検索結果 - Karin Mayer
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Genome-wide single-nucleotide polymorphism analysis in juvenile myelomonocytic leukemia identifies uniparental disomy surrounding the NF1 locus in cases associated with neurofibrom... 著者: Christian Flotho, Doris Steinemann, Charles G. Mullighan, Geoffrey Neale, Karin Mayer, Christian P. Kratz, Brigitte Schlegelberger, James R. Downing, Charlotte M. Niemeyer
出版事項 2007Artigo -
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The Role of Adding Somatostatin Analogues to Peptide Receptor Radionuclide Therapy as a Combination and Maintenance Therapy 著者: Anna Yordanova, Marcel M. Wicharz, Karin Mayer, Peter Brossart, Maria A. González-Carmona, Christian P. Strassburg, Rolf Fimmers, Markus Essler, Hojjat Ahmadzadehfar
出版事項 2018Artigo -
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Influenza virus infections in patients with malignancies –– characteristics and outcome of the season 2014/15. A survey conducted by the Infectious Diseases Working Party (AGIHO) o... 著者: Beate Hermann, Nicola Lehners, Michael Brodhun, Katharina Boden, Andreas Hochhaus, Matthias Kochanek, Katharina Meckel, Karin Mayer, Tobias Rachow, C. Rieger, Enrico Schalk, Thomas Weber, A. Schmeier-Jürchott, Peter Schlattmann, Daniel Teschner, Marie von Lilienfeld‐Toal
出版事項 2016Artigo -
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Primary prophylaxis of bacterial infections and Pneumocystis jirovecii pneumonia in patients with hematologic malignancies and solid tumors: 2020 updated guidelines of the Infectio... 著者: Annika Y. Claßen, Larissa Henze, Marie von Lilienfeld‐Toal, Georg Maschmeyer, Michael Sandherr, Luisa Durán Graeff, Nael Alakel, Maximilian Christopeit, Stefan W. Krause, Karin Mayer, Silke Neumann, Oliver A. Cornely, Olaf Penack, Florian Weißinger, Hans‐Heinrich Wolf, Jörg Janne Vehreschild
出版事項 2021Artigo -
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Functional Assessment of<i>TSC2</i>Variants Identified in Individuals with Tuberous Sclerosis Complex 著者: Marianne Hoogeveen‐Westerveld, Rosemary Ekong, Sue Povey, Karin Mayer, N. Lannoy, Frances Elmslie, Martina Bebin, Kira A. Dies, Catherine Thompson, Steven Sparagana, Peter Maxwell Davies, Agnies M. van Eeghen, Elizabeth A. Thiele, Ans van den Ouweland, Dicky Halley, Mark Nellist
出版事項 2013Artigo -
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Prognosis Factors in Probands With an FBN1 Mutation Diagnosed Before the Age of 1 Year 著者: Chantal Stheneur, Laurence Faivre, Gwenaëlle Collod‐Béroud, Élodie Gautier, Christine Binquet, Claire Bonithon‐Kopp, Mireille Claustres, Anne H. Child, Eloisa Arbustini, Lesley C. Adès, Uta Francke, Karin Mayer, Mine Arslan‐Kirchner, Anne De Paepe, Bertrand Chevallier, Damien Bonnet, Guillaume Jondeau, Cathérine Boileau
出版事項 2010Artigo -
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Community acquired respiratory virus infections in cancer patients—Guideline on diagnosis and management by the Infectious Diseases Working Party of the German Society for haematol... 著者: Marie von Lilienfeld‐Toal, Annemarie Berger, Maximilian Christopeit, Marcus Hentrich, Claus Peter Heußel, Jana Kalkreuth, Michael Klein, Matthias Kochanek, Olaf Penack, Elke Hauf, Christina Rieger, Gerda Silling, Maria J. G. T. Vehreschild, Thomas Weber, Hans‐Heinrich Wolf, Nicola Lehners, Enrico Schalk, Karin Mayer
