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黑斑息肉综合征诊治进展 被引量:3

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作者 孙淑卿
出处 《医学文选》 2001年第1期78-80,共3页 Anthology of Medicine
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参考文献19

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  • 3刘汶.Peutz-Jeghers综合征[J].中华外科杂志,1984,22(9):570-570.
  • 4Hemminki A,Markie D,Tomlinson I,et al.A serine/threonine kinase gene defective inPeutz-Jeghers syndrome.Nature,1998,391:184~187
  • 5Jenne DE,Reimann H,Nezu J,et al.Peutz-Jeghers syndrome is caused by mutations in anovel serine threonine kinase.Nature Genetics,1988,18:38~43
  • 6王振军,严仲瑜,毕郭龙,徐文怀,黄莚庭.国人黑斑息肉病LKB1基因胚系突变的检测[J].中华外科杂志,2000,38(2):104-105. 被引量:18
  • 7康连春,张家芳,郭凌,范登华,张士华,何晓蕴.消化道多发性息肉综合征[J].中华消化杂志,1997,17(2):79-81. 被引量:11
  • 8殷广福 郑志同 李祥周.黑色斑点—肠道多发息肉综合征一例[J].天津医药,1986,14(9):568-569.
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二级参考文献8

  • 1江绍基,临床胃肠病学,1981年,627页
  • 2团体著者,内科疾病鉴别诊断学,1975年,671页
  • 3隋建超,新消化病学杂志,1995年,1卷,53页
  • 4汤钊猷,现代肿瘤学,1993年,44页
  • 5刘国瑞,人类遗传病学(译),1990年,668,205页
  • 6武忠弼,病理学总论与各论(译),1989年,10,129页
  • 7Wang Z J,Am J Pathol,1998年,153卷,363页
  • 8Hidewaki Nakagawa,Kumiko Koyama,Toshihiro Tanaka,Yasuo Miyoshi,Hiroshi Ando,Shozo Baba,Masahiro Watatani,Masayuki Yasutomi,Morito Monden,Yusuke Nakamura. Localization of the gene responsible for Peutz-Jeghers syndrome within a 6-cM region of chromosome 19p13.3[J] 1998,Human Genetics(2):203~206

共引文献37

同被引文献23

  • 1[2]Leggett BA,Young JP,Barker M.Peutz-Jeghers syndrome:genetic screening[J].Expert Rev Anticancer Ther,2003,3(4):518-24.
  • 2[3]Giardiello FM,Brensinger JD,Tersmette AC,et al.Very high risk of cancer in familial Peutz-Jeghers syndrome [J].Gastroenterology,2000,119(6):1447-453.
  • 3[5]Hemminki A,Markie D,Tomlinson I,et al.A serine/threnine kinase gene defective in Peutz-Jeghers syndrome [J].Nature,1998,391:184-87.
  • 4[6]Jenne DE,Reimann H,Nezu J,et al.Peutz-Jeghers syndrome is caused by mutations in novel serine threonine kinase [J].Nat Genet,1988,18:38-43.
  • 5[8]Keshtgar AS,Losty PD,Lloyd DA,et al.Recent developments in the management of Peutz-Jeghers syndrome in childhood [J].Eur J Pediatr Surg,1997,7(6):367-68.
  • 6殷广福 郑志同 李祥周.黑色斑点—肠道多发息肉综合征一例[J].天津医药,1986,14(9):568-569.
  • 7Butt R W. Poloyposis syndromes[ J]. Clin Perspect Crastrol, 2002, 2 (1): 51.
  • 8Foley TR, Mc Garrity TJ, Abt AB, et al. Peutz-Jeghers syndrome: a clinicopathologic survey of the "Harrisburg family" with a 49oyear follow-up[J]. Gastroenterology, 1988, 95(6): 1535-40.
  • 9Wang ZJ, Ellis I, Zauber P, et al. Allelic imbalance at the LKB1 (STK11) locus in tumors from patients with Peutz-Jeghers' syndrome provides evidence for a hamartoma-(adenoma)-carcinoma sequence[J]. J Pathol, 1999, 188(1): 9-13.
  • 10Taguchi T, Suita S, Taguchi S, et al. Peutz-Jeghers syndrome in children: high recurrence rate in short-term follow-up [J]. Asian J Surg, 2003, 26(4): 221-4.

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二级引证文献16

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