个性化文献订阅>文章检索
  文章名  
  作者  
  期刊名  
  摘要  
   
   
   
  如果没有找到您所需要的文献,请点击 ——此处申请  
  共51条记录  
  • The clinical phenotype of Lynch syndrome due to germ-line PMS2 mutations
    [作者:Senter, L; Clendenning, M; Sotamaa, K; Hampel, H; Green, J; Potter, JD; Lindblom, A; Lagerstedt, K; Thibodeau, SN; Lindor, NM; Young, J; Winship, I; Dowty, JG; White, DM; Hopper, JL; Baglietto, L; Jenkins, MA; de la Chaple, A,期刊:Gastroenterology, 页码:419-428 , 文章类型: Article,,卷期:2008年135-2]
  • Background & Aims: Although the clinical phenotype of Lynch syndrome (also known as hereditary nonpolyposis colorectal cancer) has been well described, little is known about disease in PMS2 mutation carriers. Now that mu...
  • Identification of EpCAM as the gene for congenital tufting enteropathy
    [作者:Sivagnanam, M; Mueller, JL; Lee, H; Chen, Z; Nelson, SF; Turner, D; Zlotkin, SH; Pencharz, PB; Ngan, BY; Libiger, O; Schork, NJ; Lavine, JE; Taylor, S; Newbury, RO; Kolodner, RD; Hoffman, HM,期刊:Gastroenterology, 页码:429-437 , 文章类型: Article,,卷期:2008年135-2]
  • Background & Aims: Congenital tufting enteropathy (CTE) is a rare autosomal recessive diarrheal disorder presenting in the neonatal period. CTE is characterized by intestinal epithelial cell dysplasia leading to severe m...
  • Donor morbidity after living donation for liver transplantation
    [作者:Ghobrial, RM; Freise, CE; Trotter, JF; Tong, L; Ojo, AO; Fair, JH; Fisher, RA; Emond, JC; Koffron, AJ; Pruett, TL; Olthoff, KM,期刊:Gastroenterology, 页码:468-476 , 文章类型: Article,,卷期:2008年135-2]
  • Background & Aims: Reports of complications among adult right hepatic lobe donors have been limited to single centers. The rate and severity of complications in living donors were investigated in the 9-center Adult-to-Ad...
共51条记录 第一页 1 2 3 4 下一页 最后一页