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Volumn 25, Issue 2, 1997, Pages 224-227

Ovarian neoplasm and endometrioid carcinoma in a patient with Turcot syndrome

Author keywords

[No Author keywords available]

Indexed keywords

ANTINEOPLASTIC AGENT; FLUOROURACIL;

EID: 0030807046     PISSN: 02772116     EISSN: None     Source Type: Journal    
DOI: 10.1097/00005176-199708000-00018     Document Type: Article
Times cited : (3)

References (27)
  • 1
    • 0025890150 scopus 로고
    • Adenocarcinomas of the colon and rectum in persons under 40 years old
    • Griffin PM, Liff JM, Greenberg RS, et al. Adenocarcinomas of the colon and rectum in persons under 40 years old. Gastroenterology 1991;100:1033-40.
    • (1991) Gastroenterology , vol.100 , pp. 1033-1040
    • Griffin, P.M.1    Liff, J.M.2    Greenberg, R.S.3
  • 2
    • 0343441350 scopus 로고
    • Table 19B
    • Bethesda, MD: National Cancer Institute
    • Table 19B. In: National Cancer Institute Monograph. Bethesda, MD: National Cancer Institute, 1975;41:102.
    • (1975) National Cancer Institute Monograph , vol.41 , pp. 102
  • 3
    • 0343005747 scopus 로고
    • Tables 10A and 10D
    • Bethesda, MD: National Cancer Institute
    • Tables 10A and 10D. In: National Cancer Institute Monograph. Bethesda, MD: National Cancer Institute, 1981;57:1-187.
    • (1981) National Cancer Institute Monograph , vol.57 , pp. 1-187
  • 5
    • 0019202765 scopus 로고
    • Gardner's syndrome: Recent developments in research and management
    • Naylor EW, Lebenthal E. Gardner's syndrome: recent developments in research and management. Dig Dis Sci 1980;25:945-59.
    • (1980) Dig Dis Sci , vol.25 , pp. 945-959
    • Naylor, E.W.1    Lebenthal, E.2
  • 6
    • 0029164415 scopus 로고
    • In vitro transcription/translation assay for the screening of hMHL1 and hMSH2 mutations in familial colon cancer
    • Luce MC, Marra G, Chauhan DP, et al. In vitro transcription/translation assay for the screening of hMHL1 and hMSH2 mutations in familial colon cancer. Gastroenterology 1995;109:1368-74.
    • (1995) Gastroenterology , vol.109 , pp. 1368-1374
    • Luce, M.C.1    Marra, G.2    Chauhan, D.P.3
  • 7
    • 0029932906 scopus 로고    scopus 로고
    • Identification of DNA mismatch repair gene mutations in hereditary nonpolyposis colon cancer patients
    • Luce MC, Binnie CG, Cayouette MC, Kam-Morgan LNW. Identification of DNA mismatch repair gene mutations in hereditary nonpolyposis colon cancer patients. Int J Cancer 1996;69:50-2.
    • (1996) Int J Cancer , vol.69 , pp. 50-52
    • Luce, M.C.1    Binnie, C.G.2    Cayouette, M.C.3    Kam-Morgan, L.N.W.4
  • 9
    • 0023204649 scopus 로고
    • Recognition and treatment of patients with hereditary nonpolyposis colon cancer (Lynch syndromes I and II)
    • Fitzgibbons RJ, Lynch HT, Stanislav GV, et al. Recognition and treatment of patients with hereditary nonpolyposis colon cancer (Lynch syndromes I and II). Ann Surg 1987;206:289-95.
    • (1987) Ann Surg , vol.206 , pp. 289-295
    • Fitzgibbons, R.J.1    Lynch, H.T.2    Stanislav, G.V.3
  • 10
    • 0024243893 scopus 로고
    • Hereditary nonpolyposis colorectal cancer-Lynch syndromes I and II
    • Lynch HT, Lanspa SJ, Boman BM, et al. Hereditary nonpolyposis colorectal cancer-Lynch syndromes I and II. Gastroenterol Clin N Am 1988;17:679-711.
    • (1988) Gastroenterol Clin N Am , vol.17 , pp. 679-711
