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干燥综合征肾脏受累合并代谢性碱中毒1例 被引量:3

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摘要 患者,女,56岁,因眼干5年、双下肢无力2年余于2011年8月18日入院。2006年8月双眼于涩,无口干。2007年3月外院诊为“双干眼症”。
出处 《临床荟萃》 CAS 2013年第2期221-222,共2页 Clinical Focus
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参考文献6

  • 1王海燕.肾脏病学[M]北京:人民卫生出版社,2009319-320.
  • 2Chen YC,Yang WC,Yang AH. Primary Sj(o)gren' s syndrome associated with Gitelman's syndrome presenting with muscular paralysis[J].American Journal of Kidney Diseases,2003,(03):586-590.
  • 3Schwarz C,Barisani T,Bauer E. A woman with red eye and hypokalemia:a case of acquired Gitelman' s syndrome[J].Wiener Klinische Wochenschrift,2006,(7/8):239-242.
  • 4Kim YK,Song HC,Kim WY. Acquired Gitelman syndrome in a patient with primary Sj(o)gren syndrome[J].American Journal of Kidney Diseases,2008,(06):1163-1167.doi:10.1053/j.ajkd.2008.07.025.
  • 5孙明姝,潘琳,梁宏达,王吉波.疑诊为干燥综合征的Gitelman综合征一例[J].中华风湿病学杂志,2009,13(10):726-727. 被引量:2
  • 6秦岭,陈楠.Gitelman综合征[J].肾脏病与透析肾移植杂志,2008,17(1):72-75. 被引量:10

二级参考文献30

  • 1于迎,冯晓蓓,孟晓慧,李桂梅,任红,张文,潘晓霞,陈楠.遗传性低钾失盐性肾小管病临床分析[J].肾脏病与透析肾移植杂志,2007,16(2):141-145. 被引量:11
  • 2邵乐平,任红,王伟铭,张文,李晓,潘晓霞,宋怀东,陈楠.Gitelman综合征SLC12A3基因突变研究[J].中华肾脏病杂志,2007,23(6):351-356. 被引量:24
  • 3Melander O, Orho-Melander M, Bengtsson K, et al. Genetic variants of thiazide- sensitive NaCl cotransporter in Gitelman's syndrome and primary hypertension. Hypertension, 2000, 36:389 - 394.
  • 4Kial YK, Song HC, Kim WY, et al. Acquired Gitelman's syndrome in a patient with primary Sjogren's syndrome. AJKD, 2008, 52:1163-1167.
  • 5Bettinelli A, Bianehetti MG, Girardin E, et al. Use of calcium excretion values to distinguish two forms of primary renal tubular hypokalemic alkalosis: Bartter and Gitehnan syndromes. J Pediatr, 1992, 120: 38-43.
  • 6Rodriguez-Soriano J. Bartter and related syndromes: the puzzle is almost solved. Pediatr Nephrol, 1998, 12: 315-327.
  • 7Gitelman HJ, Graham JB, Welt LG. A new familial disorder characterized by hypokalemia and hypomagnesemia. Trans Assoc Am Physicians, 1966,79:221 - 235.
  • 8Seyberth H, Soergel M, Koeckerling A. Hypokalaemic tubular disorders: The hyperprostaglandin E syndrome and Gitelman-Bartter syndrome. In: Oxford Textbook of Clinical Nephrology,2nd ed, Davison AM, Cameron JS, Gru nfeld JP, Kerr DN, Ritz E,eds. Oxford, Oxford University Press, 1998, 1085 - 1094.
  • 9Tago N, Kokubo Y, Inamoto N, et al. A high prevalence of Gitelman's syndrome mutations in Japanese. Hypertens Res,2004,27 (5) :327 -331.
  • 10Riveira-munoz E, Chang Q, Godefroid N, et al. Transcriptional and Functional Analyses of SLC12A3Mutations: New Clues for the Pathogenesis of Gitelman Syndrome. J Am Soc Nephrol, 2007, 18 : 1271 - 1283.

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