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    1. Ricevuto, E; Sobol, H; Stoppa-Lyonnet, D; Gulino, A; Marchetti, P; Ficorella, C; Martinotti, S; Meo, T; Tosi, M
      Diagnostic strategy for analytical scanning of BRCA1 gene by fluorescence-assisted mismatch analysis using large, bifluorescently labeled amplicons

      CLINICAL CANCER RESEARCH
    2. Gad, S; Aurias, A; Puget, N; Mairal, A; Schurra, C; Montagna, M; Pages, S; Caux, V; Mazoyer, S; Bensimon, A; Stoppa-Lyonnet, D
      Color bar coding the BRCAI gene on combed DNA: A useful strategy for detecting large gene rearrangements

      GENES CHROMOSOMES & CANCER
    3. Lefevre, SH; Vogt, N; Dutrillaux, AM; Chauveinc, K; Stoppa-Lyonnet, D; Doz, F; Desjardins, L; Dutrillaux, B; Chevillard, S; Malfoy, B
      Genome instability in secondary solid tumors developing after radiotherapyof bilateral retinoblastoma

      ONCOGENE
    4. Gad, S; Stoppa-Lyonnet, D; Aurias, A; Bensimon, A
      Colour bar coding on combed DNA revealed large gene rearrangements of BRCA1 gene

      M S-MEDECINE SCIENCES
    5. Gad, S; Scheuner, MT; Pages-Berhouet, S; Caux-Moncoutier, V; Bensimon, A; Aurias, A; Pinto, M; Stoppa-Lyonnet, D
      Identification of a large rearrangement of the BRCA1 gene using colour barcode on combed DNA in an American breast/ovarian cancer family previously studied by direct sequencing

      JOURNAL OF MEDICAL GENETICS
    6. Bougeard, G; Limacher, JM; Martin, C; Charbonnier, F; Killian, A; Delattre, O; Longy, M; Jonveaux, P; Fricker, JP; Stoppa-Lyonnet, D; Flaman, JM; Frebourg, T
      Detection of 11 germline inactivating TP53 mutations and absence of TP63 and HCHK2 mutations in 17 French families with Li-Fraumeni or Li-Fraumeni-like syndrome

      JOURNAL OF MEDICAL GENETICS
    7. Chompret, A; Abel, A; Stoppa-Lyonnet, D; Brugieres, L; Pages, S; Feunteun, J; Bonaiti-Pellie, C
      Sensitivity and predictive value of criteria for p53 germline mutation screening

      JOURNAL OF MEDICAL GENETICS
    8. Geoffroy-Perez, B; Janin, N; Ossian, K; Lauge, A; Croquette, MF; Griscelli, C; Debre, M; Bressac-De-Paillerets, B; Aurias, A; Stoppa-Lyonnet, D; Andrieu, N
      Cancer risk in heterozygotes for ataxia-telangiectasia

      INTERNATIONAL JOURNAL OF CANCER
    9. Frebourg, T; Ebel, A; Bonaiti-Pellie, C; Brugieres, L; Berthet, P; Bressac-De Paillerets, B; Chevrier, A; Chompret, A; Cohen-Haguenauer, O; Delattre, O; Feingold, J; Feunteun, J; Frappaz, D; Fricker, JP; Gesta, P; Jonveaux, P; Kalifa, C; Lasset, C; Leheup, B; Limacher, JM; Longy, M; Nogues, C; Oppenheim, D; Sommelet, D; Soubrier, F; Stoll, C; Stoppa-Lyonnet, D; Tristant, H
      Li-Fraumeni syndrome: update, new data and guidelines for clinical management

      BULLETIN DU CANCER
    10. Pages, S; Caux, V; Stoppa-Lyonnet, D; Tosi, M
      Screening of male breast cancer and of breast-ovarian cancer families for BRCA2 mutations using large bifluorescent amplicons

      BRITISH JOURNAL OF CANCER
    11. Lakhani, SR; Gusterson, BA; Jacquemier, J; Sloane, JP; Anderson, TJ; van de Vijver, MJ; Venter, D; Freeman, A; Antoniou, A; McGuffog, L; Smyth, E; Steel, CM; Haites, N; Scott, RJ; Goldgar, D; Neuhausen, S; Daly, PA; Ormiston, W; McManus, R; Scherneck, S; Ponder, BAJ; Futreal, PA; Peto, J; Stoppa-Lyonnet, D; Bignon, YJ; Struewing, JP; Bishop, DT; Klijn, JGM; Devilee, P; Cornelisse, CJ; Lasset, C; Lenoir, G; Barkardottir, RB; Egilsson, V; Hamann, U; Chang-Claude, J; Sobol, H; Weber, B; Easton, DF; Stratton, MR
      The pathology of familial breast cancer: Histological features of cancers in families not attributable to mutations in BRCA1 or BRCA2

