Resultats de la cerca - Judith Balmañà

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  1. 1
    BRCA in breast cancer: ESMO Clinical Practice Guidelines

    BRCA in breast cancer: ESMO Clinical Practice Guidelines per Judith Balmañà, Orland Dı́ez, Isabel T. Rubio, M. Castiglione

    Publicat 2010
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  2. 2
    Familial risk-colorectal cancer: ESMO Clinical Practice Guidelines

    Familial risk-colorectal cancer: ESMO Clinical Practice Guidelines per Judith Balmañà, Francesc Balaguer, Andrés Cervantes, Dirk Arnold

    Publicat 2013
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  3. 3
    Controversies in oncology: are genomic tests quantifying homologous recombination repair deficiency (HRD) useful for treatment decision making?

    Controversies in oncology: are genomic tests quantifying homologous recombination repair deficiency (HRD) useful for treatment decision making? per Benedetta Pellegrino, Joaquı́n Mateo, Violeta Serra, Judith Balmañà

    Publicat 2019
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  4. 4
    BRCA in breast cancer: ESMO Clinical Practice Guidelines

    BRCA in breast cancer: ESMO Clinical Practice Guidelines per Judith Balmañà, Orland Dı́ez, Isabel T. Rubio, Fátima Cardoso

    Publicat 2011
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  5. 5
    Hereditary gastrointestinal cancers: ESMO Clinical Practice Guidelines for diagnosis, treatment and follow-up†

    Hereditary gastrointestinal cancers: ESMO Clinical Practice Guidelines for diagnosis, treatment and follow-up† per Neda Stjepanovic, Leticia Moreira, Fátima Carneiro, Francesc Balaguer, Andrés Cervantes, Judith Balmañà, Erika Martinelli

    Publicat 2019
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  6. 6
    Microsatellite instability due to hMLH1 deficiency is associated with increased cytotoxicity to irinotecan in human colorectal cancer cell lines

    Microsatellite instability due to hMLH1 deficiency is associated with increased cytotoxicity to irinotecan in human colorectal cancer cell lines per Eduardo Vilar, Maurizio Scaltriti, Judith Balmañà, Cristina Saura, Marta Guzmán, Joaquı́n Arribas, José Baselga, Josep Tabernero

    Publicat 2008
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  7. 7
    Prevention and screening in BRCA mutation carriers and other breast/ovarian hereditary cancer syndromes: ESMO Clinical Practice Guidelines for cancer prevention and screening

    Prevention and screening in BRCA mutation carriers and other breast/ovarian hereditary cancer syndromes: ESMO Clinical Practice Guidelines for cancer prevention and screening per Shani Paluch‐Shimon, Fátima Cardoso, Cristiana Sessa, Judith Balmañà, Maria João Cardoso, Fiona J. Gilbert, Elżbieta Senkus

    Publicat 2016
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  8. 8
    Moving From Poly (ADP-Ribose) Polymerase Inhibition to Targeting DNA Repair and DNA Damage Response in Cancer Therapy

    Moving From Poly (ADP-Ribose) Polymerase Inhibition to Targeting DNA Repair and DNA Damage Response in Cancer Therapy per Charlie Gourley, Judith Balmañà, Jonathan A. Ledermann, Violeta Serra, Rebecca Dent, Sibylle Loibl, Éric Pujade-Lauraine, Simon J. Boulton

    Publicat 2019
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  9. 9
    Validation and Extension of the PREMM1,2 Model in a Population-Based Cohort of Colorectal Cancer Patients

    Validation and Extension of the PREMM1,2 Model in a Population-Based Cohort of Colorectal Cancer Patients per Francesc Balaguer, Judith Balmañà, Sergi Castellví–Bel, Ewout W. Steyerberg, Montserrat Andreu, Xavier Llor, Rodrigo Jover, Sapna Syngal, Antoni Castells

    Publicat 2007
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  10. 10
    Development and Validation of a Colon Cancer Risk Assessment Tool for Patients Undergoing Colonoscopy

    Development and Validation of a Colon Cancer Risk Assessment Tool for Patients Undergoing Colonoscopy per Fay Kastrinos, John I. Allen, David H. Stockwell, Elena M. Stoffel, E. Francis Cook, Muthoka L. Mutinga, Judith Balmañà, Sapna Syngal

    Publicat 2009
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  11. 11
    SEOM clinical guidelines in Hereditary Breast and ovarian cancer

    SEOM clinical guidelines in Hereditary Breast and ovarian cancer per Gemma Llort, Isabel Chirivella, Rafael Morales, Rafael Serrano del Rosal, A.B. Sánchez, Àlex Teulé, Elena Lastra, Joan Brunet, Judith Balmañà, Begoña Graña

    Publicat 2015
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  12. 12
    A decade of clinical development of PARP inhibitors in perspective

    A decade of clinical development of PARP inhibitors in perspective per Joaquı́n Mateo, Christopher J. Lord, Violeta Serra, Andrew Tutt, Judith Balmañà, Marta Castroviejo‐Bermejo, Cristina Cruz, Ana Oaknin, Stan B. Kaye, Johann S. de Bono

