Canlyniadau Chwilio - Margreet G.E.M. Ausems

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  1. 1
    A pre-visit website with question prompt sheet for counselees facilitates communication in the first consultation for breast cancer genetic counseling: findings from a randomized controlled trial

    A pre-visit website with question prompt sheet for counselees facilitates communication in the first consultation for breast cancer genetic counseling: findings from a randomized c... gan Akke Albada, Sandra van Dulmen, Margreet G.E.M. Ausems, Jozien M. Bensing

    Cyhoeddwyd 2012
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    Initial cancer genetic counseling consultation: Change in counselees' cognitions and anxiety, and association with addressing their needs and preferences

    Initial cancer genetic counseling consultation: Change in counselees' cognitions and anxiety, and association with addressing their needs and preferences gan Arwen H. Pieterse, Margreet G.E.M. Ausems, Sandra van Dulmen, Frits A. Beemer, Jozien M. Bensing

    Cyhoeddwyd 2005
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  3. 3
    Cancer Genetic Counseling: Communication and Counselees’ Post‐Visit Satisfaction, Cognitions, Anxiety, and Needs Fulfillment

    Cancer Genetic Counseling: Communication and Counselees’ Post‐Visit Satisfaction, Cognitions, Anxiety, and Needs Fulfillment gan Arwen H. Pieterse, Sandra van Dulmen, Frits A. Beemer, Jozien M. Bensing, Margreet G.E.M. Ausems

    Cyhoeddwyd 2007
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  4. 4
    Barriers to participating in genetic counseling and BRCA testing during primary treatment for breast cancer

    Barriers to participating in genetic counseling and BRCA testing during primary treatment for breast cancer gan Kathryn J. Schlich‐Bakker, H.F.J. ten Kroode, Carla C. Wárlám-Rodenhuis, Jan van den Bout, Margreet G.E.M. Ausems

    Cyhoeddwyd 2007
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  5. 5
    The Feasibility of Implementing Mainstream Germline Genetic Testing in Routine Cancer Care—A Systematic Review

    The Feasibility of Implementing Mainstream Germline Genetic Testing in Routine Cancer Care—A Systematic Review gan Kyra Bokkers, Michiel Vlaming, Ellen G. Engelhardt, Ronald P. Zweemer, Inge M. van Oort, Lambertus A. Kiemeney, Eveline M. A. Bleiker, Margreet G.E.M. Ausems

    Cyhoeddwyd 2022
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  6. 6
    Genotype‐phenotype correlation in adult‐onset acid maltase deficiency

    Genotype‐phenotype correlation in adult‐onset acid maltase deficiency gan John H. J. Wokke, Margreet G.E.M. Ausems, Marie‐José H. van den Boogaard, Elly F. Ippel, Otto van Diggelen, Marian A. Kroos, M. Boer, F.G.I. Jennekens, Arnold Reuser, Hans Kristian Ploos van Amstel

    Cyhoeddwyd 1995
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  7. 7
    Microsatellite Instability, Immunohistochemistry, and Additional PMS2 Staining in Suspected Hereditary Nonpolyposis Colorectal Cancer

    Microsatellite Instability, Immunohistochemistry, and Additional PMS2 Staining in Suspected Hereditary Nonpolyposis Colorectal Cancer gan Andrea E. van der Meulen–de Jong, Marjo van Puijenbroek, Yvonne Hendriks, Carli Tops, Juul Wijnen, Margreet G.E.M. Ausems, Hanne Meijers‐Heijboer, Anja Wagner, Theo A.M. van Os, Annette Bröcker‐Vriends, Hans F. A. Vasen, Hans Morreau

    Cyhoeddwyd 2004
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  8. 8
    Regular surveillance for Li-fraumeni syndrome: advice, adherence and perceived benefits

    Regular surveillance for Li-fraumeni syndrome: advice, adherence and perceived benefits gan Chantal R.M. Lammens, Eveline M. A. Bleiker, Neil K. Aaronson, Anja Wagner, Rolf H. Sijmons, Margreet G.E.M. Ausems, A. H. J. T. Vriends, Mariëlle Ruijs, Theo A.M. van Os, Liesbeth Spruijt, E. Gómez, Annemieke Cats, Tanja Nagtegaal, Senno Verhoef

    Cyhoeddwyd 2010
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  9. 9
    Genetic Testing in Li-Fraumeni Syndrome: Uptake and Psychosocial Consequences