      CLINICAL CANCER RESEARCH
    12. Stoppa-Lyonnet, D; Ansquer, Y; Dreyfus, H; Gautier, C; Gauthier-Villars, M; Bourstyn, E; Clough, KB; Magdelenat, H; Pouillart, P; Vincent-Salomon, A; Fourquet, A; Asselain, B
      Familial invasive breast cancers: Worse outcome related to BRCA1 mutations

      JOURNAL OF CLINICAL ONCOLOGY
    13. Julian-Reynier, C; Eisinger, F; Chabal, F; Lasset, C; Nogues, C; Stoppa-Lyonnet, D; Vennin, P; Sobol, H
      Disclosure to the family of breast/ovarian cancer genetic test results: Patient's willingness and associated factors

      AMERICAN JOURNAL OF MEDICAL GENETICS
    14. Narod, SA; Brunet, JS; Ghadirian, P; Robson, M; Heimdal, K; Neuhausen, SL; Stoppa-Lyonnet, D; Lerman, C; Pasini, B; de los Rios, P; Weber, B; Lynch, H
      Tamoxifen and risk of contralateral breast cancer in BRCA1 and BRCA2 mutation carriers: a case-control study

      LANCET
    15. Eisinger, F; Julian-Reynier, C; Stoppa-Lyonnet, D; Lasset, C; Nogues, C
      Acceptability of prophylactic mastectomy in cancer-prone women

      JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION
    16. Hodgson, SV; Haites, NE; Caligo, M; Chang-Claude, J; Eccles, D; Evans, G; Moller, P; Morrison, P; Steel, CM; Stoppa-Lyonnet, D; Vasen, H
      A survey of the current clinical facilities for the management of familialcancer in Europe

      JOURNAL OF MEDICAL GENETICS
    17. Bay, JO; Uhrhammer, N; Stoppa-Lyonnet, D; Hall, J
      Role of the ATM gene in genetic predisposition to cancer

      BULLETIN DU CANCER
    18. Freneaux, P; Stoppa-Lyonnet, D; Mouret, E; Kambouchner, M; Nicolas, A; Zafrani, B; Vincent-Salomon, A; Fourquet, A; Magdelenat, H; Sastre-Garau, X
      Low expression of bcl-2 in Brca1-associated breast cancers

      BRITISH JOURNAL OF CANCER
    19. Soufir, N; Bressac-de Paillerets, B; Desjardins, L; Levy, C; Bombled, J; Gorin, I; Schlienger, P; Stoppa-Lyonnet, D
      Individuals with presumably hereditary uveal melanoma do not harbour germline mutations in the coding regions of either the P16(INK4A), P14(ARF) or cdk4 genes

      BRITISH JOURNAL OF CANCER
    20. Stoppa-Lyonnet, D; Lauge, A; Sigaux, F; Stern, MH
      No germline ATM mutation in a series of 16 T-cell prolymphocytic leukemias

      BLOOD
    21. Mazoyer, S; Leary, J; Kirk, J; Fleischmann, E; Wagner, T; Claes, K; Messiaen, L; Foulkes, W; Desrochers, M; Simard, J; Phelan, CM; Kwan, E; Narod, SA; Vahteristo, P; Nevanlinna, H; Durando, X; Bignon, YJ; Peyrat, JP; Bonnardel, C; Sinilnikova, OM; Puget, N; Lenoir, GM; Mazoyer, S; Audoynaud, C; Goldgar, D; Maugard, C; Caux, V; Gad, S; Stoppa-Lyonnet, D; Nogues, C; Lidereau, R; Machavoine, C; Bressac-de Paillerets, B; Kuschel, B; Betz, B; Niederacher, D; Beckmann, MW; Hamann, U; Gayther, SA; Ponder, BAP; Robinson, M; Taylor, GR; Bishop, T; Catteau, A; Solomon, E; Cohen, B; Steel, M; Collins, N; Stratton, M; van der Looij, M; Olah, E; Miller, NJ; Barton, DE; Sverdlov, RS; Friedman, E; Radice, P; Montagna, M; Sensi, E; Caligo, M; van Eijk, R; Devilee, P; van der Luijt, R; Heimdal, K; Moller, P; Borg, A; Diez, O; Cortes, J; Domenech, M; Baiget, M; Osorio, A; Benitez, J; Borg, A; Maillet, P; Sappino, AP; Ozdag, H; Ozcelik, T; Ozturk, M; Rohlfs, EM; Boyd, J; McDermott, D; Offit, K; Unger, M; Nathanson, K; Weber, BL; Sellers, TA; Hampton, E; Couch, FJ; Neuhausen, S
      The exon 13 duplication in the BRCA1 gene is a founder mutation present ingeographically diverse populations

