Výsledky vyhledávání - Melyssa Aronson

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  1. 1
    Impaired monocyte function in liver cirrhosis.

    Impaired monocyte function in liver cirrhosis. Autor Avi Hassner, Y. Kletter, D Shlag, M Yedvab, Melyssa Aronson, Shlomo Shibolet

    Vydáno 1981
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  2. 2
    Oncologic surveillance for subjects with biallelic mismatch repair gene mutations: 10 year follow‐up of a kindred

    Oncologic surveillance for subjects with biallelic mismatch repair gene mutations: 10 year follow‐up of a kindred Autor Carol Durno, Melyssa Aronson, Uri Tabori, David Malkin, Steven Gallinger, Helen S. L. Chan

    Vydáno 2011
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  3. 3
    Tumor Microsatellite Instability and Clinical Outcome in Young Patients with Colorectal Cancer

    Tumor Microsatellite Instability and Clinical Outcome in Young Patients with Colorectal Cancer Autor Robert Gryfe, Hyeja Kim, Eugene Hsieh, Melyssa Aronson, Eric J. Holowaty, Shelley B. Bull, Mark Redston, Steven Gallinger

    Vydáno 2000
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  4. 4
    Colorectal cancer survivors undergoing genetic testing for hereditary non‐polyposis colorectal cancer: motivational factors and psychosocial functioning

    Colorectal cancer survivors undergoing genetic testing for hereditary non‐polyposis colorectal cancer: motivational factors and psychosocial functioning Autor M. J. Esplen, Lisa Madlensky, Melyssa Aronson, Heidi Rothenmund, Steve Gallinger, Kate Butler, Brenda B. Toner, Jiahui Wong, M. Manno, John McLaughlin

    Vydáno 2007
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  5. 5
    Penetrance of colorectal cancer among MLH1/MSH2 carriers participating in the colorectal cancer familial registry in Ontario

    Penetrance of colorectal cancer among MLH1/MSH2 carriers participating in the colorectal cancer familial registry in Ontario Autor Yun‐Hee Choi, Michelle Cotterchio, Gail McKeown‐Eyssen, Neerav Monga, Bharati Bapat, Kevin Boyd, Steven Gallinger, John McLaughlin, Melyssa Aronson, Laurent Briollais

    Vydáno 2009
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  6. 6
    High frequency of mismatch repair deficiency among pediatric high grade gliomas in <scp>J</scp>ordan

    High frequency of mismatch repair deficiency among pediatric high grade gliomas in <scp>J</scp>ordan Autor Nisreen Amayiri, Uri Tabori, Brittany Campbell, Doua Bakry, Melyssa Aronson, Carol Durno, Patricia Rakopoulos, David Malkin, Ibrahim Qaddoumi, Awni Musharbash, Maisa Swaidan, Éric Bouffet, Cynthia Hawkins, Maysa Al‐Hussaini

    Vydáno 2015
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  7. 7
    Comparison of clinical schemas and morphologic features in predicting Lynch syndrome in mutation‐positive patients with endometrial cancer encountered in the context of familial gastrointestinal cancer registries

    Comparison of clinical schemas and morphologic features in predicting Lynch syndrome in mutation‐positive patients with endometrial cancer encountered in the context of familial ga... Autor Paul M. Ryan, Anna Marie Mulligan, Melyssa Aronson, Sarah E. Ferguson, Bharati Bapat, Kara Semotiuk, Spring Holter, Janice S. Kwon, Steve E. Kalloger, C. Blake Gilks, Steven Gallinger, Aaron Pollett, Blaise Clarke

    Vydáno 2011
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  8. 8
    Diagnostic criteria for constitutional mismatch repair deficiency (CMMRD): recommendations from the international consensus working group

    Diagnostic criteria for constitutional mismatch repair deficiency (CMMRD): recommendations from the international consensus working group Autor Melyssa Aronson, Chrystelle Colas, Andrew Y. Shuen, Heather Hampel, William D. Foulkes, Hagit Baris Feldman, Yael Goldberg, Martine Muleris, Kami Wolfe Schneider, Rose B. McGee, Kory Jasperson, Arun Rangaswami, Laurence Brugières, Uri Tabori

    Vydáno 2021
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  9. 9
    Gastrointestinal cancers and neurofibromatosis type 1 features in children with a germline homozygous MLH1 mutation