    Publicat 2019
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  13. 13
    Management of individuals with germline variants in PALB2: a clinical practice resource of the American College of Medical Genetics and Genomics (ACMG)

    Management of individuals with germline variants in PALB2: a clinical practice resource of the American College of Medical Genetics and Genomics (ACMG) per Marc Tischkowitz, Judith Balmañà, William D. Foulkes, Paul A. James, Joanne Ngeow, Rita K. Schmutzler, Nicoleta Voian, Myra J. Wick, Douglas R. Stewart, Tuya Pal

    Publicat 2021
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  14. 14
    Screening and surveillance in hereditary gastrointestinal cancers: Recommendations from the European Society of Digestive Oncology (ESDO) expert discussion at the 20th European Society for Medical Oncology (ESMO)/World Congress on Gastrointestinal Cancer, Barcelona, June 2018

    Screening and surveillance in hereditary gastrointestinal cancers: Recommendations from the European Society of Digestive Oncology (ESDO) expert discussion at the 20th European Soc... per Deepak Vangala, Estelle Cauchin, Judith Balmañà, Lucjan Wyrwicz, Eric Van Cutsem, Ulrich Güller, Antoni Castells, Fátima Carneiro, Pascal Hammel, Michel Ducreux, Jean‐Luc Van Laethem, Tamara Matysiak‐Budnik, Wolff Schmiegel

    Publicat 2018
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  15. 15
    Conflicting Interpretation of Genetic Variants and Cancer Risk by Commercial Laboratories as Assessed by the Prospective Registry of Multiplex Testing

    Conflicting Interpretation of Genetic Variants and Cancer Risk by Commercial Laboratories as Assessed by the Prospective Registry of Multiplex Testing per Judith Balmañà, Laura DiGiovanni, Pragna Gaddam, Michael F. Walsh, Joseph Vijai, Zsofia K. Stadler, Katherine L. Nathanson, Judy E. Garber, Fergus J. Couch, Kenneth Offit, Mark E. Robson, Susan M. Domchek

    Publicat 2016
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  16. 16
    Early Diagnosis of Oral Cancer and Lesions in Fanconi Anemia Patients: A Prospective and Longitudinal Study Using Saliva and Plasma

    Early Diagnosis of Oral Cancer and Lesions in Fanconi Anemia Patients: A Prospective and Longitudinal Study Using Saliva and Plasma per Ricardo Errazquin, Estela Carrasco, Sonia Del Marro, Anna Suñol, Jorge Peral, Jessica Ortiz, Juan Carlos Rubio, Carmen Segrelles, Marta Dueñas, Alicia Garrido-Aranda, Martina Álvarez, Cristina Beléndez, Judith Balmañà, Ramón García‐Escudero

    Publicat 2023
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  17. 17
    Population-based germline breast cancer gene association studies and meta-analysis to inform wider mainstream testing.

    Population-based germline breast cancer gene association studies and meta-analysis to inform wider mainstream testing. per Charlie F Rowlands, Sophie Allen, Judith Balmañà, Susan M. Domchek, D. Gareth Evans, Helen Hanson, Nicoline Hoogerbrugge, Philip James, K.L. Nathanson, Mark E. Robson, Marc Tischkowitz, William D. Foulkes, Clare Turnbull

    Publicat 2024
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  18. 18
    Comparison of the clinical prediction model PREMM<sub>1,2,6</sub>and molecular testing for the systematic identification of Lynch syndrome in colorectal cancer

    Comparison of the clinical prediction model PREMM<sub>1,2,6</sub>and molecular testing for the systematic identification of Lynch syndrome in colorectal cancer per Fay Kastrinos, Ewout W. Steyerberg, Judith Balmañà, Rowena Mercado, Steven Gallinger, Robert W. Haile, Graham Casey, John L. Hopper, Loı̈c Le Marchand, Noralane M. Lindor, Polly A. Newcomb, Stephen N. Thibodeau, Sapna Syngal

    Publicat 2012
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  19. 19
    BRCA1 intronic Alu elements drive gene rearrangements and PARP inhibitor resistance

    BRCA1 intronic Alu elements drive gene rearrangements and PARP inhibitor resistance per Yifan Wang, Andrea J. Bernhardy, Joseph Nacson, John J. Krais, Yinfei Tan, Émmanuelle Nicolas, Marc R. Radke, Elizabeth Handorf, Alba Llop‐Guevara, Judith Balmañà, Elizabeth M. Swisher, Violeta Serra, Suraj Peri, Neil Johnson

    Publicat 2019
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  20. 20
    Breast cancer phenotype in women with TP53 germline mutations: a Li-Fraumeni syndrome consortium effort

    Breast cancer phenotype in women with TP53 germline mutations: a Li-Fraumeni syndrome consortium effort per Serena Masciari, Deborah Dillon, M Rath, Mark E. Robson, Jeffrey N. Weitzel, Judith Balmañà, Stephen B. Gruber, James M. Ford, David Euhus, Alexandra Lebensohn, Melinda L. Telli, Stephen Pochebit, Georgios Lypas, Judy E. Garber

    Publicat 2012
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