      AMERICAN JOURNAL OF HUMAN GENETICS
    22. Wagner, T; Stoppa-Lyonnet, D; Fleischmann, E; Muhr, D; Pages, S; Sandberg, T; Caux, V; Moeslinger, R; Langbauer, G; Borg, A; Oefner, P
      Denaturing high-performance liquid chromatography detects reliably BRCA1 and BRCA2 mutations

      GENOMICS
    23. Bay, JO; Uhrhammer, N; Hall, J; Stoppa-Lyonnet, D; Bignon, YJ
      ATM functions and ataxia-telangectasia phenotypes

      M S-MEDECINE SCIENCES
    24. Hodgson, S; Milner, B; Brown, I; Bevilacqua, G; Chang-Claude, J; Eccles, D; Evans, G; Gregory, H; Moller, P; Morrison, P; Steel, M; Stoppa-Lyonnet, D; Vasen, H; Haites, N
      Cancer genetics services in Europe

      DISEASE MARKERS
    25. Sobol, H; Bignon, YJ; Bonaiti, C; Cuisenier, J; Lasset, C; Lortholary, A; Nogues, C; Stoppa-Lyonnet, D; Eisinger, F
      Four years analysis of cancer genetic clinics activity in France from 1994to 1997: A survey on 801 patients

      DISEASE MARKERS
    26. Vasen, HFA; Haites, NE; Evans, DGR; Steel, CM; Moller, P; Hodgson, S; Eccles, D; Morrison, P; Stoppa-Lyonnet, D; Chang-Claude, J; Caligo, M
      Current policies for surveillance and management in women at risk for breast and ovarian cancer: A survey among 16 European family cancer clinics

      DISEASE MARKERS
    27. Chang-Claude, J; Becher, H; Caligo, M; Eccles, D; Evans, G; Haites, N; Hodgson, S; Moller, P; Weber, BHF; Stoppa-Lyonnet, D
      Risk estimation as a decision-making tool for genetic analysis of the breast cancer susceptibility genes

      DISEASE MARKERS
    28. Stoppa-Lyonnet, D; Caligo, M; Eccles, D; Evans, DGR; Haites, NE; Hodgson, NS; Moller, P; Morrison, PJ; Steel, CM; Vasen, HFA; Chang-Claude, J
      Genetic testing for breast cancer predisposition in 1999: which molecular strategy and which family criteria?

      DISEASE MARKERS
    29. Steel, M; Smyth, E; Vasen, H; Eccles, D; Evans, G; Moller, P; Hodgson, S; Stoppa-Lyonnet, D; Chang-Claude, J; Caligo, M; Morrison, P; Haites, N
      Ethical, social and economic issues in familial breast cancer: a compilation of views from the EC biomed II demonstration project

      DISEASE MARKERS
    30. Evans, DGR; Anderson, E; Lalloo, F; Vasen, H; Beckmann, M; Eccles, D; Hodgson, S; Moller, P; Chang-Claude, J; Morrison, P; Stoppa-Lyonnet, D; Steel, M; Haites, N
      Utilisation of prophylactic mastectomy in 10 European centers

      DISEASE MARKERS
    31. Morrison, PJ; Steel, CM; Vasen, HFA; Eccles, D; Evans, DGR; Moller, P; Hodgson, S; Stoppa-Lyonnet, D; Chang-Claude, J; Caligo, M; Olah, E; Haites, NE; Nevin, NC
      Insurance implications for individuals with a high risk of breast and ovarian cancer in Europe

      DISEASE MARKERS
    32. Moller, P; Evans, G; Haites, N; Vasen, H; Reis, MM; Anderson, E; Apold, J; Hodgson, S; Eccles, D; Olsson, H; Stoppa-Lyonnet, D; Chang-Claude, J; Morrison, PJ; Bevilacqua, G; Heimdal, K; Maehle, L; Lalloo, F; Gregory, H; Preece, P; Borg, A; Nevin, NC; Caligo, M; Steel, CM
      Guidelines for follow-up of women at high risk for inherited breast cancer: Consensus statement from the Biomed 2 Demonstration Programme on Inherited Breast Cancer

      DISEASE MARKERS
    33. Gauthier-Villars, M; Gad, S; Caux, V; Pages, S; Blandy, C; Stoppa-Lyonnet, D
      Genetic testing for breast cancer predisposition

