메뉴 건너뛰기




Volumn 105, Issue 41, 2008, Pages 706-714

Hereditary cancer syndromes;Erbliche krebserkrankungen

Author keywords

Cancer syndromes; Genetic counseling; Molecular genetic diagnostics; Monogenic diseases; Surveillance

Indexed keywords

ARTICLE; BREAST CANCER; CLINICAL FEATURE; COLORECTAL CANCER; FAMILIAL CANCER; FAMILIAL POLYPOSIS; GENE MUTATION; GENETIC COUNSELING; HUMAN; MULTIPLE CANCER; OVARY CANCER; PERIODIC MEDICAL EXAMINATION; PRACTICE GUIDELINE; PRIMARY MEDICAL CARE; SIPPLE SYNDROME;

EID: 56349083346     PISSN: 00121207     EISSN: None     Source Type: Journal    
DOI: 10.3238/arztebl.2008.0706     Document Type: Article
Times cited : (67)

References (25)
  • 2
    • 56349142905 scopus 로고    scopus 로고
    • Richtlinien zur Diagnostik der genetischen Disposition für Krebserkrankungen. Dtsch Arztebl 1998; 95(22): A 1396.
    • Richtlinien zur Diagnostik der genetischen Disposition für Krebserkrankungen. Dtsch Arztebl 1998; 95(22): A 1396.
  • 3
    • 0035522894 scopus 로고    scopus 로고
    • Two genetic hits (more or less) to cancer
    • Knudson AG: Two genetic hits (more or less) to cancer. Nat Rev Cancer 2001; 1: 157-62.
    • (2001) Nat Rev Cancer , vol.1 , pp. 157-162
    • Knudson, A.G.1
  • 4
    • 33750085341 scopus 로고    scopus 로고
    • Indikationen zur molekulargenetischen Diagnostik bei erblichen Krankheiten.
    • A 550-8
    • Aretz S, Propping P, Nöthen MM: Indikationen zur molekulargenetischen Diagnostik bei erblichen Krankheiten. Dtsch Arztebl 2006; 103(9): A 550-8.
    • (2006) Dtsch Arztebl , vol.103 , Issue.9
    • Aretz, S.1    Propping, P.2    Nöthen, M.M.3
  • 5
    • 0035865285 scopus 로고    scopus 로고
    • Effectiveness of breast cancer surveillance in BRCA1/2 gene mutation carriers and women with high familial risk
    • Brekelmans CT, Seynaeve C, Bartels CC et al.: Effectiveness of breast cancer surveillance in BRCA1/2 gene mutation carriers and women with high familial risk. J Clin Oncol. 2001; 19: 924-30.
    • (2001) J Clin Oncol , vol.19 , pp. 924-930
    • Brekelmans, C.T.1    Seynaeve, C.2    Bartels, C.C.3
  • 6
    • 42549165647 scopus 로고    scopus 로고
    • Guidelines for the clinical management of familial adenomatous polyposis (FAP)
    • Vasen HF, Möslein G, Alonso A et al.: Guidelines for the clinical management of familial adenomatous polyposis (FAP). Gut 2008; 57: 704-13.
    • (2008) Gut , vol.57 , pp. 704-713
    • Vasen, H.F.1    Möslein, G.2    Alonso, A.3
  • 7
    • 56349147314 scopus 로고    scopus 로고
    • Krebs in Deutschland 2003-2004. Häufigkeiten und Trends. 6. überarbeitete Auflage. Robert Koch-Institut (Hrsg.) und die Gesellschaft der epidemiologischen Krebsregister in Deutschland e.V. (Hrsg.). Berlin, 2008.
    • Krebs in Deutschland 2003-2004. Häufigkeiten und Trends. 6. überarbeitete Auflage. Robert Koch-Institut (Hrsg.) und die Gesellschaft der epidemiologischen Krebsregister in Deutschland e.V. (Hrsg.). Berlin, 2008.
  • 9
    • 0033063711 scopus 로고    scopus 로고
    • New clinical criteria for hereditary nonpolyposis colorectal cancer (HNPCC, Lynch syndrome) proposed by the International Collaborative group on HNPCC
    • Vasen HF, Watson P, Mecklin JP, Lynch HT: New clinical criteria for hereditary nonpolyposis colorectal cancer (HNPCC, Lynch syndrome) proposed by the International Collaborative group on HNPCC. Gastroenterology 1999; 116: 1453-6.
