Display Settings:

Format
Items per page
Sort by

Send to:

Choose Destination

Results: 1 to 20 of 130

1.

Bartter syndrome type III and congenital anomalies of the kidney and urinary tract: an antenatal presentation.

Westland R, Hack WW, van der Horst HJ, Uittenbogaard LB, van Hagen JM, van der Valk P, Kamsteeg EJ, van den Heuvel LP, van Wijk JA.

Clin Nephrol. 2012 Dec;78(6):492-6.

PMID:
23164417
[PubMed - indexed for MEDLINE]
2.

Mutations in the chloride channel gene CLCNKB as a cause of classic Bartter syndrome.

Konrad M, Vollmer M, Lemmink HH, van den Heuvel LP, Jeck N, Vargas-Poussou R, Lakings A, Ruf R, Deschênes G, Antignac C, Guay-Woodford L, Knoers NV, Seyberth HW, Feldmann D, Hildebrandt F.

J Am Soc Nephrol. 2000 Aug;11(8):1449-59.

PMID:
10906158
[PubMed - indexed for MEDLINE]
Free Article
3.

Simultaneous mutations in the CLCNKB and SLC12A3 genes in two siblings with phenotypic heterogeneity in classic Bartter syndrome.

Bettinelli A, Borsa N, Syrén ML, Mattiello C, Coviello D, Edefonti A, Giani M, Travi M, Tedeschi S.

Pediatr Res. 2005 Dec;58(6):1269-73.

PMID:
16306206
[PubMed - indexed for MEDLINE]
4.

Inherited primary renal tubular hypokalemic alkalosis: a review of Gitelman and Bartter syndromes.

Shaer AJ.

Am J Med Sci. 2001 Dec;322(6):316-32. Review.

PMID:
11780689
[PubMed - indexed for MEDLINE]
5.

A founder mutation in the CLCNKB gene causes Bartter syndrome type III in Spain.

Rodríguez-Soriano J, Vallo A, Pérez de Nanclares G, Bilbao JR, Castaño L.

Pediatr Nephrol. 2005 Jul;20(7):891-6. Epub 2005 May 5.

PMID:
15875219
[PubMed - indexed for MEDLINE]
6.

[Bartter's syndromes].

Vantyghem MC, Douillard C, Binaut R, Provot F.

Ann Endocrinol (Paris). 1999 Dec;60(6):465-72. Review. French.

PMID:
10617800
[PubMed - indexed for MEDLINE]
7.

Recurrent urinary tract infections in an infant with antenatal Bartter syndrome.

Tasic V, Pota L, Gucev Z.

World J Pediatr. 2011 Feb;7(1):86-8. doi: 10.1007/s12519-010-0021-6. Epub 2010 Feb 1.

PMID:
20127218
[PubMed - indexed for MEDLINE]
8.

A novel mutation in the chloride channel gene, CLCNKB, as a cause of Gitelman and Bartter syndromes.

Zelikovic I, Szargel R, Hawash A, Labay V, Hatib I, Cohen N, Nakhoul F.

Kidney Int. 2003 Jan;63(1):24-32.

PMID:
12472765
[PubMed - indexed for MEDLINE]
9.
10.

Gitelman or Bartter type 3 syndrome? A case of distal convoluted tubulopathy caused by CLCNKB gene mutation.

Cruz AJ, Castro A.

BMJ Case Rep. 2013 Jan 22;2013. pii: bcr2012007929. doi: 10.1136/bcr-2012-007929.

PMID:
23345488
[PubMed - indexed for MEDLINE]
11.
12.

Genotype-phenotype correlations in normotensive patients with primary renal tubular hypokalemic metabolic alkalosis.

Bettinelli A, Vezzoli G, Colussi G, Bianchetti MG, Sereni F, Casari G.

J Nephrol. 1998 Mar-Apr;11(2):61-9. Review.

PMID:
9589375
[PubMed - indexed for MEDLINE]
13.

A Spanish founder mutation in the chloride channel gene, CLCNKB, as a cause of atypical Bartter syndrome in adult age.

Gorgojo JJ, Donnay S, Jeck N, Konrad M.

Horm Res. 2006;65(2):62-8. Epub 2006 Jan 2.

PMID:
16391491
[PubMed - indexed for MEDLINE]
14.

Placental pathology in fetal bartter syndrome.

Ernst LM, Parkash V.

Pediatr Dev Pathol. 2002 Jan-Feb;5(1):76-9.

PMID:
11815871
[PubMed - indexed for MEDLINE]
15.

Molecular analysis of the CLCNKB gene in Japanese patients with classic Bartter syndrome.

Tajima T, Nawate M, Takahashi Y, Mizoguchi Y, Sugihara S, Yoshimoto M, Murakami M, Adachi M, Tachibana K, Mochizuki H, Fujieda K.

Endocr J. 2006 Oct;53(5):647-52. Epub 2006 Aug 11.

PMID:
16902263
[PubMed - indexed for MEDLINE]
Free Article
16.

A case of antenatal Bartter syndrome with sensorineural deafness.

Lee HS, Cheong HI, Ki CS.

J Pediatr Endocrinol Metab. 2010 Oct;23(10):1077-81.

PMID:
21158220
[PubMed - indexed for MEDLINE]
17.

Mutations in the chloride channel gene, CLCNKB, leading to a mixed Bartter-Gitelman phenotype.

Jeck N, Konrad M, Peters M, Weber S, Bonzel KE, Seyberth HW.

Pediatr Res. 2000 Dec;48(6):754-8.

PMID:
11102542
[PubMed - indexed for MEDLINE]
18.

Renal cysts and nephrocalcinosis in a patient with Bartter syndrome type III.

Watanabe T, Tajima T.

Pediatr Nephrol. 2005 May;20(5):676-8. Epub 2005 Feb 17.

PMID:
15717167
[PubMed - indexed for MEDLINE]
19.

Hypokalemic paralysis in a middle-aged female with classic Bartter syndrome.

Chiang WF, Lin SH, Chan JS, Lin SH.

Clin Nephrol. 2014 Feb;81(2):146-50. doi: 10.5414/CN107606.

PMID:
22854165
[PubMed - indexed for MEDLINE]
20.

Phenotype-genotype correlation in antenatal and neonatal variants of Bartter syndrome.

Brochard K, Boyer O, Blanchard A, Loirat C, Niaudet P, Macher MA, Deschenes G, Bensman A, Decramer S, Cochat P, Morin D, Broux F, Caillez M, Guyot C, Novo R, Jeunemaître X, Vargas-Poussou R.

Nephrol Dial Transplant. 2009 May;24(5):1455-64. doi: 10.1093/ndt/gfn689. Epub 2008 Dec 18.

PMID:
19096086
[PubMed - indexed for MEDLINE]
Free Article

Display Settings:

Format
Items per page
Sort by

Send to:

Choose Destination

Supplemental Content

Write to the Help Desk