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Fabry病及其酶替代疗法 被引量:9

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作者 张苏华 尹广
出处 《肾脏病与透析肾移植杂志》 CAS CSCD 2004年第6期560-565,共6页 Chinese Journal of Nephrology,Dialysis & Transplantation
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参考文献31

  • 1Brady RO, Gal AE, Bradley RM, et al. Enzymatic defect in Fabry's disease. Ceramidetrihexosidase deficiency. N. Engl. J. Med, 1967,276(21) :1163
  • 2Whybra C,Kampamann C,Willers I,et al. Anderson-Fabry disease:clinical manifestations of disease in female heterozygotes. J Inherit metab Dis,2001,24:715
  • 3Farge D, Nadlers, Wolfe LS,et al. Diagnostic value of kidney biopsy in heterozygous Fabry's disease. Arch Pathol Lab Med, 1985,109:85
  • 4Pastores GM, Lien YH. Biochemical and molecular genetic basis of Fabry disease [J]. J Am Soc Nephrol ,2002, 13 (Suppl 2 ): S130
  • 5Peters FP, Vermeulen A ,Kho TL. Anderson-Fabry's disease : alpha-galactosidase deficiency [J]. Lancet,2001 ,357:138
  • 6Sakuraba H,Oshima A,Fukuhara Y,et al. Identification of point mutations in the alpha-galactosidase A gene in classical and atypical hemizygotes with Fabry diseaseJ]. Am J Hum Genet, 1990,47:784
  • 7Von Scheidt W,Eng CM,Fitzmaurice TF,et al. An atypical variant of Fabry's disease with manifestations confined to the myocardium J]. N Engl J Med, 1991,324:395
  • 8陈惠萍,曾彩虹,朱茂艳.Fabry病[J].肾脏病与透析肾移植杂志,1997,6(3):285-288. 被引量:12
  • 9Alroy J,Sabnis S,Kopp JB. Renal pathology in Fabry disease[J]. J Am Soc Nephrol, 2002,13 ( Suppl 2 ): S 134
  • 10Thadhani R ,Wolf M, West ML, et al. Patients with Fabry disease on dialysis in the United States. Kidney Int,2002,61: 249

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