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Items: 1 to 20 of 110

1.

Genetic disorders of potassium homeostasis.

Jain G, Ong S, Warnock DG.

Semin Nephrol. 2013 May;33(3):300-9. doi: 10.1016/j.semnephrol.2013.04.010. Review.

PMID:
23953807
2.

Inherited forms of mineralocorticoid hypertension.

Hassan-Smith Z, Stewart PM.

Curr Opin Endocrinol Diabetes Obes. 2011 Jun;18(3):177-85. doi: 10.1097/MED.0b013e3283469444. Review.

PMID:
21494136
3.

Understanding Bartter syndrome and Gitelman syndrome.

Fremont OT, Chan JC.

World J Pediatr. 2012 Feb;8(1):25-30. doi: 10.1007/s12519-012-0333-9. Epub 2012 Jan 27. Review.

PMID:
22282380
4.

Inherited forms of mineralocorticoid hypertension.

Zennaro MC, Boulkroun S, Fernandes-Rosa F.

Best Pract Res Clin Endocrinol Metab. 2015 Aug;29(4):633-45. doi: 10.1016/j.beem.2015.04.010. Epub 2015 May 5. Review.

PMID:
26303089
5.

Apparent mineralocorticoid excess syndrome: report of one family with three affected children.

Al-Harbi T, Al-Shaikh A.

J Pediatr Endocrinol Metab. 2012;25(11-12):1083-8. doi: 10.1515/jpem-2012-0113.

PMID:
23329753
6.

Abnormalities of aldosterone synthesis and action in children.

White PC.

Curr Opin Pediatr. 1997 Aug;9(4):424-30. Review.

PMID:
9300202
7.

[Bartter syndrome, Gitelman syndrome, Liddle syndrome].

Takeuchi K.

Nihon Rinsho. 2002 Jan;60 Suppl 1:532-40. Review. Japanese. No abstract available.

PMID:
11838164
8.

Hyper- and hypoaldosteronism.

Torpy DJ, Stratakis CA, Chrousos GP.

Vitam Horm. 1999;57:177-216. Review.

PMID:
10232050
9.

Low-renin hypertension of childhood.

Parsa AA, New MI.

Endocrinol Metab Clin North Am. 2011 Jun;40(2):369-77, viii. doi: 10.1016/j.ecl.2011.01.004.

PMID:
21565672
10.

Liddle syndrome: genetics and mechanisms of Na+ channel defects.

Warnock DG.

Am J Med Sci. 2001 Dec;322(6):302-7. Review.

PMID:
11780687
11.

[Bartter and Gitelman syndromes].

Brochard K.

Arch Pediatr. 2015 May;22(5 Suppl 1):46-7. doi: 10.1016/S0929-693X(15)30024-5. French. No abstract available.

PMID:
26112515
12.

Potassium-related inherited tubulopathies.

Landau D.

Cell Mol Life Sci. 2006 Sep;63(17):1962-8. Review.

PMID:
16810456
13.

Bartter syndrome presenting as poor weight gain and abdominal mass in an infant.

Heffernan A, Steffensen TS, Gilbert-Barness E, Perlman S.

Fetal Pediatr Pathol. 2008;27(4-5):232-43. doi: 10.1080/15513810802216010.

PMID:
18800266
14.

Advances in genetic hypertension.

Williams SS.

Curr Opin Pediatr. 2007 Apr;19(2):192-8. Review.

PMID:
17496764
15.

Case report: severe neonatal hyperkalemia due to pseudohypoaldosteronism type 1.

Schweiger B, Moriarty MW, Cadnapaphornchai MA.

Curr Opin Pediatr. 2009 Apr;21(2):269-71. doi: 10.1097/MOP.0b013e328325a55f.

PMID:
19657313
16.

Monogenic forms of hypertension.

Simonetti GD, Mohaupt MG, Bianchetti MG.

Eur J Pediatr. 2012 Oct;171(10):1433-9. Epub 2011 Mar 15. Review.

PMID:
21404100
17.

[An asymptomatic chronic hypokalaemia].

Otto MP, Cheminel V, Crevon L, Dubourg L, Hadj-Aissa A, Mounier C, Prevosto JM.

Ann Biol Clin (Paris). 2011 Jul-Aug;69(4):459-64. doi: 10.1684/abc.2011.0597. French.

18.

Bartter and Gitelman syndromes.

Schurman SJ, Shoemaker LR.

Adv Pediatr. 2000;47:223-48. Review.

PMID:
10959445
19.

[Monogenic hypertension].

Maier T, Hoyer J.

Dtsch Med Wochenschr. 2006 Nov 17;131(46):2601-4. Review. German. No abstract available.

PMID:
17096307
20.

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.

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