Hakutulokset - Stefan Aretz

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  1. 1
    The Differential Diagnosis and Early Detection of Hereditary Gastrointestinal Polyposis Syndromes

    The Differential Diagnosis and Early Detection of Hereditary Gastrointestinal Polyposis Syndromes Tekijä Stefan Aretz

    Julkaistu 2010
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  2. 2
    The differential diagnosis and surveillance of hereditary gastrointestinal polyposis syndromes.

    The differential diagnosis and surveillance of hereditary gastrointestinal polyposis syndromes. Tekijä Stefan Aretz

    Julkaistu 2010
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  3. 3
    Large submicroscopic genomic APC deletions are a common cause of typical familial adenomatous polyposis

    Large submicroscopic genomic APC deletions are a common cause of typical familial adenomatous polyposis Tekijä Stefan Aretz

    Julkaistu 2005
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  4. 4
    Familial Adenomatous Polyposis: Experience from a Study of 1164 Unrelated German Polyposis Patients

    Familial Adenomatous Polyposis: Experience from a Study of 1164 Unrelated German Polyposis Patients Tekijä Waltraut Friedl, Stefan Aretz

    Julkaistu 2005
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  5. 5
    Frequency and parental origin of de novo APC mutations in familial adenomatous polyposis

    Frequency and parental origin of de novo APC mutations in familial adenomatous polyposis Tekijä Stefan Aretz, Siegfried Uhlhaas, Reiner Caspari, Elisabeth Mangold, Constanze Pagenstecher, Peter Propping, Waltraut Friedl

    Julkaistu 2003
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  6. 6
    Somatic<i>APC</i>mosaicism: a frequent cause of familial adenomatous polyposis (FAP)

    Somatic<i>APC</i>mosaicism: a frequent cause of familial adenomatous polyposis (FAP) Tekijä Stefan Aretz, Dietlinde Stienen, Nicolaus Friedrichs, Susanne Stemmler, Siegfried Uhlhaas, Nils Rahner, Peter Propping, Waltraut Friedl

    Julkaistu 2007
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  7. 7
    <i>MUTYH</i>‐associated polyposis: 70 of 71 patients with biallelic mutations present with an attenuated or atypical phenotype

    <i>MUTYH</i>‐associated polyposis: 70 of 71 patients with biallelic mutations present with an attenuated or atypical phenotype Tekijä Stefan Aretz, Siegfried Uhlhaas, Heike Goergens, Kirsten Siberg, Matthias Vogel, Constanze Pagenstecher, Elisabeth Mangold, Reiner Caspari, Peter Propping, Waltraut Friedl

    Julkaistu 2006
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  8. 8
    Breast and prostate cancer risk: The interplay of polygenic risk, rare pathogenic germline variants, and family history

    Breast and prostate cancer risk: The interplay of polygenic risk, rare pathogenic germline variants, and family history Tekijä Emadeldin Hassanin, Patrick May, Rana Aldisi, Isabel Spier, Andreas J. Forstner, Markus M. Nöthen, Stefan Aretz, Peter Krawitz, Dheeraj Reddy Bobbili, Carlo Maj

    Julkaistu 2021
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  9. 9
    Deep intronic<i>APC</i>mutations explain a substantial proportion of patients with familial or early-onset adenomatous polyposis

    Deep intronic<i>APC</i>mutations explain a substantial proportion of patients with familial or early-onset adenomatous polyposis Tekijä Isabel Spier, Sukanya Horpaopan, Stefanie Vogt, Siegfried Uhlhaas, Monika Morak, Dietlinde Stienen, Markus Draaken, Michael Ludwig, Elke Holinski‐Feder, Markus M. Nöthen, Per Hoffmann, Stefan Aretz

    Julkaistu 2012
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  10. 10
    Real‐time use of artificial intelligence (CADEYE) in colorectal cancer surveillance of patients with Lynch syndrome—A randomized controlled pilot trial (CADLY)

    Real‐time use of artificial intelligence (CADEYE) in colorectal cancer surveillance of patients with Lynch syndrome—A randomized controlled pilot trial (CADLY) Tekijä Robert Hüneburg, Karolin Bucksch, Friederike Schmeißer, Dominik Heling, Tim Marwitz, Stefan Aretz, Dominik J. Kaczmarek, Glen Kristiansen, Oliver Hommerding, Christian P. Strassburg, Christoph Engel, Jacob Nattermann

    Julkaistu 2022
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  11. 11
    High proportion of large genomic STK11 deletions in Peutz-Jeghers syndrome

    High proportion of large genomic STK11 deletions in Peutz-Jeghers syndrome Tekijä Stefan Aretz, Dietlinde Stienen, Siegfried Uhlhaas, Steffan Loff, Walter Back, Constanze Pagenstecher, D. Ross McLeod, Gail E. Graham, Elisabeth Mangold, René Santer, Peter Propping, Waltraut Friedl

    Julkaistu 2005
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  12. 12
    Expanded Extracolonic Tumor Spectrum in MUTYH-Associated Polyposis

    Expanded Extracolonic Tumor Spectrum in MUTYH-Associated Polyposis Tekijä Stefanie Vogt, Natalie B. Jones, Daria Christian, Christoph Engel, Maartje Nielsen, Astrid Kaufmann, Verena Steinke, Hans F. A. Vasen, Peter Propping, Julian R. Sampson, Frederik J. Hes, Stefan Aretz

    Julkaistu 2009
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  13. 13
    Analysis of MUTYH Genotypes and Colorectal Phenotypes in Patients With MUTYH-Associated Polyposis