    Gastrointestinal cancers and neurofibromatosis type 1 features in children with a germline homozygous MLH1 mutation Autor Steven Gallinger, Melyssa Aronson, Katayoon Shayan, Elyanne M. Ratcliffe, Justin T. Gerstle, Patricia C. Parkin, Heidi Rothenmund, Marina E. Croitoru, Ewa Baumann, Peter R. Durie, Rosanna Weksberg, Aaron Pollett, Robert H. Riddell, Bo Ngan, Ernest Cutz, Alain E. Lagarde, Helen S. L. Chan

    Vydáno 2004
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  10. 10
    High prevalence of mismatch repair deficiency in prostate cancers diagnosed in mismatch repair gene mutation carriers from the colon cancer family registry

    High prevalence of mismatch repair deficiency in prostate cancers diagnosed in mismatch repair gene mutation carriers from the colon cancer family registry Autor Christophe Rosty, Michael D. Walsh, Noralane M. Lindor, Stephen N. Thibodeau, Erin Mundt, Steven Gallinger, Melyssa Aronson, Aaron Pollett, John A. Baron, Sally‐Ann Pearson, Mark Clendenning, Rhiannon Walters, Belinda Nagler, William Crawford, Joanne Young, Ingrid Winship, Aung Ko Win, John L. Hopper, Mark A. Jenkins, Daniel D. Buchanan

    Vydáno 2014
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  11. 11
    Phenotype and Polyp Landscape in Serrated Polyposis Syndrome

    Phenotype and Polyp Landscape in Serrated Polyposis Syndrome Autor Christophe Rosty, Daniel D. Buchanan, Michael D. Walsh, Sally‐Ann Pearson, Erika Pavluk, Rhiannon Walters, Mark Clendenning, Kevin Spring, Mark A. Jenkins, Aung Ko Win, John L. Hopper, Kevin Sweet, Wendy L. Frankel, Melyssa Aronson, Steve Gallinger, Jack Goldblatt, Sonja Woodall, Julie Arnold, Neal I. Walker, Jeremy R. Jass, Susan Parry, Joanne Young

    Vydáno 2012
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  12. 12
    Mutations in the RAS/MAPK Pathway Drive Replication Repair–Deficient Hypermutated Tumors and Confer Sensitivity to MEK Inhibition

    Mutations in the RAS/MAPK Pathway Drive Replication Repair–Deficient Hypermutated Tumors and Confer Sensitivity to MEK Inhibition Autor Brittany Campbell, Melissa A. Galati, Simone C. Stone, Alexandra N. Riemenschneider, Melissa Edwards, Sumedha Sudhaman, Robert Siddaway, Martin Komosa, Nuno M. Nunes, Liana Nobre, A. Sorana Morrissy, Matthew Zatzman, Michal Zápotocký, Lazar Joksimovic, Sangeetha Kalimuthu, David Samuel, Gary Mason, Éric Bouffet, Daniel A. Morgenstern, Melyssa Aronson, Carol Durno, David Malkin, John M. Maris, Michael D. Taylor, Adam Shlien, Trevor J. Pugh, Pamela S. Ohashi, Cynthia Hawkins, Uri Tabori

    Vydáno 2021
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  13. 13
    Lower Cancer Incidence in Amsterdam-I Criteria Families Without Mismatch Repair Deficiency

    Lower Cancer Incidence in Amsterdam-I Criteria Families Without Mismatch Repair Deficiency Autor Noralane M. Lindor, Kari G. Rabe, Gloria M. Petersen, Robert W. Haile, Graham Casey, John A. Baron, Steve Gallinger, Bharati Bapat, Melyssa Aronson, John L. Hopper, Jeremy R. Jass, Loı̈c Le Marchand, John Grove, John D. Potter, Polly A. Newcomb, Jonathan P. Terdiman, Peggy Conrad, G. Möslein, Richard M. Goldberg, Argyrios Ziogas, Hoda Anton‐Culver, Mariza de Andrade, Kim Siegmund, Stephen N. Thibodeau, Lisa A. Boardman, Daniela Seminara

    Vydáno 2005
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  14. 14
    Effectiveness of the Genomics ADvISER decision aid for the selection of secondary findings from genomic sequencing: a randomized clinical trial