    • (1999) Gastroenterology , vol.116 , pp. 1453-1456
    • Vasen, H.F.1    Watson, P.2    Mecklin, J.P.3    Lynch, H.T.4
  • 10
    • 33751501011 scopus 로고    scopus 로고
    • Frequency of hereditary non-polyposis colorectal cancer among unselected patients with colorectal cancer in Germany
    • Lamberti C, Mangold E, Pagenstecher C et al.: Frequency of hereditary non-polyposis colorectal cancer among unselected patients with colorectal cancer in Germany. Digestion. 2006; 74: 58-67.
    • (2006) Digestion , vol.74 , pp. 58-67
    • Lamberti, C.1    Mangold, E.2    Pagenstecher, C.3
  • 11
    • 10744233937 scopus 로고    scopus 로고
    • Revised Bethesda Guidelines for hereditary nonpolyposis colorectal cancer (Lynch syndrome) and microsatellite instability
    • Umar A, Boland CR, Terdiman JP et al.: Revised Bethesda Guidelines for hereditary nonpolyposis colorectal cancer (Lynch syndrome) and microsatellite instability. J Natl Cancer Inst 2004; 96: 261-8.
    • (2004) J Natl Cancer Inst , vol.96 , pp. 261-268
    • Umar, A.1    Boland, C.R.2    Terdiman, J.P.3
  • 12
    • 0031551963 scopus 로고    scopus 로고
    • A National Cancer Institute Workshop on Hereditary Nonpolyposis Colorectal Cancer Syndrome: Meeting highlights and Bethesda guidelines
    • Rodriguez-Bigas MA, Boland CR, Hamilton SR et al.: A National Cancer Institute Workshop on Hereditary Nonpolyposis Colorectal Cancer Syndrome: meeting highlights and Bethesda guidelines. J Natl Cancer Inst 1997. 3; 89: 1758-62.
    • (1997) J Natl Cancer Inst , vol.3 , Issue.89 , pp. 1758-1762
    • Rodriguez-Bigas, M.A.1    Boland, C.R.2    Hamilton, S.R.3
  • 13
    • 13244282497 scopus 로고    scopus 로고
    • Wirksamkeit der Krebsfrüherkennung beim hereditären kolorektalen Karzinom ohne Polyposis.
    • A 506-12
    • Schulmann K, Mangold E, Schmiegel W, Propping P: Wirksamkeit der Krebsfrüherkennung beim hereditären kolorektalen Karzinom ohne Polyposis. Dtsch Arztebl 2004; 101(8): A 506-12.
    • (2004) Dtsch Arztebl , vol.101 , Issue.8
    • Schulmann, K.1    Mangold, E.2    Schmiegel, W.3    Propping, P.4
  • 14
    • 42049105190 scopus 로고    scopus 로고
    • Familiäre adenomatöse Polyposis
    • Ganten D, Ruckpaul K Hrsg, Springer, Berlin, Heidelberg, New York
    • Friedl W, Lamberti C: Familiäre adenomatöse Polyposis. In: Ganten D, Ruckpaul K (Hrsg). Hereditäre Tumorerkrankungen. Springer, Berlin, Heidelberg, New York, 2001; 305-29.
    • (2001) Hereditäre Tumorerkrankungen , pp. 305-329
    • Friedl, W.1    Lamberti, C.2
  • 16
    • 0027731797 scopus 로고
    • Prevention of colorectal cancer by colonoscopic polypectomy. The National Polyp Study Workgroup
    • Winawer SJ, Zauber AG, Ho MN et al.: Prevention of colorectal cancer by colonoscopic polypectomy. The National Polyp Study Workgroup. N Engl J Med 1993; 329: 1977-81.
    • (1993) N Engl J Med , vol.329 , pp. 1977-1981
    • Winawer, S.J.1    Zauber, A.G.2    Ho, M.N.3
  • 17
    • 33745903402 scopus 로고    scopus 로고
    • MUTYH-associated polyposis: 70 of 71 patients with biallelic mutations present with an attenuated or atypical phenotype
    • Aretz S, Uhlhaas S, Goergens H et al.: MUTYH-associated polyposis: 70 of 71 patients with biallelic mutations present with an attenuated or atypical phenotype. Int J Cancer 2006; 119: 807-14.
    • (2006) Int J Cancer , vol.119 , pp. 807-814
    • Aretz, S.1    Uhlhaas, S.2    Goergens, H.3
