile rheumatoid arthritis (JRA). Arthritis Rheum 44:S291
-
(2001)
Arthritis Rheum.
, vol.44
-
-
St Rose, E.1
Ferrandiz, M.2
Kiss, M.3
Forre, O.4
Vehe, R.5
Higgins, G.6
Rennenbohm, R.7
Porras, A.8
Wong, P.9
DeTora, L.M.10
Truitt, K.E.11
-
11
-
-
0036318596
-
Role of cyclooxigenase-2 in hyperprostaglandin E syndrome/antenatal Bartter symdrome
-
Reinalter SC, Jeck N, Brochhausen C, Watzer B, Nüsing RM, Seyberth HW, Kömhoff M (2002) Role of cyclooxigenase-2 in hyperprostaglandin E syndrome/antenatal Bartter symdrome. Kidney Int 62:253-260
-
(2002)
Kidney Int.
, vol.62
, pp. 253-260
-
-
Reinalter, S.C.1
Jeck, N.2
Brochhausen, C.3
Watzer, B.4
Nüsing, R.M.5
Seyberth, H.W.6
Kömhoff, M.7
-
12
-
-
0023179130
-
The use of plasma creatinine and urea concentration for estimating glomerular filtration rate in infants, children and adolescents
-
Schwartz GJ, Brion LP, Spitzer A (1987) The use of plasma creatinine and urea concentration for estimating glomerular filtration rate in infants, children and adolescents. Pediatr Clin North Am 34:571-590
-
(1987)
Pediatr. Clin. North Am.
, vol.34
, pp. 571-590
-
-
Schwartz, G.J.1
Brion, L.P.2
Spitzer, A.3
-
13
-
-
0030032699
-
Bartter's syndrome, hypokalemic alkalosis with hypercalciuria, is caused by mutations in the Na-K-2Cl, cotransporter NKCC2
-
Simon DB, Karet FE, Hamdan JM, DiPietro A, Sanjad AS, Lifton RP (1996) Bartter's syndrome, hypokalemic 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
DiPietro, A.4
Sanjad, A.S.5
Lifton, R.P.6
-
14
-
-
0029794875
-
Genetic heterogeneity of Bartter's syndrome revealed by mutations in the K+ channel, ROMK
-
Simon DB, Karet FE, Rodriguez-Soriano J, Hamdan JH, DiPietro A, Trachtman H, Sanjad AS, Lifton RP (1996) 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.B.1
Karet, F.E.2
Rodriguez-Soriano, J.3
Hamdan, J.H.4
DiPietro, A.5
Trachtman, H.6
Sanjad, A.S.7
Lifton, R.P.8
-
15
-
-
16944366243
-
Mutations in the chloride channel ClC-Kb cause Bartter's syndrome type III
-
Simon DB, Bindra RS, Mansfield TA, Nelson-Willians C, Mendonca E, Stone R, Schurman S, Nayir A, Alpay H, Bakkaloglu A, Rodriguez-Soriano J, Morales JM, Sanjad AS, 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
Mansfield, T.A.3
Nelson-Willians, C.4
Mendonca, E.5
Stone, R.6
Schurman, S.7
Nayir, A.8
Alpay, H.9
Bakkaloglu, A.10
Rodriguez-Soriano, J.11
Morales, J.M.12
Sanjad, A.S.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..