    Effectiveness of the Genomics ADvISER decision aid for the selection of secondary findings from genomic sequencing: a randomized clinical trial Autor Yvonne Bombard, Marc Clausen, Salma Shickh, Chloe Mighton, Selina Casalino, Raymond H. Kim, Sarah M. Muir, Lindsay Carlsson, Nancy N. Baxter, Adena Scheer, Christine Elser, Andrea Eisen, Seema Panchal, Tracy Graham, Melyssa Aronson, Carolyn Piccinin, Talia Mancuso, Kara Semotiuk, Michael F. Evans, June C. Carroll, Kenneth Offit, Mark E. Robson, Jada G. Hamilton, Emily Glogowski, Kasmintan A. Schrader, Raymond H. Kim, Jordan Lerner‐Ellis, Kevin E. Thorpe, Andreas Laupacis, Yvonne Bombard, Susan Randall Armel, Melyssa Aronson, Nancy N. Baxter, Ahmed M. Bayoumi, Kenneth Bond, June C. Carroll, Timothy Caulfield, Marc Clausen, Tammy Clifford, Iris Cohn, Irfan A. Dhalla, Craig C. Earle, Andrea Eisen, Christine Elser, M. Blair Evans, Tracy Graham, Emily Glogowski, Jada G. Hamilton, Wanrudee Isaranuwatchai, Monika Kastner, Raymond H. Kim, Andreas Laupacis, Jordan Lerner‐Ellis, Michelle Mujoomdar, Kenneth Offit, Seema Panchal, Mark E. Robson, Adena Scheer, Stephen W. Scherer, Kasmintan A. Schrader, Terrence Sullivan, Kevin E. Thorpe

    Vydáno 2019
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  15. 15
    Cancer Risks for Relatives of Patients With Serrated Polyposis

    Cancer Risks for Relatives of Patients With Serrated Polyposis Autor Aung Ko Win, Rhiannon Walters, Daniel D. Buchanan, Mark A. Jenkins, Kevin Sweet, Wendy L. Frankel, Albert de la Chapelle, Diane McKeone, Michael D. Walsh, Mark Clendenning, Sally‐Ann Pearson, Erika Pavluk, Belinda Nagler, John L. Hopper, Michael Gattas, Jack Goldblatt, Jill George, Graeme Suthers, Kerry Phillips, Sonja Woodall, Julie Arnold, Kathy Tucker, Michael Field, Sian Greening, Steve Gallinger, Melyssa Aronson, Renée Perrier, Michael O. Woods, Jane S. Green, Neal I. Walker, Christophe Rosty, Susan Parry, Joanne Young

    Vydáno 2012
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  16. 16
    PMS2 monoallelic mutation carriers: the known unknown

    PMS2 monoallelic mutation carriers: the known unknown Autor McKinsey L. Goodenberger, Brittany C. Thomas, Douglas L. Riegert‐Johnson, C. Richard Boland, Sharon E. Plon, Mark Clendenning, Aung Ko Win, Leigha Senter, Steven M. Lipkin, Zsofia K. Stadler, Finlay Macrae, Henry T. Lynch, Jeffrey N. Weitzel, Albert de la Chapelle, Sapna Syngal, Patrick M. Lynch, Susan Parry, Mark A. Jenkins, Steven Gallinger, Spring Holter, Melyssa Aronson, Polly A. Newcomb, Terrilea Burnett, Loı̈c Le Marchand, Pavel N. Pichurin, Heather Hampel, Jonathan P. Terdiman, Karen H. Lu, Stephen N. Thibodeau, Noralane M. Lindor

    Vydáno 2015
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  17. 17
    Germ Line Mutations of Mismatch Repair Genes in Hereditary Nonpolyposis Colorectal Cancer Patients with Small Bowel Cancer: International Society for Gastrointestinal Hereditary Tumours Collaborative Study

