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Nephrology Dialysis Transplantation

Volumn 15, Issue SUPPL. 6, 2000, Pages 19-20

The diuretic- and Bartter-like salt-losing tubulopathies

(4) Jeck, N a Konrad, M a Hess, M a Seyberth, H W a

a PHILIPPS UNIVERSITY MARBURG (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

ALDOSTERONE; CALCIUM; CARRIER PROTEIN; CHLORIDE; DIURETIC AGENT; FUROSEMIDE; INDOMETACIN; LOOP DIURETIC AGENT; MAGNESIUM; POTASSIUM; POTASSIUM CHANNEL; PROSTAGLANDIN E; RENIN; SODIUM; SODIUM CHLORIDE; THIAZIDE DIURETIC AGENT; WATER;

ARTICLE; BARTTER SYNDROME; CALCIUM TRANSPORT; CALCIUM URINE LEVEL; CHLORIDE TRANSPORT; CLINICAL ARTICLE; CLINICAL FEATURE; CONTROLLED STUDY; DEHYDRATION; DISEASE SEVERITY; DIURESIS; DRUG TARGETING; GENE MUTATION; GITELMAN SYNDROME; HETEROZYGOSITY; HUMAN; HYDRAMNIOS; HYPOKALEMIA; HYPOMAGNESEMIA; INFANT; KIDNEY CALCIFICATION; KIDNEY TUBULE ABSORPTION; PATHOPHYSIOLOGY; PHENOTYPE; POTASSIUM TRANSPORT; PRIORITY JOURNAL; RENIN ANGIOTENSIN ALDOSTERONE SYSTEM; SALT LOSING NEPHRITIS; SODIUM TRANSPORT;

EID: 0033661429 PISSN: 09310509 EISSN: None Source Type: Journal
DOI: 10.1093/ndt/15.suppl_6.19 Document Type: Article

Times cited : (11)

References (14)

1
- 0002660675
- Hypokalemic tubular disorders: The hyperprostaglandin E syndrome and the Bartter-Gitelman syndrome
- Davison AM, Cameron JS, Grunfeld J-P et al. eds. Oxford Textbook of Clinical Nephrology. Oxford Medical Publications, Oxford.
- (1998) , pp. 1085-1094
- Seyberth, H.W.¹ Soergel, M.² Kockerling, A.³

2
- 0013976561
- A new familial disorder characterized by hypokalemia and hypomagnesemia
- (1966) Trans Assoc Am Physicians , vol.79 , pp. 221-223
- Gitelman, H.J.¹ Graham, J.B.² Welt, L.G.³

3
- 50849151835
- Hyperplasia of the juxtaglomerular complex with hyperaldosteronism and hypokalemic alkalosis-a new syndrome
- (1962) Am J Med , vol.33 , pp. 811-828
- Bartter, F.C.¹ Pronove, P.² Gill, J.R.³

4
- 0022251369
- Congenital hypokalemia with hypercalciuria in preterm infants: A hyperprostaglandinuric tubular syndrome different from Bartter syndrome
- (1985) J Pediatr , vol.107 , pp. 694-701
- Seyberth, H.W.¹ Rascher, W.² Schweer, H.³

5
- 9044235777
- Gitelman's variant of Bartter's syndrome, inherited hypokalemic alkalosis, is caused by mutations in the thiazide-sensitive Na-Cl cotransporter
- (1996) Nature Genet , vol.12 , pp. 24-30
- Simon, D.B.¹ Nelson-Williams, C.² Bia, M.J.³

6
- 16944366243
- Mutations in the chloride channel gene, CLCNKB, cause Bartter's syndrome type III
- (1997) Nature Genet , vol.17 , pp. 171-178
- Simon, D.B.¹ Bindra, R.S.² Mansfield, T.A.³

7
- 0033914432
- Mutations in the chloride channel gene, CLCNKB, cause Bartter syndrome
- (2000) J Am Soc Nephrol , vol.11 , pp. 1449-1459
- Konrad, M.¹ Vollmer, M.² Lemmink, H.³

8
- 0030851745
- Localization and induction by dehydration of ClC-K chloride channels in the rat kidney
- (1997) Am J Physiol , vol.272
- Vandewalle, A.¹ Cluzeaud, F.² Bens, M.³

9
- 0030032699
- Bartter's syndrome, hypokalemic alkalosis with hypercalciuria, is caused by mutations in the Na-K-2Cl cotransporter NKCC2
- (1996) Nature Genet , vol.13 , pp. 183-188
- Simon, D.B.¹ Karet, F.E.² Hamdan, J.M.³

10
- 0029794875
- + channel, ROMK
- (1996) Nature Genet , vol.14 , pp. 152-156
- Simon, D.B.¹ Karet, F.E.² Rodriguez-Soriano, J.³

11
- 8044222737
- Mutations in the gene encoding the inwardly-rectifying renal potassium channel, ROMK, cause the antenatal variant of Bartter syndrome: Evidence for genetic heterogeneity
- (1997) Hum Mol Genet , vol.6 , pp. 17-26
- Karolyi, L.¹ Konrad, M.² Kockerling, A.³

12
- 0021871604
- Ion transport mechanisms in thick ascending limb of Henle's loop of mammalian nephron
- (1985) Physiol Rev , vol.65 , pp. 760-797
- Greger, R.¹

13
- 0031831767
- Renal potassium transport: Mechanism and regulation
- (1998) Am J Physiol , vol.274
- Giebisch, G.¹

14
- 0032432570
- K-Cl cotransporter expression in the human kidney
- (1998) Am J Physiol , vol.275
- Liapis, H.¹ Nag, M.² Kaji, D.M.³

* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.