-
1
-
-
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., Ellison D., Karet F.E., Molina A.M., et al. Gitelman's variant of Bartter's syndrome, inherited hypokalaemic alkalosis, is caused by mutations in the thiazide-sensitive Na-Cl cotransporter. Nat. Genet. 12 (1996) 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
Molina, A.M.6
-
3
-
-
0037326120
-
A typical Bartter syndrome with sensorineural deafness with G47R mutation of the beta-subunit for ClC-Ka and ClC-Kb chloride channels, barttin
-
Miyamura N., Matsumoto K., Taguchi T., Tokunaga H., Nishikawa T., Nishida K., et al. A typical Bartter syndrome with sensorineural deafness with G47R mutation of the beta-subunit for ClC-Ka and ClC-Kb chloride channels, barttin. J. Clin. Endocrinol. Metab. 88 (2003) 781-786
-
(2003)
J. Clin. Endocrinol. Metab.
, vol.88
, pp. 781-786
-
-
Miyamura, N.1
Matsumoto, K.2
Taguchi, T.3
Tokunaga, H.4
Nishikawa, T.5
Nishida, K.6
-
4
-
-
0041382927
-
Hypokalaemic salt-losing tubulopathies: an evolving story
-
Zelikovic I. Hypokalaemic salt-losing tubulopathies: an evolving story. Nephrol. Dial. Transplant. 18 (2003) 1696-1700
-
(2003)
Nephrol. Dial. Transplant.
, vol.18
, pp. 1696-1700
-
-
Zelikovic, I.1
-
5
-
-
0037213896
-
A novel mutation in the chloride channel ge,e, CLC-NKB, as a cause of Gitelman and Bartter syndromes
-
Zelikovic I., Szargel R., Hawash A., Labay V., Hatib I., Cohen N., et al. A novel mutation in the chloride channel ge,e, CLC-NKB, as a cause of Gitelman and Bartter syndromes. Kidney Int. 63 (2003) 24-32
-
(2003)
Kidney Int.
, vol.63
, pp. 24-32
-
-
Zelikovic, I.1
Szargel, R.2
Hawash, A.3
Labay, V.4
Hatib, I.5
Cohen, N.6
-
6
-
-
33645456811
-
Nausea, emesis, and muscle weakness in a pregnant adolescent
-
Srinivas S.K., Sukhan S., and Elovitz M.A. Nausea, emesis, and muscle weakness in a pregnant adolescent. Obstet. Gynecol. 107 (2006) 481-482
-
(2006)
Obstet. Gynecol.
, vol.107
, pp. 481-482
-
-
Srinivas, S.K.1
Sukhan, S.2
Elovitz, M.A.3
-
7
-
-
2942571098
-
Is normalisation of serum potassium and magnesium always necessary in Gitelman syndrome for a successful obstetric outcome?
-
Basu A., Dillon R.D.S., Taylor R., Davison J.M., and Marshall S.M. Is normalisation of serum potassium and magnesium always necessary in Gitelman syndrome for a successful obstetric outcome?. Br. J. Obstet. Gynaecol. 111 (2004) 630-634
-
(2004)
Br. J. Obstet. Gynaecol.
, vol.111
, pp. 630-634
-
-
Basu, A.1
Dillon, R.D.S.2
Taylor, R.3
Davison, J.M.4
Marshall, S.M.5
-
8
-
-
0031697634
-
Outcome of two pregnancies in a patient with Gitelman's syndrome: a case report
-
Jones J.M., and Dorell S. Outcome of two pregnancies in a patient with Gitelman's syndrome: a case report. J Matern Fetal Invest 8 (1998) 147-148
-
(1998)
J Matern Fetal Invest
, vol.8
, pp. 147-148
-
-
Jones, J.M.1
Dorell, S.2
-
9
-
-
23944462389
-
Outcome of pregnancy in a patient with Gitelman syndrome: a case report
-
Talaulikar G.S., and Falk M.C. Outcome of pregnancy in a patient with Gitelman syndrome: a case report. Nephron Physiol. 101 (2005) 35-38
-
(2005)
Nephron Physiol.
, vol.101
, pp. 35-38
-
-
Talaulikar, G.S.1
Falk, M.C.2
-
10
-
-
0033044646
-
Gestational magnesium deficiency is deleterious to fetal outcome
-
Almonte R.A., Heath D.L., Whitehall J., Russell M., Patole S., and Vink R. Gestational magnesium deficiency is deleterious to fetal outcome. Biol. Neonate 76 (1999) 26-32
-
(1999)
Biol. Neonate
, vol.76
, pp. 26-32
-
-
Almonte, R.A.1
Heath, D.L.2
Whitehall, J.3
Russell, M.4
Patole, S.5
Vink, R.6
-
11
-
-
0033013437
-
Magnesium supplementation in Gitelman syndrome
-
Bettinelli A., Basilico E., Metta M.G., Borella P., Jaeger P., and Bianchetti M.G. Magnesium supplementation in Gitelman syndrome. Pediatr. Nephrol. 13 (1999) 311-314
-
(1999)
Pediatr. Nephrol.
, vol.13
, pp. 311-314
-
-
Bettinelli, A.1
Basilico, E.2
Metta, M.G.3
Borella, P.4
Jaeger, P.5
Bianchetti, M.G.6
|