| Te-Fu Tsai |
------>authors3_c=None ------>paper_class1=1 ------>Impact_Factor=None ------>paper_class3=1 ------>paper_class2=2 ------>vol=11 ------>confirm_bywho=lm ------>insert_bywho=tis ------>Jurnal_Rank=None ------>authors4_c=None ------>comm_author=1 ------>patent_EDate=None ------>authors5_c=None ------>publish_day=13 ------>paper_class2Letter=None ------>page2=133 ------>medlineContent= ------>unit=E0117 ------>insert_date=20060216 ------>iam=2 ------>update_date=None ------>author=??? ------>change_event=4 ------>ISSN= ------>authors_c=None ------>score=244 ------>journal_name=J Urol R.O.C. ------>paper_name=Multilocular Cystic Nephroma: A case report and literature review ------>confirm_date=20060426 ------>tch_id=092077 ------>pmid=14626682 ------>page1=131 ------>fullAbstract=We present a new case of multilocular cystic nephroma, and a review of literature. If C.T. diagnoses a cystic disease we apply the Bosniak classification. Multilocular cystic nephroma appears as a cystic disease, separately fibrous thin walls, with or without calcifications. We have to make a distinctive diagnosis between RCC and multilocular. Definitive diagnosis is always histological. ------>tmu_sno=None ------>sno=12909 ------>authors2=Thomas I.S. Hwang ------>authors3= ------>authors4= ------>authors5= ------>authors6= ------>authors6_c=None ------>authors=Te-Fu Tsai ------>delete_flag=0 ------>SCI_JNo=None ------>authors2_c=None ------>publish_area=0 ------>updateTitle=[Cystic multilocular nephroma. Report of a case] ------>language=2 ------>check_flag=None ------>submit_date=None ------>country=None ------>no=3 ------>patent_SDate=None ------>update_bywho=None ------>publish_year=2000 ------>submit_flag=None ------>publish_month=12 |