    Germ Line Mutations of Mismatch Repair Genes in Hereditary Nonpolyposis Colorectal Cancer Patients with Small Bowel Cancer: International Society for Gastrointestinal Hereditary Tu... Autor Jae‐Gahb Park, Duck-Woo Kim, Chang Won Hong, Byung‐Ho Nam, Young‐Kyoung Shin, Sung-Hye Hong, Il-Jin Kim, Seok‐Byung Lim, Melyssa Aronson, Marie Luise Bisgaard, Gregor J. Brown, John Burn, Elizabeth Chow, Peggy Conrad, Fiona Douglas, Malcolm G. Dunlop, James M. Ford, Marc S. Greenblatt, Heikki Järvinen, Karl Heinimann, Elly Lynch, Finlay Macrae, Wendy McKinnon, Gabriela Möslein, Bernard Rossi, Paul Rozen, Lyn Schofield, Carlos Vaccaro, Hans F. A. Vasen, Mary E. Velthuizen, Alessandra Viel, Juul Wijnen

    Vydáno 2006
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  18. 18
    Finding the sweet spot: a qualitative study exploring patients’ acceptability of chatbots in genetic service delivery

    Finding the sweet spot: a qualitative study exploring patients’ acceptability of chatbots in genetic service delivery Autor Stephanie Luca, Marc Clausen, Angela Shaw, Whiwon Lee, Suvetha Krishnapillai, Ella Adi-Wauran, Hanna Faghfoury, Gregory Costain, Rebekah Jobling, Melyssa Aronson, Eriskay Liston, Josh Silver, Cheryl Shuman, Lauren Chad, Robin Z. Hayeems, Yvonne Bombard, François Bernier, Michael Brudno, June C. Carroll, Ronald D. Cohn, Irfan A. Dhalla, Jan M. Friedman, Stacy Hewson, Trevor Jamieson, Rita Kodida, Anne‐Marie Laberge, Jordan Lerner‐Ellis, Muhammad Mamdani, Christian R. Marshall, Matthew Osmond, Quỳnh Phạm, Emma Reble, Frank Rudzicz, Emily Seto, Serena Shastri-Estrada, Maureen Smith, Kevin E. Thorpe, Wendy J. Ungar

    Vydáno 2023
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  19. 19
    Risks of Lynch Syndrome Cancers for MSH6 Mutation Carriers

    Risks of Lynch Syndrome Cancers for MSH6 Mutation Carriers Autor Laura Baglietto, Noralane M. Lindor, James G. Dowty, Darren M. White, Anja Wagner, E. Gómez, A. H. J. T. Vriends, Nicola Cartwright, Rebecca A. Barnetson, Susan M. Farrington, Albert Tenesa, Heather Hampel, Daniel D. Buchanan, Sven Arnold, Joanne Young, Michael D. Walsh, Jeremy R. Jass, Finlay Macrae, Yoland Antill, Ingrid Winship, Graham G. Giles, Jack Goldblatt, Susan Parry, Graeme Suthers, Barbara Leggett, Malinda L. Butz, Melyssa Aronson, Jenny N. Poynter, John A. Baron, Loı̈c Le Marchand, Robert W. Haile, Steve Gallinger, John L. Hopper, John D. Potter, Albert de la Chapelle, Hans F. A. Vasen, Malcolm G. Dunlop, Stephen N. Thibodeau, Mark A. Jenkins

    Vydáno 2009
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  20. 20
    Genomic Microsatellite Signatures Identify Germline Mismatch Repair Deficiency and Risk of Cancer Onset

    Genomic Microsatellite Signatures Identify Germline Mismatch Repair Deficiency and Risk of Cancer Onset Autor Jiil Chung, Logine Negm, Vanessa Bianchi, Lucie Stengs, Anirban Das, Zhihui Amy Liu, Sumedha Sudhaman, Melyssa Aronson, Ledia Brunga, Melissa Edwards, Victoria J. Forster, Martin Komosa, Scott Davidson, Jodi Lees, Patrick Tomboc, David Samuel, Roula Farah, Anne Bendel, Jeffrey Knipstein, Kami Wolfe Schneider, Agnes Reschke, Shayna Zelcer, Alexandra P. Zorzi, Robert R. McWilliams, William D. Foulkes, Raymond Bedgood, Lindsay L. Peterson, Sara Rhode, An Van Damme, Isabelle Scheers, Sharon L. Gardner, Gabriel Robbins, Magimairajan Vanan, M. Stephen Meyn, Rebecca C. Auer, Brandie Heald, Carol A. Burke, Anita Villani, David Malkin, Éric Bouffet, Annie Huang, Michael D. Taylor, Carol Durno, Adam Shlien, Cynthia Hawkins, Gad Getz, Yosef E. Maruvka, Uri Tabori

    Vydáno 2022
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