-
16
-
-
9044235777
-
Gitelman's variant of Bartter's syndrome, inherited hypokalemic alkalosis, is caused by mutations in the thiazide-sensitive Na-Cl cotransporter
-
Simon DB, Nelson-Willians C, Bia MJ, Ellison D, Karet FE, Molina AM, Vaara I, Iwata F, Cushner HM, Koolen M, Gainza FJ, Gitleman HJ, Lifton RP (1996) Gitelman's variant of Bartter's syndrome, inherited hypokalemic 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-Willians, C.2
Bia, M.J.3
Ellison, D.4
Karet, F.E.5
Molina, A.M.6
Vaara, I.7
Iwata, F.8
Cushner, H.M.9
Koolen, M.10
Gainza, F.J.11
Gitleman, H.J.12
Lifton, R.P.13
-
17
-
-
0035408815
-
Hypokalemic salt-losing tubulopathy with chronic renal failure and sensorineural deafness
-
Jeck N, Reinalter SC, Henne T, Marg W, Mallman R, Pasel K, Vollner M, Klaus G, Leonhardt A, Seyberth H, Konrad M (2001) Hypokalemic salt-losing tubulopathy with chronic renal failure and sensorineural deafness. Pediatrics 108:1-9
-
(2001)
Pediatrics
, vol.108
, pp. 1-9
-
-
Jeck, N.1
Reinalter, S.C.2
Henne, T.3
Marg, W.4
Mallman, R.5
Pasel, K.6
Vollner, M.7
Klaus, G.8
Leonhardt, A.9
Seyberth, H.10
Konrad, M.11
-
18
-
-
0036707879
-
Functional characterization of a calcium-sensing receptor mutation in severe autosomal dominant hypocalcemia with a Bartter-like syndrome
-
Vargas-Poussou R, Huang C, Hulin P, Houillier P, Jeunemaitre X, Paillard M, Planelles G, Déchaux M, Miller RT, Antignac C (2002) Functional characterization of a calcium-sensing receptor mutation in severe autosomal dominant hypocalcemia with a Bartter-like syndrome. J Am Soc Nephrol 13:2259-2266
-
(2002)
J. Am. Soc. Nephrol.
, vol.13
, pp. 2259-2266
-
-
Vargas-Poussou, R.1
Huang, C.2
Hulin, P.3
Houillier, P.4
Jeunemaitre, X.5
Paillard, M.6
Planelles, G.7
Déchaux, M.8
Miller, R.T.9
Antignac, C.10
-
19
-
-
0037206034
-
Association between activating mutations of calcium-sensing receptor and Bartter's syndrome
-
Watanabe S, Fukumoto S, Chang H, Takeuchi Y, Hasegawa Y, Okazaki R, Chikatsu N, Fujita T (2002) Association between activating mutations of calcium-sensing receptor and Bartter's syndrome. Lancet 360:692-694
-
(2002)
Lancet
, vol.360
, pp. 692-694
-
-
Watanabe, S.1
Fukumoto, S.2
Chang, H.3
Takeuchi, Y.4
Hasegawa, Y.5
Okazaki, R.6
Chikatsu, N.7
Fujita, T.8
-
20
-
-
0023765041
-
Bartter's syndrome. A review of 28 patients followed for 10 years
-
Rudin A (1988) Bartter's syndrome. A review of 28 patients followed for 10 years. Acta Med Scand 224:165-171
-
(1988)
Acta Med. Scand.
, vol.224
, pp. 165-171
-
-
Rudin, A.1
-
21
-
-
0018637391
-
Bartter's syndrome: Ten cases in childhood
-
Dillon MJ, Shah V, Mitchell MD (1979) Bartter's syndrome: ten cases in childhood. 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
-
22
-
-
0029150626
-
A patient with chronic renal failure due to Bartter's syndrome
-
Sato K, Ogata M (1995) A patient with chronic renal failure due to Bartter's syndrome. Nippon Jinzo Shi 37:404-409
-
(1995)
Nippon Jinzo Shi
, vol.37
, pp. 404-409
-
-
Sato, K.1
Ogata, M.2
-
23
-
-
0028327671
-
Risk of upper gastrointestinal bleeding and perforation associated with individual non-steroidal anti-inflammatory drugs
-
Rodriguez LAG, Jick H (1994) Risk of upper gastrointestinal bleeding and perforation associated with individual non-steroidal anti-inflammatory drugs. Lancet 343:769-772
-
(1994)
Lancet
, vol.343
, pp. 769-772
-
-
Rodriguez, L.A.G.1
Jick, H.2
-
24
-
-
4344647270
-
Gastrocolic fistulae in Bartter's syndrome caused by indomethacin: Report of two cases
-
Barbosa PR, Abe JM, Oliveira LAN, Vaisbich MH, Koch VHK, Cerri GG (2003) Gastrocolic fistulae in Bartter's syndrome caused by indomethacin: report of two cases. Radiol Bras 36:179-181
-
(2003)
Radiol. Bras.
, vol.36
, pp. 179-181
-
-
Barbosa, P.R.1
Abe, J.M.2
Oliveira, L.A.N.3
Vaisbich, M.H.4
Koch, V.H.K.5
Cerri, G.G.6
|