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符合X连锁显性遗传的Alport综合征一家系21例调查报告 被引量:1

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出处 《中国实验诊断学》 2002年第2期119-119,共1页 Chinese Journal of Laboratory Diagnosis
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参考文献3

  • 1[1]Excerpts form United States Renal Data Systen 1997 Annual Re port: Incidence and prevalence of ESRD[J]. Am J Kidney Dis, 1997,30:40.
  • 2[2]Kashtan CE:Alport syndrome: An inherited disorder of renal, ocular and cochlear basementmembranes[J]. Medicine(Baltimore) , 1999,78(5):338.
  • 3[3]Buzza M, Wang YY, Dagher H, et al. COL4A4 mutation in thin basement membrane disease previously described in Alportsyndrome[J]. Kidney Int,2001,60(2) :480.

同被引文献5

  • 1Flinter FA, Cameron JS, Chantler C, et al. Genetics of classic Alport's Syndrome. Lancet, 1988, 2(5) : 1005-1007.
  • 2Chen D, Jefferson B, Harvey SJ, et al. Cyclosporine A slows the progressive renal disease of Alport Syndrome (X-Linked hereditary nephritis) : results from a eanine model. J Am Soe Nephrol, 2003, 14 (3): 690-698.
  • 3Cohen EP, Lemann JJ. In hereditary nephritis angiotesion-converting enzyme inhibition decreases proteinuria and may slow the rate of progression. Am J Kidney Dis, 1996, 27(2): 199-203.
  • 4Gobel J, Olbricht CJ, Offner G, et al. Kidney transplantation in Alport's Syndrome: long-term outcome and allograft anti-GBM nephritis. Clin Nephrol, 1992, 38(6):299-304.
  • 5汤伟光.Alport综合征的基因研究进展[J].医学综述,2002,8(8):446-448. 被引量:4

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