-
1
-
-
0030918271
-
Bartter syndrome in Costa Rica: A description of 20 cases
-
Madrigal G, Saborio P, Mora F, et al: Bartter syndrome in Costa Rica: A description of 20 cases. Pediatr Nephrol 1997; 11:296-301
-
(1997)
Pediatr Nephrol
, vol.11
, pp. 296-301
-
-
Madrigal, G.1
Saborio, P.2
Mora, F.3
-
3
-
-
0033661429
-
The diuretic- and Bartter-like salt-losing tubulopathies
-
Jeck N, Konrad M, Hess M, et al: The diuretic- and Bartter-like salt-losing tubulopathies. Nephrol Dial Transplant 2000; 15
-
(2000)
Nephrol Dial Transplant
, vol.15
-
-
Jeck, N.1
Konrad, M.2
Hess, M.3
-
4
-
-
0035033166
-
Ion channel in disease
-
Bockenhauer D: Ion channel in disease. Curr Opin Pediatr 2001; 13:142-149
-
(2001)
Curr Opin Pediatr
, vol.13
, pp. 142-149
-
-
Bockenhauer, D.1
-
5
-
-
0029794875
-
Genetic heterogeneity of Bartter's syndrome revealed by mutations in the K- channel
-
Simon DB, Karet FE, Rodriguez-Soriano J, et al: Genetic heterogeneity of Bartter's syndrome revealed by mutations in the K- channel, ROMK. Nat Genet 1996; 14:152-156
-
(1996)
ROMK. Nat Genet
, vol.14
, pp. 152-156
-
-
Simon, D.B.1
Karet, F.E.2
Rodriguez-Soriano, J.3
-
6
-
-
0029778992
-
Gitelman's syndrome is genetically distinct from other forms of Bartter's syndrome
-
Károlyi L, Ziegler A, Pollak M, et al: Gitelman's syndrome is genetically distinct from other forms of Bartter's syndrome. Pediatr Nephrol 1996; 10:551-554
-
(1996)
Pediatr Nephrol
, vol.10
, pp. 551-554
-
-
Károlyi, L.1
Ziegler, A.2
Pollak, M.3
-
7
-
-
0029951224
-
The molecular basis of inherited hypokalemic alkalosis: Bartter's and Gitelman's syndromes
-
Simon DB, Lifton RP: The molecular basis of inherited hypokalemic alkalosis: Bartter's and Gitelman's syndromes. Am J Physiol 1996; 271:F961-F966
-
(1996)
Am J Physiol
, vol.271
-
-
Simon, D.B.1
Lifton, R.P.2
-
8
-
-
0033914432
-
Mutations in the chloride channel gene CLCNKB as a cause of classic Bartter syndrome
-
Konrad M, Vollmer M, Lemmink H, et al: Mutations in the chloride channel gene CLCNKB as a cause of classic Bartter syndrome. J Am Soc Nephrol 2000; 11:1449-1459
-
(2000)
J Am Soc Nephrol
, vol.11
, pp. 1449-1459
-
-
Konrad, M.1
Vollmer, M.2
Lemmink, H.3
-
10
-
-
0030954698
-
Bartter syndrome and its neonatal variant
-
Proesmans W: Bartter syndrome and its neonatal variant. Eur J Pediatr 1997; 156:669-679
-
(1997)
Eur J Pediatr
, vol.156
, pp. 669-679
-
-
Proesmans, W.1
-
11
-
-
0031779521
-
Bartter and related syndromes: The puzzle is almost solved
-
Rodriguez-Soriano J: Bartter and related syndromes: The puzzle is almost solved. Pediatr Nephrol 1998:315-327
-
(1998)
Pediatr Nephrol
, pp. 315-327
-
-
Rodriguez-Soriano, J.1
-
12
-
-
0029745589
-
An extreme example of the neonatal form of Bartter's syndrome
-
Williams MP, Jones CL, Johnstone LM, et al: An extreme example of the neonatal form of Bartter's syndrome. Pediatr Nephrol 1996; 10:496-497
-
(1996)
Pediatr Nephrol
, vol.10
, pp. 496-497
-
-
Williams, M.P.1
Jones, C.L.2
Johnstone, L.M.3
-
14
-
-
17344392679
-
Prenatal and postnatal management of hyperprostaglandin e syndrome after genetic diagnosis from amniocytes
-
Konrad M, Leonhardt A, Hensen P, et al: Prenatal and postnatal management of hyperprostaglandin E syndrome after genetic diagnosis from amniocytes. Pediatrics 1999; 103: 678-683
-
(1999)
Pediatrics
, vol.103
, pp. 678-683
-
-
Konrad, M.1
Leonhardt, A.2
Hensen, P.3
-
15
-
-
0033672190
-
Cyclooxygenase-2 expression is associated with the renal macula densa of patients with Bartter-like syndrome
-
Komhoff M, Jeck ND, Seyberth WW, et al: Cyclooxygenase-2 expression is associated with the renal macula densa of patients with Bartter-like syndrome. Kidney Int 2000; 58: 2420-2424
-
(2000)
Kidney Int
, vol.58
, pp. 2420-2424
-
-
Komhoff, M.1
Jeck, N.D.2
Seyberth, W.W.3
-
16
-
-
13344287064
-
Indomethacin for renal impairment in neonatal Bartter's syndrome
-
Craig JC, Falk MC: Indomethacin for renal impairment in neonatal Bartter's syndrome. Lancet 1996; 347:550
