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肾病综合征诊断进展 被引量:23

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作者 丁洁
出处 《中国实用儿科杂志》 CSCD 北大核心 2007年第6期401-403,共3页 Chinese Journal of Practical Pediatrics
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  • 1邓江红,丁洁,管娜,范青锋,张敬京.嘌呤霉素肾病大鼠肾小球足细胞相关分子表达的共定位分布[J].肾脏病与透析肾移植杂志,2004,13(3):205-210. 被引量:5
  • 2余自华,丁洁,黄建萍,姚勇,肖慧捷,张敬京,刘景城,杨霁云.散发性儿童激素耐药型肾病综合征NPHS2基因突变[J].中华肾脏病杂志,2004,20(6):413-417. 被引量:15
  • 3潘晓霞,陈楠,周伟,王朝晖,张文,王伟铭,陈晓农,巫永睿,陆颖.原发性局灶节段性肾小球硬化患者CD2AP基因突变的研究[J].中华肾脏病杂志,2006,22(1):13-18. 被引量:24
  • 4Weber S, Gribouval O, Esquivel EL, et al. NPHS2 mutation analysis shows genetic heterogeneity of steroid-resistant nephrotic syndrome and low post-transplant recurrence. Kidney Int, 2004,66 :571-579.
  • 5Caridi G, Berdeli A, Dagnino M, et al. Infantile steroid-resistantnephrotic syndrome associated with double homozygous mutations of podocin. Am J Kidney Dis, 2004, 43: 727-732.
  • 6Fuchshuber A, Jean G, Gribouval O, et al. Mapping a gene(SRNI) to chromosome 1q25-q31 in idiopathic nephrotic syndrome cortfirms a distinct entity of autosomal recessive nephrosis. Hum Mol Genet, 1995, 4 : 2155-2158.
  • 7Katie SM, Uetz B, Ronner V, et al. Novel mutations in NPHS2 detected in both familial and sporadic steroid-resistant nephrotic syndrome. J Am Sec Nephrol ,2002, 13: 388-393.
  • 8Caridi G, Bertelli R, C-arrea A, et al. Prevalence, genetics, and clinical features of patients carrying podocin mutations in steroidresistant nonfamilial focal segmental glomerulosclerosis. J Am Soc Nephrol ,2001, 12: 2742-2746.
  • 9Ruf RG, Lichtenberger A, Katie SM, et al. Patients with mutations in NPHS2 (podocin) do not respond to standard steroid treatment of nephrotic syndrome. J Am Soc Nephrol, 2004,15:722-732.
  • 10Boute N, Gribouval O, Roselli S, et al. NPHS2, encoding the glomerular protein podocin, is mutated in autosomal recessive steroidresistant nephrotic syndrome. Nat Genet, 2000, 24: 349-354.

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