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Fabry病的肾脏病变及诊治进展 被引量:4

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作者 李文歌
出处 《中国医师进修杂志(内科版)》 2006年第6期8-10,共3页 Chinese Journal of Postgraduates of Medicine
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参考文献14

  • 1Mssson C, Cisse I, Simon V, et al. Fabry disease: a review. Joint Bone Spine,2004, 71(5): 381-383.
  • 2Warnock DG. Fabry disease: diagnosis and management, with emphasis on the renal manifestation. Curr Opin Nephrol Hypertens,2005, 14: 87-95.
  • 3Alory J, Sabnis S, Kopp JB. Renal pathology in Fabry disease. J Am Soc Nephrol, 2002, 13(Suppl 2): s134-s138.
  • 4张苏华,刘志红,李世军,陈惠萍,苏健,曾彩虹,黎磊石.Fabry病的临床表现及肾脏病理学特征[J].肾脏病与透析肾移植杂志,2004,13(6):517-523. 被引量:16
  • 5Cybulla M, Schaefer E, Wendt S, et al. Chronic renal failure and proteinuria in adulthood: Fabry disease predominantly affecting the kidneys. Am J Kidney Dis, 2005,45: 82-89.
  • 6Branton M, Schiffman R, Kopp JB. Natural history and treatment of renal involvement in Fabry discase. J Am Soc Nephrol, 2002, 13(Suppl 2): s139-s143.
  • 7Sessa A, Meroni M, Battini G, et al. Chronic renal failure, dialysis, and renal transplantation in Anderson - Fabry disease. Semin Nephrol, 2004, 24: 532-536.
  • 8USAN Council. List No. 431. New names agalsidase alfa. Clin Pharmacol Ther,2000, 68(4): 456.
  • 9Clarke JT, Iwanochko RM. Enzyme replacement therapy of Fabry discase. Mol Neurobiol, 2005, 32: 43-50.
  • 10Robert JD, Brady R, Barranger J, et al. Fabry disease, an under-recognized multisystemic disorder: expert recommendations for diagnosis, management, and enzyme replacement therapy. Annals Intern Med, 2003, 138: 338-346.

二级参考文献17

  • 1Brady RO, Schiffmann R. Clinical features of and recent advances in therapy for Fabry disease [J]. JAMA, 2000,284: 2771
  • 2Brady RO, Gal AE, Bradley RM, et al. Enzymatic defect in Fabry 's disease. Ceramidetrihexosidase deficiency. N. Engl. J. Med,1967,276(21) :1163
  • 3Steffes MW. Schmidt D, McCrery R,et al. Glomerular cell number in normal subjects and in type Ⅰ diabetic patients. Kidney Int, 2001,59:2104
  • 4Pagtaluma ME, Miller PL, Jamping-Eagle S,et al. Podocyte loss and progressive glomerular injury in type Ⅱ diabetes. J Clin Invest, 1997, 90:342
  • 5MacDermot KD, Holmes A, Miners AH. Anderson-Fabry disease: clinical manifestations and impact of disease in a cohort of 98 hemizygous males. J Med Genet,2001,38 :750
  • 6Lao LM, Kumakiri M,Mima H,et al. The ultrastructural characteristics or eccrine sweat glands in a Fabry disease patient with hypohidrosis [J]. J Dermatol Sci,1998,18(2) :109
  • 7Syed NA,Sandbrink F, Luciano CA, et al. Cutaneous silent periods in patients with Fabry disease. Muscle Nerve ,2000,23,1179
  • 8Linhart A, Lubanda JC, Palecek T, et al. Cardiac manifestations in Fabry isease [J]. J Inherit Metab Dis, 2001,24 ( Suppl 2 ) :75
  • 9Sachdev B, Takenaka T, Teraguchi H, et al. Prevalence of AndersonFabry disease in male patients with late onset hypertrophic cardiomyopathy. Circulation ,2002,105:1407
  • 10Farge D,Nadlers,Wolfe LS,et al. Diagnostic value of kidney biopsy in heterozygous Fabry's disease. Arch Pathol Lab Med, 1985,109:85

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