Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Astrid Bergbreiter"'
Autor:
Titus J. Brinker, Achim Hekler, Alexander H. Enk, Joachim Klode, Axel Hauschild, Carola Berking, Bastian Schilling, Sebastian Haferkamp, Dirk Schadendorf, Tim Holland-Letz, Jochen S. Utikal, Christof von Kalle, Wiebke Ludwig-Peitsch, Judith Sirokay, Lucie Heinzerling, Magarete Albrecht, Katharina Baratella, Lena Bischof, Eleftheria Chorti, Anna Dith, Christina Drusio, Nina Giese, Emmanouil Gratsias, Klaus Griewank, Sandra Hallasch, Zdenka Hanhart, Saskia Herz, Katja Hohaus, Philipp Jansen, Finja Jockenhöfer, Theodora Kanaki, Sarah Knispel, Katja Leonhard, Anna Martaki, Liliana Matei, Johanna Matull, Alexandra Olischewski, Maximilian Petri, Jan-Malte Placke, Simon Raub, Katrin Salva, Swantje Schlott, Elsa Sody, Nadine Steingrube, Ingo Stoffels, Selma Ugurel, Anne Zaremba, Christoffer Gebhardt, Nina Booken, Maria Christolouka, Kristina Buder-Bakhaya, Therezia Bokor-Billmann, Alexander Enk, Patrick Gholam, Holger Hänßle, Martin Salzmann, Sarah Schäfer, Knut Schäkel, Timo Schank, Ann-Sophie Bohne, Sophia Deffaa, Katharina Drerup, Friederike Egberts, Anna-Sophie Erkens, Benjamin Ewald, Sandra Falkvoll, Sascha Gerdes, Viola Harde, Marion Jost, Katja Kosova, Laetitia Messinger, Malte Metzner, Kirsten Morrison, Rogina Motamedi, Anja Pinczker, Anne Rosenthal, Natalie Scheller, Thomas Schwarz, Dora Stölzl, Federieke Thielking, Elena Tomaschewski, Ulrike Wehkamp, Michael Weichenthal, Oliver Wiedow, Claudia Maria Bär, Sophia Bender-Säbelkampf, Marc Horbrügger, Ante Karoglan, Luise Kraas, Jörg Faulhaber, Cyrill Geraud, Ze Guo, Philipp Koch, Miriam Linke, Nolwenn Maurier, Verena Müller, Benjamin Thomas, Jochen Sven Utikal, Ali Saeed M. Alamri, Andrea Baczako, Matthias Betke, Carolin Haas, Daniela Hartmann, Markus V. Heppt, Katharina Kilian, Sebastian Krammer, Natalie Lidia Lapczynski, Sebastian Mastnik, Suzan Nasifoglu, Cristel Ruini, Elke Sattler, Max Schlaak, Hans Wolff, Birgit Achatz, Astrid Bergbreiter, Konstantin Drexler, Monika Ettinger, Anna Halupczok, Marie Hegemann, Verena Dinauer, Maria Maagk, Marion Mickler, Biance Philipp, Anna Wilm, Constanze Wittmann, Anja Gesierich, Valerie Glutsch, Katrin Kahlert, Andreas Kerstan, Philipp Schrüfer
Publikováno v:
European journal of cancer (Oxford, England : 1990). 113
Background Recent studies have successfully demonstrated the use of deep-learning algorithms for dermatologist-level classification of suspicious lesions by the use of excessive proprietary image databases and limited numbers of dermatologists. For t
Autor:
Astrid Bergbreiter, Ulrich Salzer
Publikováno v:
Humoral Primary Immunodeficiencies ISBN: 9783319917849
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::19f6c78b47e6489b4d7a39436eae26d2
https://doi.org/10.1007/978-3-319-91785-6_9
https://doi.org/10.1007/978-3-319-91785-6_9
Autor:
Titus J. Brinker, Achim Hekler, Alexander H. Enk, Joachim Klode, Axel Hauschild, Carola Berking, Bastian Schilling, Sebastian Haferkamp, Dirk Schadendorf, Stefan Fröhling, Jochen S. Utikal, Christof von Kalle, Wiebke Ludwig-Peitsch, Judith Sirokay, Lucie Heinzerling, Magarete Albrecht, Katharina Baratella, Lena Bischof, Eleftheria Chorti, Anna Dith, Christina Drusio, Nina Giese, Emmanouil Gratsias, Klaus Griewank, Sandra Hallasch, Zdenka Hanhart, Saskia Herz, Katja Hohaus, Philipp Jansen, Finja Jockenhöfer, Theodora Kanaki, Sarah Knispel, Katja Leonhard, Anna Martaki, Liliana Matei, Johanna Matull, Alexandra Olischewski, Maximilian Petri, Jan-Malte Placke, Simon Raub, Katrin Salva, Swantje Schlott, Elsa Sody, Nadine Steingrube, Ingo Stoffels, Selma Ugurel, Wiebke Sondermann, Anne Zaremba, Christoffer Gebhardt, Nina Booken, Maria Christolouka, Kristina Buder-Bakhaya, Therezia Bokor-Billmann, Alexander Enk, Patrick Gholam, Holger Hänßle, Martin Salzmann, Sarah Schäfer, Knut Schäkel, Timo Schank, Ann-Sophie Bohne, Sophia Deffaa, Katharina Drerup, Friederike Egberts, Anna-Sophie Erkens, Benjamin Ewald, Sandra Falkvoll, Sascha Gerdes, Viola Harde, Marion Jost, Katja Kosova, Laetitia Messinger, Malte Metzner, Kirsten Morrison, Rogina Motamedi, Anja Pinczker, Anne Rosenthal, Natalie Scheller, Thomas Schwarz, Dora Stölzl, Federieke Thielking, Elena Tomaschewski, Ulrike Wehkamp, Michael Weichenthal, Oliver Wiedow, Claudia Maria Bär, Sophia Bender-Säbelkampf, Marc Horbrügger, Ante Karoglan, Luise Kraas, Jörg Faulhaber, Cyrill Geraud, Ze Guo, Philipp Koch, Miriam Linke, Nolwenn Maurier, Verena Müller, Benjamin Thomas, Jochen Sven Utikal, Ali Saeed M. Alamri, Andrea Baczako, Matthias Betke, Carolin Haas, Daniela Hartmann, Markus V. Heppt, Katharina Kilian, Sebastian Krammer, Natalie Lidia Lapczynski, Sebastian Mastnik, Suzan Nasifoglu, Cristel Ruini, Elke Sattler, Max Schlaak, Hans Wolff, Birgit Achatz, Astrid Bergbreiter, Konstantin Drexler, Monika Ettinger, Anna Halupczok, Marie Hegemann, Verena Dinauer, Maria Maagk, Marion Mickler, Biance Philipp, Anna Wilm, Constanze Wittmann, Anja Gesierich, Valerie Glutsch, Katrin Kahlert, Andreas Kerstan, Philipp Schrüfer
Publikováno v:
European journal of cancer (Oxford, England : 1990). 111
Background: Recent studies have demonstrated the use of convolutional neural networks (CNNs) to classify images of melanoma with accuracies comparable to those achieved by board-certified dermatologists. However, the performance of a CNN exclusively
Autor:
Stephan Schreml, Christoph Brochhausen, Julia Schreml, Torsten E. Reichert, Ulrich Salzer, Tobias Ettl, Astrid Bergbreiter, Manfred Fliegauf, Yorick Söder, Teresa Jaeger, Andreas Redel, Antje Karle, Diane Bitzinger, Herbert Jägle, Reiner Neu, Mark Berneburg, Gerrit Spanier, Matthias Evert
Publikováno v:
European Journal of Medical Genetics. 64:104144
Background Mutations in NFKB1(nuclear factor of kappa light polypeptide gene enhancer in B-cells 1) are associated with a variety of clinical symptoms, including lymphadenopathy, splenomegaly, hepatomegaly, autoimmune haemolytic anaemia, arthralgia,
Autor:
Simon Urschel, Daniel Suez, Hans D. Ochs, Sanja Ugrinovic, Stephanie Jennings, Lennart Hammarström, Hans-Hartmut Peter, Tina Hagena, Alessandro Plebani, Are Martin Holm, Bodo Grimbacher, Tatiana C. Lawrence, Andrew McLean-Tooke, Chiara Bacchelli, Sylvie Buckridge, Alejandro A. Schäffer, A. David B. Webster, Stephanie Anover-Sombke, H. Bobby Gaspar, Qiang Pan-Hammarström, Dinakantha S. Kumararatne, Gavin P. Spickett, Helen Chapel, Bernd H. Belohradsky, Adrian J. Thrasher, Astrid Bergbreiter, Pascal Schneider, E. Michael Gertz, Jennifer Birmelin, Ulrich Salzer, Vassilis Lougaris, José Luis Franco, Ilka Schulze
Publikováno v:
Repositório Institucional da UNIFESP
Universidade Federal de São Paulo (UNIFESP)
instacron:UNIFESP
Blood; Vol 113
Universidade Federal de São Paulo (UNIFESP)
instacron:UNIFESP
Blood; Vol 113
Deutsche Forschungsgemeinschaft (Bonn, Germany) European Commission (Brussels, Belgium) National Institutes of Health/National Institute of Allergy and Infectious Diseases Primary Immunodeficiency Association (PIA; London, United Kingdom) Medical Res
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::037778eb9caab3f43f1cbeb6c580290b
https://doi.org/10.1182/blood-2008-02-141937
https://doi.org/10.1182/blood-2008-02-141937
Autor:
Astrid Bergbreiter, Javad Mohammadi, Mostafa Moin, Qiang Pan-Hammarström, Lennart Hammarström, Likun Du, Chonghai Liu, Asghar Aghamohammadi, Jiayi Lu, Ali Akbar Amirzargar, Nima Rezaei, Ulrich Salzer
Publikováno v:
Journal of Clinical Immunology. 29:777-785
Common variable immunodeficiency (CVID) is a heterogeneous syndrome characterized by impaired immunoglobulin production. The disorder is also characterized by co-occurrence of autoimmune, lymphoproliferative, and granulomatous diseases. Mutations in
Autor:
Athina Ganner, Haribaskar Ramachandran, Christian Mattonet, Gerd Walz, Martin Gerner, John A. Sayer, Peter G. Czarnecki, Albrecht Kramer-Zucker, Soeren S. Lienkamp, Astrid Bergbreiter, Tobias Schäfer, Edgar A. Otto, Michael Pütz, Friedhelm Hildebrandt, Verena Gieloff
Publikováno v:
Human Molecular Genetics. 17:3655-3662
Nephronophthisis (NPHP) is an autosomal recessive cystic kidney disease, caused by mutations of at least nine different genes. Several extrarenal manifestations characterize this disorder, including cerebellar defects, situs inversus and retinitis pi
Autor:
Astrid Bergbreiter, Ulrich Salzer
Publikováno v:
Expert review of clinical immunology. 5(2)
Common variable immunodeficiencies (CVIDs) encompass a heterogeneous group of disorders characterized by hypogammaglobulinemia, recurrent infections and a variety of sequelae. Recently, genetic defects in ICOS, TACI, CD19, Msh5 and BAFF-R have been a
Autor:
Marta Rizzi, Ulrich Salzer, Anne-Kathrin Kienzler, Jonathan P. Hannan, Dirk Lebrecht, Magdalena Grudzien, Lucas M. Kimmig, Bodo Grimbacher, Hans-Hartmut Peter, Tina Hagena, Stephanie Jennings, Nadine Völxen, Michael Schlesier, J. Thiel, J. A. Rump, Klaus Warnatz, Sylvia Gutenberger, Harald Illges, Ruth Draeger, Hermann Eibel, Annette Aichem, Astrid Bergbreiter
Publikováno v:
Journal of Allergy and Clinical Immunology. 129:801-810.e6
Background Complement receptor 2 (CR2/CD21) is part of the B-cell coreceptor and expressed by mature B cells and follicular dendritic cells. CD21 is a receptor for C3d-opsonized immune complexes and enhances antigen-specific B-cell responses. Objecti