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Gitelman综合征1例报告 被引量:3

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出处 《内科急危重症杂志》 2007年第1期53-54,共2页 Journal of Critical Care In Internal Medicine
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参考文献3

  • 1Guay-Woodford LM.Bartter Syndrome:Unraveling the pathophysiologic enigma.Am J Med,1998,105:151. 被引量:1
  • 2Simon DB,Lifton RP.Mutations in Na (K)Cl transporters in Gitelman's and Bartter's syndromes.Curt Opin Cell Biol,1998,10:450. 被引量:1
  • 3胡蜀红,敖华.Bartter综合征1例[J].内科急危重症杂志,2002,8(4):224-224. 被引量:4

二级参考文献4

  • 1Bartter FC, Pronove P, Gill JR, et al. Hyperplasia of the juxtaglomerular apparatus with hyperaldosteronism and hypokalemic alkalosis: a new syndrome. Am. J. Med. 1962,33:811. 被引量:1
  • 2王平芳,廖二元.肾脏与内分泌.见:廖二元,赵楚生主编.内分泌学.北京:人民卫生出版社,2001.2208-2209. 被引量:3
  • 3Kokko JP, Renal dis esse. In: Cecil Textbook of Medicine. ed20.Ed. by Bennet J.C ,Plum.F. WB Saunders Company,1996. 598. 被引量:1
  • 4林善锬.遗传性肾小管疾病[J].中华内科杂志,2002,41(8):562-563. 被引量:1

共引文献3

同被引文献20

  • 1Seyberth HW, Schlingmann KP. Bartter- and Gitelman-like syn- dromes: salt-losing tubulopathies with loop or DCT defects[J]. Pedi- air Nephrol,2011,26(10) :1789-802. 被引量:1
  • 2Lee BH, Cho HY, Lee H, et al. Genetic basis of Bartter syndrome in Korea [ J ]. Ncphrol Dial Transplant,2012,27 (4) : 1516 -1521. 被引量:1
  • 3Zelikovic I,Szargel R,Hawash A,et al. A novel mutation in the chlo- ride channel gene, CLCNKB, as a cause of Gitelman and Bartter syn- dromes[ J]. Kidney Int,2003,63 ( 1 ) :24-32. 被引量:1
  • 4Urbanovd M1 ,Reitemvd J,St~krov6 J,et al. DNA analysis of renal e- lectrolyte transporter genes among patients suffering from Bartter and Gitelman syndromes : summary of mutation screening [ J ]. Folia Biol (Praha) ,2011,57(2) :6533. 被引量:1
  • 5Konrad M, Vollmer M, Lemmink HH, et al. Mutations in the chloride channel gene CLCNKB as a cause of classic Bartter syndrome[ J]. J Am Soc Nephrol,2000,11 (8) : 1449-1459. 被引量:1
  • 6Nozu K, Iijima K, Kanda K, et al. The pharmacological characteristics of molecular-based inherited salt-losing tubulopathies[ J]. J Clin En- docrinol Metab ,2010,95 ( 12 ) : E51 l-E518. 被引量:1
  • 7Garcia Castafio A1 , P6rez de Nanclares G, Madariaga L, et al. Genet- ics of type III Bartter syndrome in Spain, proposed diagnostic algo- rithm[J]. PLoS One,2013,18,8(9) :e74673. 被引量:1
  • 8Tajima T, Nawate M, Takahashi Y, et al. Molecular analysis of the CLCNKB gene in Japanese patients with classic Bartter syndrome [ J]. Endocr J,2006,53 (5) :647-652. 被引量:1
  • 9Fremont OT, Chan JC. Understanding Bartter syndrome and Gitelman syndrome[ J]. World J Pediatr,2012,8( 1 ) :25-30. 被引量:1
  • 10董晖,郎艳华,邵泽平,李林,邵乐平.Gitelman综合征合并甲状腺疾病:两例患者SLC12A3基因分析[J].中华内分泌代谢杂志,2010,26(5):395-398. 被引量:11

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