-
(1996)
Lancet
, vol.347
, pp. 550
-
-
Craig, J.C.1
Falk, M.C.2
-
17
-
-
0029803436
-
Neonatal Bartter's syndrome: Use of indomethacin in the newborn period and prevention of growth failure
-
Mackie FE, Hodson EM, Roy LP, et al: Neonatal Bartter's syndrome: Use of indomethacin in the newborn period and prevention of growth failure. Pediatr Nephrol 1996; 10:756-758
-
(1996)
Pediatr Nephrol
, vol.10
, pp. 756-758
-
-
Mackie, F.E.1
Hodson, E.M.2
Roy, L.P.3
-
18
-
-
0023916322
-
Growth from birth to adulthood in a patient with the neonatal form of Bartter syndrome
-
Proesmans W, Massa G, Vanderschueren- Lodeweyckx M: Growth from birth to adulthood in a patient with the neonatal form of Bartter syndrome. Pediatr Nephrol 1988; 2:205-209
-
(1988)
Pediatr Nephrol
, vol.2
, pp. 205-209
-
-
Proesmans, W.1
Massa, G.2
Vanderschueren-Lodeweyckx, M.3
-
19
-
-
0033962623
-
Bartter syndrome in a neonate: Early treatment with indomethacin
-
Mourani CC, Sanjad SA, Akatcherian CY: Bartter syndrome in a neonate: Early treatment with indomethacin. Pediatr Nephrol 2000; 14:143-145
-
(2000)
Pediatr Nephrol
, vol.14
, pp. 143-145
-
-
Mourani, C.C.1
Sanjad, S.A.2
Akatcherian, C.Y.3
-
20
-
-
0030968154
-
Longterm follow-up of a girl with the neonatal form of Bartter's syndrome
-
Nakagawa Y, Toya K, Natsume H, et al: Longterm follow-up of a girl with the neonatal form of Bartter's syndrome. Endocr J 1997; 44:275-281
-
(1997)
Endocr J
, vol.44
, pp. 275-281
-
-
Nakagawa, Y.1
Toya, K.2
Natsume, H.3
-
21
-
-
0021966716
-
Bartter syndrome in two siblings: Antenatal and neonatal observations
-
Proesmans W, Devlieger H, Van Assche A, et al: Bartter syndrome in two siblings: Antenatal and neonatal observations. Int J. Pediatr Nephrol 1985; 6:63-70
-
(1985)
Int J. Pediatr Nephrol
, vol.6
, pp. 63-70
-
-
Proesmans, W.1
Devlieger, H.2
Van Assche, A.3
-
22
-
-
0031013269
-
Bartter's syndrome in pregnancy: A case report and review
-
O'Sullivan E, Monga M, Graves W: Bartter's syndrome in pregnancy: A case report and review. Am J Perinatol 1997; 14:55-57
-
(1997)
Am J Perinatol
, vol.14
, pp. 55-57
-
-
O'Sullivan, E.1
Monga, M.2
Graves, W.3
-
23
-
-
0034832453
-
Evaluation of long-term treatment with indomethacin in hereditary hypokalemic salt-losing tubulopathies
-
Reinalter SC, Grone HJ, Konrad M, et al: Evaluation of long-term treatment with indomethacin in hereditary hypokalemic salt-losing tubulopathies. J Pediatr 2001; 139:398-406
-
(2001)
J Pediatr
, vol.139
, pp. 398-406
-
-
Reinalter, S.C.1
Grone, H.J.2
Konrad, M.3
-
24
-
-
0019961848
-
Neonatal Bartter's syndrome, indomethacin and necrotizing enterocolitis
-
Marlow N, Chiswick ML. Neonatal Bartter's syndrome, indomethacin and necrotizing enterocolitis. Acta Paediatr Scand 1982; 71: 1031-1032
-
(1982)
Acta Paediatr Scand
, vol.71
, pp. 1031-1032
-
-
Marlow, N.1
Chiswick, M.L.2
-
25
-
-
0034942803
-
Selektive Cyclooxygenase- 2-Hemmer Pharmakologie und Kenntnisstand nach Markteinfuhrung
-
Schmidt H, Geisslinger G: Selektive Cyclooxygenase- 2-Hemmer Pharmakologie und Kenntnisstand nach Markteinfuhrung. Schmerz 2001; 15:207-219
-
(2001)
Schmerz
, vol.15
, pp. 207-219
-
-
Schmidt, H.1
Geisslinger, G.2
-
27
-
-
0035408815
-
Hypokalemic salt-losing tubulopathy with chronic renal failure and sensorineural deafness
-
Jeck N, Reinalter SC, Henne T, et al: Hypokalemic salt-losing tubulopathy with chronic renal failure and sensorineural deafness. Pediatrics 2001; 108:E5
-
(2001)
Pediatrics
, vol.108
-
-
Jeck, N.1
Reinalter, S.C.2
Henne, T.3
-
28
-
-
0035189356
-
Mutation of BSND causes Bartter syndrome with sensorineural deafness and kidney failure
-
Birkenhager R, Otto E, Schurmann MJ, et al: Mutation of BSND causes Bartter syndrome with sensorineural deafness and kidney failure. Nat Genet 2001; 29:310-4
-
(2001)
Nat Genet
, vol.29
, pp. 310-314
-
-
Birkenhager, R.1
Otto, E.2
Schurmann, M.J.3
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