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Results: 1 to 20 of 119

1.

Eplerenone improved hypokalemia in a patient with Gitelman's syndrome.

Ito Y, Yoshida M, Nakayama M, Tsutaya S, Ogawa K, Maeda H, Miyata M, Oiso Y.

Intern Med. 2012;51(1):83-6. Epub 2012 Jan 1.

PMID:
22214629
[PubMed - indexed for MEDLINE]
Free Article
2.

Eplerenone for gitelman syndrome in pregnancy.

Morton A, Panitz B, Bush A.

Nephrology (Carlton). 2011 Mar;16(3):349. doi: 10.1111/j.1440-1797.2010.01396.x. No abstract available.

PMID:
21342329
[PubMed - indexed for MEDLINE]
3.

Hypokalemic rhabdomyolysis in a child with Gitelman's syndrome.

Kumagai H, Matsumoto S, Nozu K.

Pediatr Nephrol. 2010 May;25(5):953-5. doi: 10.1007/s00467-009-1412-6.

PMID:
20072789
[PubMed - indexed for MEDLINE]
4.

Gitelman syndrome as a cause of psychomotor retardation in a toddler.

Skalova S, Neuman D, Lnenicka P, Stekrova J.

Arab J Nephrol Transplant. 2013 Jan;6(1):37-9.

PMID:
23282232
[PubMed - indexed for MEDLINE]
Free Article
5.

A novel compound heterozygous mutation of Gitelman's syndrome in Japan, as diagnosed by an extraordinary response of the fractional excretion rate of chloride in the trichlormethiazide loading test.

Ueda K, Makita N, Kawarazaki H, Fujiwara T, Unuma S, Monkawa T, Hayashi M, Fujita T.

Intern Med. 2012;51(12):1549-53. Epub 2012 Jun 15.

PMID:
22728489
[PubMed - indexed for MEDLINE]
Free Article
6.

Gitelman's syndrome with vomiting manifested by severe metabolic alkalosis and progressive renal insufficiency.

Lee JH, Lee J, Han JS.

Tohoku J Exp Med. 2013;231(3):165-9.

PMID:
24162365
[PubMed - indexed for MEDLINE]
Free Article
7.

A novel initial codon mutation of the thiazide-sensitive Na-Cl cotransporter gene in a Japanese patient with Gitelman's syndrome.

Aoki K, Tajima T, Yabushita Y, Nakamura A, Nezu U, Takahashi M, Kimura M, Terauchi Y.

Endocr J. 2008 Jul;55(3):557-60. Epub 2008 Jun 3.

PMID:
18520105
[PubMed - indexed for MEDLINE]
Free Article
8.

Spironolactone versus eplerenone for the treatment of idiopathic hyperaldosteronism.

Karagiannis A, Tziomalos K, Papageorgiou A, Kakafika AI, Pagourelias ED, Anagnostis P, Athyros VG, Mikhailidis DP.

Expert Opin Pharmacother. 2008 Mar;9(4):509-15. doi: 10.1517/14656566.9.4.509.

PMID:
18312153
[PubMed - indexed for MEDLINE]
9.

Gitelman's syndrome: report of one case.

Chan CF, Mu SC, Lau BH, Chang CJ, Lin SH.

Acta Paediatr Taiwan. 2008 Jan-Feb;49(1):31-4.

PMID:
18581727
[PubMed - indexed for MEDLINE]
10.

Loss of consciousness and hypokalemia in an elderly man with a mutation of the thiazide-sensitive Na-Cl cotransporter gene.

Hashida T, Yamada M, Hashimoto K, Satoh T, Okada S, Shibusawa N, Ishizuka T, Mori M.

Endocr J. 2006 Dec;53(6):859-63. Epub 2006 Sep 12.

PMID:
16966826
[PubMed - indexed for MEDLINE]
Free Article
11.

[Gitelman's syndrome: an important differential diagnosis of hypokalemia].

Kurschat C, Heering P, Grabensee B.

