Familial Hyperkalemic Hypertension: A New Early-onset Pediatric Case.
作者信息
Pela Ivana
机构信息
Department of Sciences for Woman and Child's Health, University of Florence, Florence, Italy.
出版信息
Clin Pediatr Endocrinol. 2012 Jan;21(1):5-9. doi: 10.1297/cpe.21.5. Epub 2012 Feb 8.
Abstract
摘要
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本文引用的文献
1
Effect of age and affection status on blood pressure, serum potassium and stature in familial hyperkalaemia and hypertension.家族性高血钾-高血压中年龄和情感状态对血压、血钾和身高的影响。
Nephrol Dial Transplant. 2011 May;26(5):1547-53. doi: 10.1093/ndt/gfq612. Epub 2010 Oct 18.
2
The thiazide-sensitive Na-Cl cotransporter is regulated by a WNK kinase signaling complex.噻嗪类敏感的钠氯协同转运蛋白受WNK激酶信号复合体调控。
J Clin Invest. 2007 Nov;117(11):3403-11. doi: 10.1172/JCI32033.
3
WNK4 enhances TRPV5-mediated calcium transport: potential role in hypercalciuria of familial hyperkalemic hypertension caused by gene mutation of WNK4.WNK4增强TRPV5介导的钙转运：WNK4基因突变所致家族性高血钾性高血压高钙尿症中的潜在作用。
Am J Physiol Renal Physiol. 2007 Feb;292(2):F545-54. doi: 10.1152/ajprenal.00187.2006. Epub 2006 Oct 3.
4
Role of with-no-lysine [K] kinases in the pathogenesis of Gordon's syndrome.无赖氨酸[K]激酶在戈登综合征发病机制中的作用。
Pediatr Nephrol. 2006 Sep;21(9):1231-6. doi: 10.1007/s00467-006-0106-6. Epub 2006 May 9.
5
Familial hyperkalemic hypertension.
J Am Soc Nephrol. 2006 Jan;17(1):208-17. doi: 10.1681/ASN.2005030314. Epub 2005 Oct 12.
6
Hypercalciuria in familial hyperkalemia and hypertension accompanies hyperkalemia and precedes hypertension: description of a large family with the Q565E WNK4 mutation.家族性高钾血症和高血压中的高钙尿症伴随高钾血症并先于高血压出现：一个携带Q565E WNK4突变的大家族的描述。
J Clin Endocrinol Metab. 2004 Aug;89(8):4025-30. doi: 10.1210/jc.2004-0037.
7
HYPERTENSION AND HYPERPOTASSAEMIA WITHOUT RENAL DISEASE IN A YOUNG MALE.一名年轻男性无肾脏疾病情况下的高血压与高钾血症
Med J Aust. 1964 Aug 22;2:305-6. doi: 10.5694/j.1326-5377.1964.tb115766.x.
8
Human hypertension caused by mutations in WNK kinases.由WNK激酶突变引起的人类高血压。
Science. 2001 Aug 10;293(5532):1107-12. doi: 10.1126/science.1062844.
9
Molecular mechanisms of human hypertension.人类高血压的分子机制
Cell. 2001 Feb 23;104(4):545-56. doi: 10.1016/s0092-8674(01)00241-0.
10
Neonatal presentation of Gordon syndrome.
J Pediatr. 1996 Oct;129(4):615-7. doi: 10.1016/s0022-3476(96)70131-2.
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