    Genetic Testing in Li-Fraumeni Syndrome: Uptake and Psychosocial Consequences gan Chantal R.M. Lammens, Neil K. Aaronson, Anja Wagner, Rolf H. Sijmons, Margreet G.E.M. Ausems, A. H. J. T. Vriends, Mariëlle Ruijs, Theo A.M. van Os, Liesbeth Spruijt, E. Gómez, Irma Kluijt, Tanja Nagtegaal, Senno Verhoef, Eveline M. A. Bleiker

    Cyhoeddwyd 2010
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  10. 10
    Physical activity and the risk of breast cancer in BRCA1/2 mutation carriers

    Physical activity and the risk of breast cancer in BRCA1/2 mutation carriers gan Anouk Pijpe, Peggy Manders, Richard M. Brohet, J. Margriet Collée, Senno Verhoef, Hans F. A. Vasen, Nicoline Hoogerbrugge, Christi J. van Asperen, Charlotte J. Dommering, Margreet G.E.M. Ausems, Cora M. Aalfs, E. Gómez, Laura J. vanʼt Veer, Flora E. van Leeuwen, Matti A. Rookus

    Cyhoeddwyd 2009
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  11. 11
    <i>CDH1</i>‐related hereditary diffuse gastric cancer syndrome: Clinical variations and implications for counseling

    <i>CDH1</i>‐related hereditary diffuse gastric cancer syndrome: Clinical variations and implications for counseling gan Irma Kluijt, Ester Siemerink, Margreet G.E.M. Ausems, Theo A.M. van Os, Daphne de Jong, Joana Simões‐Correia, J. Han van Krieken, Marjolijn J. L. Ligtenberg, Joana Figueiredo, E. van Riel, Rolf H. Sijmons, John Theodorus Plukker, Richard van Hillegersberg, Evelien Dekker, Carla Oliveíra, Annemieke Cats, Nicoline Hoogerbrugge

    Cyhoeddwyd 2011
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  12. 12
    MEN1-Dependent Breast Cancer: Indication for Early Screening? Results From the Dutch MEN1 Study Group

    MEN1-Dependent Breast Cancer: Indication for Early Screening? Results From the Dutch MEN1 Study Group gan Rachel S. van Leeuwaarde, Koen M.A. Dreijerink, Margreet G.E.M. Ausems, Hanneke J.B.H. Beijers, Olaf M. Dekkers, Wouter W. de Herder, Anouk N. van der Horst‐Schrivers, Madeleine L. Drent, Peter H. Bisschop, Bas Havekes, Petra H.M. Peeters, Ruud M. Pijnappel, Menno R. Vriens, Gerlof D. Valk

    Cyhoeddwyd 2017
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  13. 13
    TP53 germline mutation testing in 180 families suspected of Li-Fraumeni syndrome: mutation detection rate and relative frequency of cancers in different familial phenotypes

    TP53 germline mutation testing in 180 families suspected of Li-Fraumeni syndrome: mutation detection rate and relative frequency of cancers in different familial phenotypes gan Mariëlle Ruijs, S. Verhoef, M.A. Rookus, Roelof Pruntel, Annemarie H. van der Hout, F.B.L. Hogervorst, Irma Kluijt, Rolf H. Sijmons, Cora M. Aalfs, Anja Wagner, Margreet G.E.M. Ausems, Nicoline Hoogerbrugge, C. J. van Asperen, E. Gómez, Hanne Meijers‐Heijboer, Leo P. ten Kate, Fred H. Menko, Laura van ‘t Veer

    Cyhoeddwyd 2010
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  14. 14
    Identification of CANT1 Mutations in Desbuquois Dysplasia

    Identification of CANT1 Mutations in Desbuquois Dysplasia gan Céline Huber, Bénédicte Oulès, Marta Bértoli, Mounia Chami, Mélanie Fradin, Yasemin Alanay, L.I. Al-Gazali, Margreet G.E.M. Ausems, Pierre Bitoun, Denise P. Cavalcanti, Alexander Krebs, Martine Le Merrer, Geert Mortier, Yousef Shafeghati, Andrea Superti‐Furga, Stephen P. Robertson, Carine Le Goff, Andrea Onetti Muda, Patrizia Paterlini-Bréchot, Arnold Münnich, Valérie Cormier‐Daire

    Cyhoeddwyd 2009
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  15. 15
    Point Mutations Throughout the GLI3 Gene Cause Greig Cephalopolysyndactyly Syndrome