Dtsch Med Wochenschr. 2003 May 30;128(22):1225-8. German.

PMID:
12772080
[PubMed - indexed for MEDLINE]
12.

Gitelman's syndrome: a pathophysiological and clinical update.

Nakhoul F, Nakhoul N, Dorman E, Berger L, Skorecki K, Magen D.

Endocrine. 2012 Feb;41(1):53-7. doi: 10.1007/s12020-011-9556-0. Epub 2011 Nov 15. Review.

PMID:
22169961
[PubMed - indexed for MEDLINE]
13.

Gitelman syndrome: novel mutation and long-term follow-up.

Sinha A, Lněnička P, Basu B, Gulati A, Hari P, Bagga A.

Clin Exp Nephrol. 2012 Apr;16(2):306-9. doi: 10.1007/s10157-011-0542-x. Epub 2011 Oct 4.

PMID:
21964762
[PubMed - indexed for MEDLINE]
14.

Phenotype-genotype correlation and follow-up in adult patients with hypokalaemia of renal origin suggesting Gitelman syndrome.

Balavoine AS, Bataille P, Vanhille P, Azar R, Noël C, Asseman P, Soudan B, Wémeau JL, Vantyghem MC.

Eur J Endocrinol. 2011 Oct;165(4):665-73. doi: 10.1530/EJE-11-0224. Epub 2011 Jul 13.

PMID:
21753071
[PubMed - indexed for MEDLINE]
Free Article
15.

Genotype, phenotype, and follow-up in Taiwanese patients with salt-losing tubulopathy associated with SLC12A3 mutation.

Tseng MH, Yang SS, Hsu YJ, Fang YW, Wu CJ, Tsai JD, Hwang DY, Lin SH.

J Clin Endocrinol Metab. 2012 Aug;97(8):E1478-82. doi: 10.1210/jc.2012-1707. Epub 2012 Jun 7.

PMID:
22679066
[PubMed - indexed for MEDLINE]
16.

Two novel genotypes of the thiazide-sensitive Na-Cl cotransporter (SLC12A3) gene in patients with Gitelman's syndrome.

Aoi N, Nakayama T, Tahira Y, Haketa A, Yabuki M, Sekiyama T, Nakane C, Mano H, Kawachi H, Sato N, Soma M, Matsumoto K.

Endocrine. 2007 Apr;31(2):149-53.

PMID:
17873326
[PubMed - indexed for MEDLINE]
17.

A case of Gitelman syndrome associated with idiopathic intracranial hypertension.

Tsutsui H, Hamano T, Kawaura Y, Inaba S, Miyamori I, Yasujima M, Yoneda M, Kuriyama M.

Intern Med. 2011;50(14):1493-6. Epub 2011 Jul 15.

PMID:
21757836
[PubMed - indexed for MEDLINE]
Free Article
18.

[Gitelman syndrome: a crucial role of laboratory medicine for the diagnosis].

Murienne B, Pointet P, Beaune G.

Ann Biol Clin (Paris). 2013 Mar-Apr;71(2):235-9. doi: 10.1684/abc.2013.0791. French.

PMID:
23587595
[PubMed - indexed for MEDLINE]
19.

Novel mutations in the SLC12A3 gene causing Gitelman's syndrome in Swedes.

Fava C, Montagnana M, Rosberg L, Burri P, Jönsson A, Wanby P, Wahrenberg H, Hulthén UL, Aurell M, Guidi GC, Melander O.

DNA Seq. 2007 Oct;18(5):395-9.

PMID:
17654016
[PubMed - indexed for MEDLINE]
20.

It is never too late for a genetic disease: a case of a 79-year-old man with persistent hypokalemia.

Brambilla G, Perotti M, Perra S, Dell'Oro R, Grassi G, Pincelli AI.

J Nephrol. 2013 May-Jun;26(3):594-8. doi: 10.5301/jn.5000256. Epub 2013 Mar 6.

PMID:
23475471
[PubMed - indexed for MEDLINE]

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