Zobrazeno 1 - 10
of 21
pro vyhledávání: '"Ute Gross-Wieltsch"'
Autor:
Sabine M. El-Helou, Anika-Kerstin Biegner, Sebastian Bode, Stephan R. Ehl, Maximilian Heeg, Maria E. Maccari, Henrike Ritterbusch, Carsten Speckmann, Stephan Rusch, Raphael Scheible, Klaus Warnatz, Faranaz Atschekzei, Renata Beider, Diana Ernst, Stev Gerschmann, Alexandra Jablonka, Gudrun Mielke, Reinhold E. Schmidt, Gesine Schürmann, Georgios Sogkas, Ulrich H. Baumann, Christian Klemann, Dorothee Viemann, Horst von Bernuth, Renate Krüger, Leif G. Hanitsch, Carmen M. Scheibenbogen, Kirsten Wittke, Michael H. Albert, Anna Eichinger, Fabian Hauck, Christoph Klein, Anita Rack-Hoch, Franz M. Sollinger, Anne Avila, Michael Borte, Stephan Borte, Maria Fasshauer, Anja Hauenherm, Nils Kellner, Anna H. Müller, Anett Ülzen, Peter Bader, Shahrzad Bakhtiar, Jae-Yun Lee, Ursula Heß, Ralf Schubert, Sandra Wölke, Stefan Zielen, Sujal Ghosh, Hans-Juergen Laws, Jennifer Neubert, Prasad T. Oommen, Manfred Hönig, Ansgar Schulz, Sandra Steinmann, Klaus Schwarz, Gregor Dückers, Beate Lamers, Vanessa Langemeyer, Tim Niehues, Sonu Shai, Dagmar Graf, Carmen Müglich, Marc T. Schmalzing, Eva C. Schwaneck, Hans-Peter Tony, Johannes Dirks, Gabriele Haase, Johannes G. Liese, Henner Morbach, Dirk Foell, Antje Hellige, Helmut Wittkowski, Katja Masjosthusmann, Michael Mohr, Linda Geberzahn, Christian M. Hedrich, Christiane Müller, Angela Rösen-Wolff, Joachim Roesler, Antje Zimmermann, Uta Behrends, Nikolaus Rieber, Uwe Schauer, Rupert Handgretinger, Ursula Holzer, Jörg Henes, Lothar Kanz, Christoph Boesecke, Jürgen K. Rockstroh, Carolynne Schwarze-Zander, Jan-Christian Wasmuth, Dagmar Dilloo, Brigitte Hülsmann, Stefan Schönberger, Stefan Schreiber, Rainald Zeuner, Tobias Ankermann, Philipp von Bismarck, Hans-Iko Huppertz, Petra Kaiser-Labusch, Johann Greil, Donate Jakoby, Andreas E. Kulozik, Markus Metzler, Nora Naumann-Bartsch, Bettina Sobik, Norbert Graf, Sabine Heine, Robin Kobbe, Kai Lehmberg, Ingo Müller, Friedrich Herrmann, Gerd Horneff, Ariane Klein, Joachim Peitz, Nadine Schmidt, Stefan Bielack, Ute Groß-Wieltsch, Carl F. Classen, Jessica Klasen, Peter Deutz, Dirk Kamitz, Lisa Lassay, Klaus Tenbrock, Norbert Wagner, Benedikt Bernbeck, Bastian Brummel, Eusebia Lara-Villacanas, Esther Münstermann, Dominik T. Schneider, Nadine Tietsch, Marco Westkemper, Michael Weiß, Christof Kramm, Ingrid Kühnle, Silke Kullmann, Hermann Girschick, Christof Specker, Elisabeth Vinnemeier-Laubenthal, Henriette Haenicke, Claudia Schulz, Lothar Schweigerer, Thomas G. Müller, Martina Stiefel, Bernd H. Belohradsky, Veronika Soetedjo, Gerhard Kindle, Bodo Grimbacher
Publikováno v:
Frontiers in Immunology, Vol 10 (2019)
Introduction: The German PID-NET registry was founded in 2009, serving as the first national registry of patients with primary immunodeficiencies (PID) in Germany. It is part of the European Society for Immunodeficiencies (ESID) registry. The primary
Externí odkaz:
https://doaj.org/article/e9075140b79b4c8c90ad31f540d2800a
Autor:
Sebastian FN Bode, Sandra Ammann, Waleed Al-Herz, Mihaela Bataneant, Christopher C Dvorak, Stephan Gehring, Andrew Gennery, Kimberly C Gilmour, Luis I Gonzalez-Granado, Ute Groß-Wieltsch, Marianne Ifversen, Jenny Lingman-Framme, Susanne Matthes-Martin, Rolf Mesters, Isabelle Meyts, Joris M van Montfrans, Jana Pachlopnik Schmid, Sung-Yun Pai, Pere Soler-Palacin, Uta Schuermann, Volker Schuster, Markus G. Seidel, Carsten Speckmann, Polina Stepensky, Karl-Walter Sykora, Bianca Tesi, Thomas Vraetz, Catherine Waruiru, Yenan T. Bryceson, Despina Moshous, Kai Lehmberg, Michael B Jordan, Stephan Ehl