出版事項 2016Revisão -
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Anti-infective vaccination strategies in patients with hematologic malignancies or solid tumors—Guideline of the Infectious Diseases Working Party (AGIHO) of the German Society for... 著者: C. Rieger, Blasius Liss, Sibylle C. Mellinghoff, Dieter Buchheidt, Oliver A. Cornely, Gerlinde Egerer, Werner Heinz, Marcus Hentrich, Georg Maschmeyer, Karin Mayer, Michael Sandherr, Gerda Silling, Andrew J. Ullmann, Maria J. G. T. Vehreschild, Marie von Lilienfeld‐Toal, H.-H. Wolf, Nicola Lehners
出版事項 2018Revisão -
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Long-Term Efficacy and Safety of Luspatercept for Anemia Treatment in Patients With Lower-Risk Myelodysplastic Syndromes: The Phase II PACE-MDS Study 著者: Uwe Platzbecker, Katharina S. Götze, Philipp Kiewe, Ulrich Germing, Karin Mayer, Markus P. Radsak, Thomas Wolff, Jöerg Chromik, Katja Sockel, Uta Oelschlägel, Detlef Haase, Thomas Illmer, Haifa Kathrin Al‐Ali, Gerda Silling, Joseph G. Reynolds, Xiaosha Zhang, Kenneth M. Attie, Jeevan K. Shetty, Aristoteles Giagounidis
出版事項 2022Artigo -
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Impact of myelodysplasia‐related and additional gene mutations in intensively treated patients with <i>NPM1</i>‐mutated AML 著者: Sibylle Cocciardi, Maral Saadati, Nina Weiß, Daniela Späth, Silke Kapp‐Schwoerer, Isabelle Schneider, Annika Meid, Verena I. Gaidzik, Sabrina Skambraks, Walter Fiedler, Michael W.M. Kühn, Ulrich Germing, Karin Mayer, Michael Lübbert, Elli Papaemmanuil, Felicitas Thol, Michael Heuser, Arnold Ganser, Lars Bullinger, Axel Benner, Hartmut Döhner, Konstanze Döhner
出版事項 2025Artigo -
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Primary prophylaxis of invasive fungal infections in patients with haematological malignancies: 2017 update of the recommendations of the Infectious Diseases Working Party (AGIHO)... 著者: Sibylle C. Mellinghoff, Jens Panse, Nael Alakel, Gerhard Behre, Dieter Buchheidt, Maximilian Christopeit, Justin Hasenkamp, Michael Kiehl, Michael Koldehoff, Stefan W. Krause, Nicola Lehners, Marie von Lilienfeld‐Toal, Annika Löhnert, Georg Maschmeyer, Daniel Teschner, Andrew J. Ullmann, Olaf Penack, Markus Ruhnke, Karin Mayer, Helmut Ostermann, H.-H. Wolf, Oliver A. Cornely
出版事項 2017Revisão -
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Cardiovascular manifestations in men and women carrying a FBN1 mutation 著者: Delphine Détaint, Laurence Faivre, Gwenaëlle Collod‐Béroud, Anne H. Child, Bart Loeys, Christine Binquet, Élodie Gautier, Eloisa Arbustini, Karin Mayer, Mine Arslan‐Kirchner, Chantal Stheneur, Dorothy Halliday, Christophe Béroud, Claire Bonithon‐Kopp, Mireille Claustres, Henri Plauchu, Peter N. Robinson, Anatoli Kiotsekoglou, Julie De Backer, Lesley C. Adès, Uta Francke, Anne De Paepe, Cathérine Boileau, Guillaume Jondeau
出版事項 2010Artigo -
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Contribution of molecular analyses in diagnosing Marfan syndrome and type I fibrillinopathies: an international study of 1009 probands 著者: Laurence Faivre, Gwenaëlle Collod‐Béroud, Anne H. Child, Bert Callewaert, Bart Loeys, Christine Binquet, Élodie Gautier, Eloisa Arbustini, Karin Mayer, Mine Arslan‐Kirchner, Chantal Stheneur, Anatoli Kiotsekoglou, Paolo Comeglio, Nicola Marziliano, Dorothy Halliday, Christophe Béroud, Claire Bonithon‐Kopp, Mireille Claustres, H Plauchu, Peter N. Robinson, Lesley C. Adès, Julie De Backer, Paul Coucke, Uta Francke, Anne De Paepe, Cathérine Boileau, Guillaume Jondeau
