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胃食管外阴平滑肌瘤病1例 被引量:3

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作者 刘晨 祝亚猛
出处 《中国妇产科临床杂志》 2006年第4期294-295,共2页 Chinese Journal of Clinical Obstetrics and Gynecology
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参考文献8

  • 1[2]Wahlen T,Astedt B.Familial occurrence of coexisting leiomyoma of vulva and esophagus.Acta Obstet Gynecol Scand,1965,44:197-203.
  • 2[3]Siegler RW,Rothstein RI,Beecham JB,et al.Gastroesophageal-Vulvar leiomyomatosis presenting over the course of 20 years.Arch Pathol Lab Med,1996,120:1141-1144.
  • 3[4]Compagnoni G,Talamonti M,Joob A,et al.Esophageal leiomyomatosis in a woman with a history of vulvar leiomyoma and Barrett's Esophagus.DigSurg,2000,17:306-309.
  • 4[5]Faber K,Jones MA,Spratt D,et al.Vulvar leiomyomatosis in a patient with esophagogastric leiomyomatosis:review of the syndrome.Gynecol Oncol,1991,41:92-94.
  • 5[6]Tavasolli FA,Norris HI.Smooth muscle tumors of the vulva.Obstet Gynecol,1997,53:213-217.
  • 6[7]Garcia Torres R,Guarner V.Leiomyomatosis of the esophagus,tracheobronchi and genitals associated with Alport type hereditary nephropathy:a new syndrome.Rev Gastroenterol Mex,1983,48:163-170.
  • 7[8]Zhou J,Mochizuki T,Srneets H,et al.Deletion of the pairedα5 (Ⅳ)andα6 (Ⅳ) collagen genes in inherited smooth muscle tumors.Science,1993,261:1167-1168.
  • 8王芳,丁洁,俞礼霞,杨霁云.伴食管平滑肌瘤的Alport综合征基因突变特征[J].肾脏病与透析肾移植杂志,2003,12(3):207-210. 被引量:11

二级参考文献17

  • 1丁洁,杨霁云,刘景城,俞礼霞.免疫荧光学方法检查皮肤组织Ⅳ型胶原α5链诊断Alport综合征[J].中华儿科杂志,1997,35(4):177-179. 被引量:33
  • 2Kashtan CE. Familial hematuric syndromes-Alport syndrome, Thin glomerular basement membrane disease and Fechrner/Epstein syndromes. Contrib Nephrol. Basel, Karger,2001,136:pp79.
  • 3Pirson Y. Making the diagnosis of Alport's syndrome. Kidney Int, 1999, 56:760.
  • 4Jais JP, Knebelmann B, Giatms I, et al. X-linked Alport syndrome: Natural history in 195 families and genotype-phentotype correlations in males. J Am Soc Nephrol, 2000, 11:649.
  • 5Pajari H, Setala K, Heiskari N, et al. Ocular findings in 34 patients with Alport syndrome: correlation of the rindings to mutations in COL4A5 gene. Acta Ophthalmol Scand, 1999, 77:214.
  • 6Antignae C, Heidet L. Mutations in Alport syndrome associated with diffuse esophageal leiomyomatosis. Contrib Nephrol. Basel, Kazger, 1996, 117:pp172.
  • 7Zhou J, Mochizuki T, Smeets H, et al. Deletion of the paired α5(Ⅳ) and α6( Ⅳ ) collagen genes in inherited smooth muscle tumors. Science, 1993, 261:1 167.
  • 8Lemmink HH, Schroder CH, Monnens LAH, et al. The clinical spectrum of type Ⅳ collagen mutations. Hum Murat, 1997,9:477.
  • 9Heidet L, Cohen-Solal L, Boye E, et al. Novel COL4A5/COL4A6 deletions and further characterization of the diffuse leiomyomatosis-Alport syndrome (DL-AS) locus define the DL critical region. Cyogenet Cell Genet, 1997,78:240.
  • 10Mothes H, Heidet L, Arrondel C, et al. Alport syndrome associated with diffuse leiomyomatosis: COL4A5-COL4A6 deletion associated with a mild form of Alport nephropathy. Nephrol Dial Transplant,2002,17:70.

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