Publikováno v:
Haematologica, Vol 100, Iss 7 (2015)
Hemophagocytic lymphohistiocytosis is a hyperinflammatory syndrome defined by clinical and laboratory criteria. Current criteria were created to identify patients with familial hemophagocytic lmyphohistiocytosis in immediate need of immunosuppressive
Externí odkaz:
https://doaj.org/article/b94f214e81d0465d86266c06df2efdde
Autor:
Jan Rohr, Karin Beutel, Andrea Maul-Pavicic, Thomas Vraetz, Jens Thiel, Klaus Warnatz, Ilka Bondzio, Ute Gross-Wieltsch, Michael Schündeln, Barbara Schütz, Wilhelm Woessmann, Andreas H. Groll, Brigitte Strahm, Julia Pagel, Carsten Speckmann, Gritta Janka, Gillian Griffiths, Klaus Schwarz, Udo zur Stadt, Stephan Ehl
Publikováno v:
Haematologica, Vol 95, Iss 12 (2010)
Background Familial hemophagocytic lymphohistiocytosis is a genetic disorder of lymphocyte cytotoxicity that usually presents in the first two years of life and has a poor prognosis unless treated by hematopoietic stem cell transplantation. Atypical
Externí odkaz:
https://doaj.org/article/011b5e64da624c7c934bd9291ccfa495
Autor:
Ayami Yoshimi, Irith Baumann, Monika Führer, Eva Bergsträsser, Ulrich Göbel, Karl-Walter Sykora, Thomas Klingebiel, Ute Gross-Wieltsch, Marry M van den Heuvel-Eibrink, Alexandra Fischer, Peter Nöllke, Charlotte Niemeyer
Publikováno v:
Haematologica, Vol 92, Iss 3 (2007)
It is currently unknown whether immunosuppressive therapy or hematopoietic stem cell transplantation is the most appropriate treatment strategy for children with refractory cytopenia and normal karyotype or trisomy 8. We report on 31 children with hy
Externí odkaz:
https://doaj.org/article/9129bf78b6384d6fb2101725fbe05ace
Autor:
Thomas Lücke, Charlotte M. Niemeyer, Markus Metzler, Ayami Yoshimi, Kirsten Timmermann, Irene Schmid, Udo Kontny, Helen S Odenthal, Holger Cario, Aron Fisch, Alexander Hohnecker, Arndt Borkhardt, Daniela Karall, Gabriele Strauß, Ute Gross-Wieltsch, Stephan Lobitz, Tanja Höll, Barbara Uetz, Agnès Rötig, Sarah C. Grünert
Publikováno v:
British Journal of Haematology. 193:1283-1287
Autor:
Fabian Hauck, Ute Gross-Wieltsch, Ales Janda, Christian Stirnkorb, Julia Eilenberger, Fabian Glowatzki, Thekla von Kalle, Toni Hospach, Friederike Blankenburg
Publikováno v:
Arthritis und Rheuma. 40:124-126
Autor:
Michael C. Frühwald, Hermann Full, Dani Hakimeh, Aram Prokop, Miriam Erlacher, Irini Karapanagiotou-Schenkel, Christina Linke, Alexander Claviez, Dorothea Beck, Joachim B. Kunz, Laura Tagliaferri, Lena Oevermann, Andrea Jarisch, Lisa-Marie Rother, Wolfgang Eberl, Harald Reinhard, Pierre Allard, Selim Corbacioglu, Sabine Heine, Lucian Le Cornet, Andreas E. Kulozik, Martin Ebinger, Holger Cario, Matthias Dürken, Regine Grosse, Rita Beier, Claudia Khurana, Ute Groß-Wieltsch, Dominik Schneider, Stephan Lobitz, Markus Metzler, Daniela Schenk, Thomas Wiesel
Background Limited data on the prevalence and medical care of sickle cell disease (SCD) in Germany are available. Here, we make use of a patient registry to characterize the burden of disease and the treatment modalities for patients with SCD in Germ