出版事項 2008Artigo -
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Clinical and mutation-type analysis from an international series of 198 probands with a pathogenic FBN1 exons 24–32 mutation 著者: Laurence Faivre, Gwenaëlle Collod‐Béroud, Bert Callewaert, A. H. Child, Christine Binquet, Élodie Gautier, Bart Loeys, Eloisa Arbustini, Karin Mayer, Mine Arslan‐Kirchner, C. Stheneur, Anatoli Kiotsekoglou, Paolo Comeglio, Nicola Marziliano, J. E. Wolf, O. Bouchot, Philippe Khau Van Kien, Christophe Béroud, Mireille Claustres, C. Bonithon-Kopp, Peter N. Robinson, Lesley C. Adès, Julie De Backer, Paul Coucke, Uta Francke, Anne De Paepe, Guillaume Jondeau, Cathérine Boileau
出版事項 2008Artigo -
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Clinical and Molecular Study of 320 Children With Marfan Syndrome and Related Type I Fibrillinopathies in a Series of 1009 Probands With Pathogenic <i>FBN1</i> Mutations 著者: Laurence Faivre, Alice Masurel‐Paulet, Gwenaëlle Collod‐Béroud, Bert Callewaert, Anne H. Child, Chantal Stheneur, Christine Binquet, Élodie Gautier, Bertrand Chevallier, Frédéric Huet, Bart Loeys, Eloisa Arbustini, Karin Mayer, Mine Arslan‐Kirchner, Anatoli Kiotsekoglou, Paolo Comeglio, Maurizia Grasso, Dorothy Halliday, Christophe Béroud, Claire Bonithon‐Kopp, Mireille Claustres, Peter N. Robinson, Lesley C. Adès, Julie De Backer, Paul Coucke, Uta Francke, Anne De Paepe, Cathérine Boileau, Guillaume Jondeau
出版事項 2008Artigo -
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The new Ghent criteria for Marfan syndrome: what do they change? 著者: Laurence Faivre, Gwenaëlle Collod‐Béroud, Lesley C. Adès, Eloisa Arbustini, Anne H. Child, Bert Callewaert, Bart Loeys, Christine Binquet, Élodie Gautier, Karin Mayer, Mine Arslan‐Kirchner, Maurizia Grasso, Christophe Béroud, Dalil Hamroun, Claire Bonithon‐Kopp, H Plauchu, Peter N. Robinson, Julie De Backer, Paul Coucke, Uta Francke, O. Bouchot, J. E. Wolf, Chantal Stheneur, Nadine Hanna, Delphine Détaint, Anne De Paepe, Cathérine Boileau, Guillaume Jondeau
出版事項 2011Artigo -
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Measurable residual disease monitoring in acute myeloid leukemia with t(8;21)(q22;q22.1): results from the AML Study Group 著者: Frank G. Rücker, Mridul Agrawal, Andrea Corbacioglu, Daniela Weber, Silke Kapp‐Schwoerer, Verena I. Gaidzik, Nikolaus Jahn, Thomas Schroeder, Mohammed Wattad, Michael Lübbert, Elisabeth Koller, Thomas Kindler, Katharina S. Götze, Mark Ringhoffer, Jörg Westermann, Walter Fiedler, Heinz A. Horst, Richard Greil, Roland Schroers, Karin Mayer, Thomas Heinicke, Jürgen Krauter, Richard F. Schlenk, Felicitas Thol, Michael Heuser, Arnold Ganser, Lars Bullinger, Peter Paschka, Hartmut Döhner, Konstanze Döhner
出版事項 2019Artigo
関連主題
Internal medicine
Medicine
Biology
Genetics
Gene
Oncology
Mutation
Surgery
Gastroenterology
Marfan syndrome
Pathology
Proband
Bone marrow
Intensive care medicine
Pediatrics
Cancer
Chemotherapy
Chromosome
Cumulative incidence
Hematology
Karyotype
Myeloid leukemia
Transplantation
Aorta
Aortic dissection
Biochemistry
Cancer research
Cardiology
Chemistry
Cohort