    Analysis of MUTYH Genotypes and Colorectal Phenotypes in Patients With MUTYH-Associated Polyposis Tekijä Maartje Nielsen, Mirjam C. Joerink - van de Beld, Natalie B. Jones, Stefanie Vogt, Carli M.J. Tops, Hans F. A. Vasen, Julian R. Sampson, Stefan Aretz, Frederik J. Hes

    Julkaistu 2008
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  14. 14
    Autoimmunity, Intestinal Lymphoid Hyperplasia, and Defects in Mucosal B-Cell Homeostasis in Patients With PTEN Hamartoma Tumor Syndrome

    Autoimmunity, Intestinal Lymphoid Hyperplasia, and Defects in Mucosal B-Cell Homeostasis in Patients With PTEN Hamartoma Tumor Syndrome Tekijä Mario Heindl, Norman Händel, Joanne Ngeow, Janina Kionke, Christian Wittekind, Manja Kamprad, Anne Rensing‐Ehl, Stephan Ehl, J. Reifenberger, Christoph Loddenkemper, Jochen Maul, Albrecht Hoffmeister, Stefan Aretz, Wieland Kieß, Charis Eng, Holm H. Uhlig

    Julkaistu 2012
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  15. 15
    MUTYH-associated polyposis (MAP): evidence for the origin of the common European mutations p.Tyr179Cys and p.Gly396Asp by founder events

    MUTYH-associated polyposis (MAP): evidence for the origin of the common European mutations p.Tyr179Cys and p.Gly396Asp by founder events Tekijä Stefan Aretz, Rossella Tricarico, Laura Papi, Isabel Spier, Elisa Pin, Sukanya Horpaopan, Emanuela Lucci‐Cordisco, Monica Pedroni, Dietlinde Stienen, Annamaria Gentile, Anna Panza, Ada Piepoli, Maurizio Ponz de Leòn, Waltraut Friedl, Alessandra Viel, Maurizio Genuardi

    Julkaistu 2013
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  16. 16
    High proportion of large genomic deletions and a genotype phenotype update in 80 unrelated families with juvenile polyposis syndrome

    High proportion of large genomic deletions and a genotype phenotype update in 80 unrelated families with juvenile polyposis syndrome Tekijä Stefan Aretz, Dietlinde Stienen, Siegfried Uhlhaas, M. Stolte, Mark M. Entius, Steffan Loff, Walter Back, Astrid Kaufmann, KM Keller, Stefan Blaas, Reiner Siebert, Stefanie Vogt, S Spranger, Elke Holinski‐Feder, Lone Sunde, Peter Propping, W Friedl

    Julkaistu 2007
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  17. 17
    The Management of Peutz–Jeghers Syndrome: European Hereditary Tumour Group (EHTG) Guideline

    The Management of Peutz–Jeghers Syndrome: European Hereditary Tumour Group (EHTG) Guideline Tekijä Anja Wagner, Stefan Aretz, Annika Auranen, Marco J. Bruno, Giulia Martina Cavestro, Emma J. Crosbie, Anne Goverde, Anne Marie Jelsig, Andrew Latchford, Monique E. van Leerdam, Anna Lepistö, Marta Puzzono, Ingrid Winship, Veronica Zuber, Gabriela Möslein

    Julkaistu 2021
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  18. 18
    Clinically relevant combined effect of polygenic background, rare pathogenic germline variants, and family history on colorectal cancer incidence

    Clinically relevant combined effect of polygenic background, rare pathogenic germline variants, and family history on colorectal cancer incidence Tekijä Emadeldin Hassanin, Isabel Spier, Dheeraj Reddy Bobbili, Rana Aldisi, Hannah Klinkhammer, Friederike S. David, Núria Dueñas, Robert Hüneburg, Claudia Perne, Joan Brunet, Gabriel Capellà, Markus M. Nöthen, Andreas J. Forstner, Andreas Mayr, Peter Krawitz, Patrick May, Stefan Aretz, Carlo Maj

    Julkaistu 2023
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  19. 19
    Frequency and phenotypic spectrum of germline mutations in<i>POLE</i>and seven other polymerase genes in 266 patients with colorectal adenomas and carcinomas

    Frequency and phenotypic spectrum of germline mutations in<i>POLE</i>and seven other polymerase genes in 266 patients with colorectal adenomas and carcinomas Tekijä Isabel Spier, Stefanie Holzapfel, Janine Altmüller, Bixiao Zhao, Sukanya Horpaopan, Stefanie Vogt, Sophia Chen, Monika Morak, Susanne Raeder, Katrin Kayser, Dietlinde Stienen, R. Adam, Peter Nürnberg, Guido Plotz, Elke Holinski‐Feder, Richard P. Lifton, Hölger Thiele, Per Hoffmann, Verena Steinke, Stefan Aretz

    Julkaistu 2014
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  20. 20
    Disease expression in juvenile polyposis syndrome: a retrospective survey on a cohort of 221 European patients and comparison with a literature-derived cohort of 473 SMAD4/BMPR1A pathogenic variant carriers

    Disease expression in juvenile polyposis syndrome: a retrospective survey on a cohort of 221 European patients and comparison with a literature-derived cohort of 473 SMAD4/BMPR1A p... Tekijä Robert Blatter, Benjamin Tschupp, Stefan Aretz, Inge Bernstein, Chrystelle Colas, D. Gareth Evans, Maurizio Genuardi, Frederik J. Hes, Robert Hüneburg, Heikki Järvinen, Fiona Lalloo, Gabriela Möslein, Laura Renkonen‐Sinisalo, Nicoletta Resta, Isabel Spier, Dora Varvara, Hans F. A. Vasen, Andrew Latchford, Karl Heinimann

    Julkaistu 2020
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