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::196a57a77f4b3422032703f4d69c2ff8
https://opus.bibliothek.uni-augsburg.de/opus4/files/72205/pbc.28130.pdf
https://opus.bibliothek.uni-augsburg.de/opus4/files/72205/pbc.28130.pdf
Autor:
Arndt Borkhardt, Birgitte Lausen, Bernhard Kremens, Christian Thiede, Philipp Schulze, Angelika Eggert, Christina Nowasz, Adriana Balduzzi, Sabina Sufliarska, Olga Aleinikova, Petr Sedlacek, Gudrun Göhring, Gabriele Strauss, Frank Berthold, Günter Henze, Andreas H. Groll, Alexander Claviez, Brigitte Schlegelberger, Jochen Harbott, Ingmar Glauche, Hans Kreipe, Ute Groß-Wieltsch, Martin Schrappe, Josephine T. Tauer, Manuela Krumbholz, Eveline S. J. M. de Bont, Christoph Klein, Nils von Neuhoff, Markus Metzler, Andreas E. Kulozik, Karl Walter Sykora, Meinolf Suttorp
A total of 156 patients (age range 1.3-18.0 years, median 13.2 years; 91 (58.3%) male) with newly diagnosed CML (N = 146 chronic phase (CML-CP), N = 3 accelerated phase (CML-AP), N = 7 blastic phase (CML-BP)) received imatinib up-front (300, 400, 500
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b610d155c037bebf511185e42e3f5600
https://www.ncbi.nlm.nih.gov/pubmed/29925908
https://www.ncbi.nlm.nih.gov/pubmed/29925908
Autor:
Ayami Yoshimi, Kyogo Suzuki, Miriam Erlacher, Udo Kontny, Daniela Karall, Charlotte M. Niemeyer, Sarah C. Grünert, Stephan Lobitz, Holger Cario, Helen Wagner, Peter Noellke, Irene Schmid, Ute Gross-Wieltsch, Arndt Borkhardt
Publikováno v:
Blood. 134:3746-3746
Introduction: Pearson syndrome (PS) was originally reported as a sideroblastic anemia in infancy with vacuolization of marrow precursors and exocrine pancreas dysfunction. It is now recognized as a fatal multisystem mitochondrial disorder caused by s
Autor:
M Suttorp, Marry M. van den Heuvel-Eibrink, Andreas E. Kulozik, Ayami Yoshimi, Michael Dworzak, Annamaria Cseh, Lale Olcay, Ingrid Furlan, Andrea Candás, Franco Locatelli, Charlotte M. Niemeyer, Brigitte Strahm, Henrik Hasle, Riccardo Masetti, Christian Flotho, Ute Groß-Wieltsch, Markus Schmugge
Publikováno v:
Blood, 125(14), 2311-2313. American Society of Hematology
Cseh, A, Niemeyer, C M, Yoshimi, A, Dworzak, M, Hasle, H, van den Heuvel-Eibrink, M M, Locatelli, F, Masetti, R, Schmugge, M, Groß-Wieltsch, U, Candás, A, Kulozik, A E, Olcay, L, Suttorp, M, Furlan, I, Strahm, B & Flotho, C 2015, ' Bridging to transplant with azacitidine in juvenile myelomonocytic leukemia : a retrospective analysis of the EWOG-MDS study group ', Blood, vol. 125, no. 14, pp. 2311-3 . https://doi.org/10.1182/blood-2015-01-619734
Cseh, A, Niemeyer, C M, Yoshimi, A, Dworzak, M, Hasle, H, van den Heuvel-Eibrink, M M, Locatelli, F, Masetti, R, Schmugge, M, Groß-Wieltsch, U, Candás, A, Kulozik, A E, Olcay, L, Suttorp, M, Furlan, I, Strahm, B & Flotho, C 2015, ' Bridging to transplant with azacitidine in juvenile myelomonocytic leukemia : a retrospective analysis of the EWOG-MDS study group ', Blood, vol. 125, no. 14, pp. 2311-3 . https://doi.org/10.1182/blood-2015-01-619734
To the editor: DNA methyltransferase-inhibiting azanucleosides have become a mainstay of treatment of myeloid neoplasms in adult patients,[1][1] with 5-azacytidine (azacitidine) being the agent in broadest clinical use. Although not curative, treatme