    Point Mutations Throughout the GLI3 Gene Cause Greig Cephalopolysyndactyly Syndrome gan Martha Kalff-Suske, Anja Wild, Juliane Topp, Martina Wessling, Eva‐Maria Jacobsen, Dorothea Bornholdt, Hartmut Engel, Holger Heuer, Cora M. Aalfs, Margreet G.E.M. Ausems, Rita Barone, A Herzog, Peter Heutink, Tessa Homfray, Gabriele Gillessen‐Kaesbach, R. König, J. Kunze, Peter Meinecke, Dietmar Müller, Renata Rizzo, Sibylle Strenge, Andrea Superti‐Furga, Karl‐Heinz Grzeschik

    Cyhoeddwyd 1999
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  16. 16
    Clinical applicability of the Polygenic Risk Score for breast cancer risk prediction in familial cases

    Clinical applicability of the Polygenic Risk Score for breast cancer risk prediction in familial cases gan Inge M. M. Lakeman, Mar D M Rodríguez-Girondo, Andrew Lee, Nandi Celosse, Merel E. Braspenning, Klaartje van Engelen, Irma van de Beek, Annemiek H van der Hout, E. Gómez, Arjen R. Mensenkamp, Margreet G.E.M. Ausems, Maartje J. Hooning, Muriel A. Adank, Antoinette Hollestelle, Marjanka K. Schmidt, Christi J. van Asperen, Peter Devilee

    Cyhoeddwyd 2022
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    BRCA1 mutation carriers have a lower number of mature oocytes after ovarian stimulation for IVF/PGD

    BRCA1 mutation carriers have a lower number of mature oocytes after ovarian stimulation for IVF/PGD gan I. A. P. Derks-Smeets, Theodora C van Tilborg, Aafke P.A. van Montfoort, Luc Smits, Helen L. Torrance, M. Meijer‐Hoogeveen, Frank J. Broekmans, Jos Dreesen, Aimée Paulussen, Vivianne C. G. Tjan‐Heijnen, Irene Homminga, Merel M.J. van den Berg, Margreet G.E.M. Ausems, Martine De Rycke, Christine de Die‐Smulders, Willem Verpoest, R. van Golde

    Cyhoeddwyd 2017
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    Survival after bilateral risk-reducing mastectomy in healthy BRCA1 and BRCA2 mutation carriers

    Survival after bilateral risk-reducing mastectomy in healthy BRCA1 and BRCA2 mutation carriers gan Bernadette A. M. Heemskerk‐Gerritsen, Agnes Jager, Linetta B. Koppert, A.I.M. Obdeijn, Margriet Collée, Hanne Meijers‐Heijboer, Denise J. Jenner, Hester S. A. Oldenburg, Klaartje van Engelen, Jakob de Vries, Christi J. van Asperen, Peter Devilee, Marinus J. Blok, C. Marleen Kets, Margreet G.E.M. Ausems, Caroline Seynaeve, Matti A. Rookus, Maartje J. Hooning

    Cyhoeddwyd 2019
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    Exposure to diagnostic radiation and risk of breast cancer among carriers of BRCA1/2 mutations: retrospective cohort study (GENE-RAD-RISK)

    Exposure to diagnostic radiation and risk of breast cancer among carriers of BRCA1/2 mutations: retrospective cohort study (GENE-RAD-RISK) gan Anouk Pijpe, Nadine Andrieu, D. F. Easton, Ausrele Kesminiene, Elisabeth Cardis, Catherine Noguès, Marion Gauthier‐Villars, C. Lasset, Jean Pierre Fricker, S. Peock, D Frost, D. Gareth Evans, Rosalind A. Eeles, J. Paterson, Peggy Manders, C. J. van Asperen, Margreet G.E.M. Ausems, Hanne Meijers-Heijboer, Isabelle Thierry-Chef, Michael Hauptmann, David E. Goldgar, Matti A. Rookus, F. E. van Leeuwen

    Cyhoeddwyd 2012
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    Quantification of sequence exchange events between<i>PMS2</i>and<i>PMS2CL</i>provides a basis for improved mutation scanning of Lynch syndrome patients

    Quantification of sequence exchange events between<i>PMS2</i>and<i>PMS2CL</i>provides a basis for improved mutation scanning of Lynch syndrome patients gan Heleen M. van der Klift, Carli M.J. Tops, Elsa C. Bik, Merel W. Boogaard, Anne-Marijke Borgstein, Kerstin Hansson, Margreet G.E.M. Ausems, E. Gómez, Andrew Green, Frederik J. Hes, Louise Izatt, Liselotte P. van Hest, Ángel Alonso, A. H. J. T. Vriends, Anja Wagner, Wendy A.G. van Zelst–Stams, Hans F. A. Vasen, Hans Morreau, Peter Devilee, Juul Wijnen

    Cyhoeddwyd 2010
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