      SURGICAL CLINICS OF NORTH AMERICA
    34. Shugart, YY; Cour, C; Renard, H; Lenoir, G; Goldgar, D; Teare, D; Easton, D; Rahman, N; Gusterton, R; Seal, S; Barfoot, R; Stratton, M; Mangion, J; Peelen, T; van den Ouweland, A; Meijers, H; Devilee, P; Eccles, D; Lynch, H; Weber, B; Stoppa-Lyonnet, D; Bignon, YJ
      Linkage analysis of 56 multiplex families excludes the Cowden disease genePTEN as a major contributor to familial breast cancer

      JOURNAL OF MEDICAL GENETICS
    35. Lauge, A; Lefebvre, C; Laurent-Puig, P; Caux, V; Gad, S; Eng, C; Longy, M; Stoppa-Lyonnet, D
      No evidence for germline PTEN mutations in families with breast and brain tumours

      INTERNATIONAL JOURNAL OF CANCER
    36. Sinilnikova, OM; Egan, KM; Quinn, JL; Boutrand, L; Lenoir, GM; Stoppa-Lyonnet, D; Desjardins, L; Levy, C; Goldgar, D; Gragcoudas, ES
      Germline brca2 sequence variants in patients with ocular melanoma

      INTERNATIONAL JOURNAL OF CANCER
    37. Puget, N; Stoppa-Lyonnet, D; Sinilnikova, OM; Pages, S; Lynch, HT; Lenoir, GM; Mazoyer, S
      Screening for germ-line rearrangements and regulatory mutations in BRCA1 led to the identification of four new deletions

      CANCER RESEARCH
    38. Eisinger, F; Alby, N; Bremond, A; Dauplat, J; Espie, M; Janiaud, P; Kuttenn, F; Lebrun, JP; Lefranc, JP; Pierret, J; Sobol, H; Stoppa-Lyonnet, D; Thouvenin, D; Tristant, H; Feingold, J
      Recommendations for medical management of hereditary breast and ovarian cancer: the Inserm-FNCLCC ad hoc committee

      BULLETIN DU CANCER
    39. Janin, N; Andrieu, N; Ossian, K; Lauge, A; Croquette, MF; Griscelli, C; Debre, M; Bressac-de-Paillerets, B; Aurias, A; Stoppa-Lyonnet, D
      Breast cancer risk in ataxia telangiectasia (AT) heterozygotes: haplotype study in French AT families

      BRITISH JOURNAL OF CANCER
    40. Eisinger, F; Alby, N; Bremond, A; Dauplat, J; Espie, M; Janiaud, P; Kuttenn, F; Lebrun, JP; Lefranc, JP; Pierret, J; Sobol, H; Stoppa-Lyonnet, D; Thouvenin, D; Tristant, H; Feingold, J
      Recommendations for medical management of hereditary breast and ovarian cancer: the INSERM-FNCLCC ad hoc committee

      ANNALES DE GENETIQUE
    41. Mefford, HC; Baumbach, L; Panguluri, RCK; Whitfield-Broome, C; Szabo, C; Smith, S; King, MC; Dunston, G; Stoppa-Lyonnet, D; Arena, F
      Evidence for a BRCA1 founder mutation in families of west African ancestry

      AMERICAN JOURNAL OF HUMAN GENETICS
    42. Puget, N; Sinilnikova, OM; Stoppa-Lyonnet, D; Audoynaud, C; Pages, S; Lynch, HT; Goldgar, D; Lenoir, GM; Mazoyer, S
      An Alu-mediated 6-kb duplication in the BRCA1 gene: A new founder mutation?

      AMERICAN JOURNAL OF HUMAN GENETICS
    43. Eisinger, F; Alby, N; Bremond, A; Dauplat, J; Espie, M; Janiaud, P; Kuttenn, F; Lebrun, JP; Lefranc, JP; Pierret, J; Sobol, H; Stoppa-Lyonnet, D; Thouvenin, D; Tristant, H; Feingold, J
      Recommendations for medical management of hereditary breast and ovarian cancer: The INSERM-FNCLCC ad hoc committee

      ANNALES D ENDOCRINOLOGIE
    44. Serova-Sinilnikova, O; Egan, K; Boutrand, L; Stoppa-Lyonnet, D; Desjardins, L; Levy, C; Bignon, YJ; Lasset, C; Haguenauer, O; Goldgar, D; Lenoir, GM
      Implication of germline BRCA2 gene mutations for the occurrence of ocular melanoma and pancreatic cancer

      EUROCANCER 98


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Documento generato il 09/08/20 alle ore 01:33:31