    • Lynch, H.T.1    Lanspa, S.J.2    Boman, B.M.3
  • 13
    • 0028970197 scopus 로고
    • The molecular basis of Turcot's syndrome
    • Hamilton SR, Liu B, Parsons RE, et al. The molecular basis of Turcot's syndrome. N Engl J Med 1995;332:839-47.
    • (1995) N Engl J Med , vol.332 , pp. 839-847
    • Hamilton, S.R.1    Liu, B.2    Parsons, R.E.3
  • 14
    • 0018356853 scopus 로고
    • Turcot's syndrome and its mode of inheritance
    • Itoh H, Ohsato K, Yao T, Iida M, Wantanabe H. Turcot's syndrome and its mode of inheritance. Gut 1979;20:414-9.
    • (1979) Gut , vol.20 , pp. 414-419
    • Itoh, H.1    Ohsato, K.2    Yao, T.3    Iida, M.4    Wantanabe, H.5
  • 16
    • 0025878474 scopus 로고
    • Multiple colorectal carcinomas, polyposis coli, and neurofibromatosis, followed by multiple glioblastoma multiforme
    • Pratt, CB. Multiple colorectal carcinomas, polyposis coli, and neurofibromatosis, followed by multiple glioblastoma multiforme. J Natl Cancer Inst 1991;83:880-1.
    • (1991) J Natl Cancer Inst , vol.83 , pp. 880-881
    • Pratt, C.B.1
  • 19
    • 0023141362 scopus 로고
    • Prevalence and importance of pigmented ocular fundus lesions in Gardner's syndrome
    • Traboulsi EI, Krush AJ, Gardner EJ, et al. Prevalence and importance of pigmented ocular fundus lesions in Gardner's syndrome. N Engl J Med 1987;316:661-67.
    • (1987) N Engl J Med , vol.316 , pp. 661-667
    • Traboulsi, E.I.1    Krush, A.J.2    Gardner, E.J.3
  • 20
    • 0027763498 scopus 로고
    • Molecular diagnosis of familial adenomatous polyposis
    • Powell SM, Petersen GM, Krush AJ, et al. Molecular diagnosis of familial adenomatous polyposis. N Engl J Med 1993;329:1982-7.
    • (1993) N Engl J Med , vol.329 , pp. 1982-1987
    • Powell, S.M.1    Petersen, G.M.2    Krush, A.J.3
  • 22
    • 0024843331 scopus 로고
    • High intensity basal ganglia lesions on Tl-weighted MR images in neurofibromatosis
    • Mirowitz SA, Sartor K, Gado M. High intensity basal ganglia lesions on Tl-weighted MR images in neurofibromatosis. AJNR 1990;10:1159-1163.
    • (1990) AJNR , vol.10 , pp. 1159-1163
    • Mirowitz, S.A.1    Sartor, K.2    Gado, M.3
  • 23
    • 0025337504 scopus 로고
    • Neurofibromatosis type-1 in childhood
    • Listernick R, Charrow J. Neurofibromatosis type-1 in childhood. J Pediatr 1990;116:845-52.
    • (1990) J Pediatr , vol.116 , pp. 845-852
    • Listernick, R.1    Charrow, J.2
  • 25
    • 0026505197 scopus 로고
    • Somatic mutations in the neurofibromatosis gene in human tumors
    • Li Y, Bollag G, Clark R, et al. Somatic mutations in the neurofibromatosis gene in human tumors. Cell 1992;69:275-81.
    • (1992) Cell , vol.69 , pp. 275-281
    • Li, Y.1    Bollag, G.2    Clark, R.3
  • 26
    • 0019755453 scopus 로고
    • Malignancy in neurofibromatosis
    • Hope DG, Mulvihill JJ. Malignancy in neurofibromatosis. Adv Neurology 1981;29:33-27.
    • (1981) Adv Neurology , vol.29 , pp. 33-127
    • Hope, D.G.1    Mulvihill, J.J.2
  • 27
    • 0029002475 scopus 로고
    • Distribution of 13 truncating mutations in the neurofibromatosis 1 gene
    • Heim RA, Kam-Morgan LNW, Binnie CG, et al. Distribution of 13 truncating mutations in the neurofibromatosis 1 gene. Hum Mol Genet 1995;4:975.
    • (1995) Hum Mol Genet , vol.4 , pp. 975
    • Heim, R.A.1    Kam-Morgan, L.N.W.2    Binnie, C.G.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.