  • 19
    • 56349116186 scopus 로고    scopus 로고
    • Schmutzler R, Schlegelberger B, Meindl A et al.: Hereditäre Brustkrebserkrankung. In: Stufe-3-Leitlinie Brustkrebs-Früherkennung in Deutschland, 1. Aktualisierung 2008, Herausgeberin U.-S. Albert für die Mitglieder der Planungsgruppe und Leiter der Arbeitsgruppen Konzertierte Aktion Brustkrebs-Früherkennung in Deutschland. Zuckerschwerdt Verlag: München, Wien, New York, 2008; 56-9.
    • Schmutzler R, Schlegelberger B, Meindl A et al.: Hereditäre Brustkrebserkrankung. In: Stufe-3-Leitlinie Brustkrebs-Früherkennung in Deutschland, 1. Aktualisierung 2008, Herausgeberin U.-S. Albert für die Mitglieder der Planungsgruppe und Leiter der Arbeitsgruppen Konzertierte Aktion Brustkrebs-Früherkennung in Deutschland. Zuckerschwerdt Verlag: München, Wien, New York, 2008; 56-9.
  • 20
    • 0034936364 scopus 로고    scopus 로고
    • Evidence for further breast cancer susceptibility genes in addition to BRCA1 and BRCA2 in a population-based study
    • Antoniou AC, Pharoah PD, McMullan G, Day NE, Ponder BA, Easton D: Evidence for further breast cancer susceptibility genes in addition to BRCA1 and BRCA2 in a population-based study. Genet Epidemiol 2001; 21: 1-18.
    • (2001) Genet Epidemiol , vol.21 , pp. 1-18
    • Antoniou, A.C.1    Pharoah, P.D.2    McMullan, G.3    Day, N.E.4    Ponder, B.A.5    Easton, D.6
  • 21
    • 33645084562 scopus 로고    scopus 로고
    • Spectrum of mutations in BRCA1, BRCA2, CHEK2, and TP53 in families at high risk of breast cancer
    • Walsh T, Casadei S, Coats KH: Spectrum of mutations in BRCA1, BRCA2, CHEK2, and TP53 in families at high risk of breast cancer. JAMA 2006; 22; 295: 1379-88.
    • (2006) JAMA , vol.22 , Issue.295 , pp. 1379-1388
    • Walsh, T.1    Casadei, S.2    Coats, K.H.3
  • 22
    • 34248191961 scopus 로고    scopus 로고
    • Marini F, Falchetti A, Del Monte F et al.: Multiple endocrine neoplasia type 2. Orphanet J Rare Dis 2006; 1: 45.
    • Marini F, Falchetti A, Del Monte F et al.: Multiple endocrine neoplasia type 2. Orphanet J Rare Dis 2006; 1: 45.
  • 23
    • 56349170192 scopus 로고    scopus 로고
    • Multiple endokrine Neoplasie
    • Ganten D, Ruckpaul K Hrsg, Springer: Berlin, Heidelberg, New York
    • Ritter MM, Höppner W: Multiple endokrine Neoplasie. In: Ganten D, Ruckpaul K (Hrsg). Hereditäre Tumorerkrankungen. Springer: Berlin, Heidelberg, New York, 2001, 430.
    • (2001) Hereditäre Tumorerkrankungen , pp. 430
    • Ritter, M.M.1    Höppner, W.2
  • 24
    • 0028896366 scopus 로고
    • ARCAD: A method for estimating age-dependent disease risk associated with mutation carrier status from family data
    • Le Bihan C, Moutou C, Brugieres L, Feunteun J, Bonaiti-Pellie C: ARCAD: a method for estimating age-dependent disease risk associated with mutation carrier status from family data. Genet Epidemiol 1995; 12: 13-25.
    • (1995) Genet Epidemiol , vol.12 , pp. 13-25
    • Le Bihan, C.1    Moutou, C.2    Brugieres, L.3    Feunteun, J.4    Bonaiti-Pellie, C.5
  • 25
    • 1642457364 scopus 로고    scopus 로고
    • Recognition and management of hereditary breast cancer syndromes
    • Thull DL, Vogel VG: Recognition and management of hereditary breast cancer syndromes. Oncologist 2004; 9: 13-24.
    • (2004) Oncologist , vol.9 , pp. 13-24
    • Thull, D.L.1    Vogel, V.G.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.