Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Timo Volk"'
Autor:
Jurik A. Mutter, Stefan K. Alig, Mohammad S. Esfahani, Eliza M. Lauer, Jan Mitschke, David M. Kurtz, Julia Kühn, Sabine Bleul, Mari Olsen, Chih Long Liu, Michael C. Jin, Charles W. Macaulay, Nicolas Neidert, Timo Volk, Michel Eisenblaetter, Sebastian Rauer, Dieter H. Heiland, Jürgen Finke, Justus Duyster, Julius Wehrle, Marco Prinz, Gerald Illerhaus, Peter C. Reinacher, Elisabeth Schorb, Maximilian Diehn, Ash A. Alizadeh, Florian Scherer
Publikováno v:
Journal of clinical oncology : official journal of the American Society of Clinical Oncology.
PURPOSE Clinical outcomes of patients with CNS lymphomas (CNSLs) are remarkably heterogeneous, yet identification of patients at high risk for treatment failure is challenging. Furthermore, CNSL diagnosis often remains unconfirmed because of contrain
Autor:
Klaus Warnatz, Gisela Schluh, Sebastian Rauer, Reinhard Marks, Jessica Rojas-Restrepo, Horst Urbach, Bodo Grimbacher, Timo Volk, Valentina Strohmeier
Publikováno v:
Journal of Neurology
Progressive multifocal leukoencephalopathy is a rare opportunistic infection of the brain by John Cunningham polyomavirus in immune-compromised patients. In cases where no overt option for immune reconstitution is available [e.g., in patients with pr
Autor:
Jurik Andreas Mutter, Stefan Alig, Eliza Maria Lauer, Mohammad Shahrokh Esfahani, Jan Mitschke, David M. Kurtz, Julia Kühn, Sabine Bleul, Mari Olsen, Chih Long Liu, Michael C. Jin, Charles Macaulay, Nicolas Noel Neidert, Timo Volk, Sebastian Rauer, Dieter Henrik Heiland, Jürgen Finke, Justus Duyster, Julius Wehrle, Marco Prinz, Gerald Illerhaus, Peter C. Reinacher, Elisabeth Schorb, Maximilian Diehn, Ash A. Alizadeh, Florian Scherer
Publikováno v:
Blood. 138:6-6
Introduction: Clinical outcomes for patients with central nervous system lymphoma (CNSL) are remarkably heterogeneous, yet identification of patients at high risk for treatment failure remains challenging with existing methods. In addition, diagnosis
Autor:
Ulrich Salzer, Paul Fisch, Marta Rizzi, Ulrich Pannicke, Michael Hummel, Klaus Schwarz, Hongzhi Cao, Sevgi Keles, Bodo Grimbacher, Michela Di Virgilio, Julia Ritter, Dietmar Pfeifer, Alla Bulashevska, Lennart Hammarstrom, Qiang Pan-Hammarström, Esra Hazar Sayar, Detlev Schindler, Alejandro A. Schäffer, Andrea Björkman, Ismail Reisli, Manfred Fliegauf, Zafer Caliskaner, S¸ükrü Güner, Timo Volk, Karin Zimmermann, Fang Yang
Publikováno v:
Human Molecular Genetics. 24:7361-7372
Null mutations in genes involved in V(D)J recombination cause a block in B- and T-cell development, clinically presenting as severe combined immunodeficiency (SCID). Hypomorphic mutations in the non-homologous end-joining gene DCLRE1C (encoding ARTEM
Autor:
Hendrik-Tobias Arkenau, Emiliano Calvo, Alain Mita, Young Kwang Chae, Devalingam Mahalingam, Ugur Sahin, Elena Garralda, Oezlem Tuereci, Vladimir Galvao, Stefan Symeonides, Maria Miguel, Hariz Hassan, Annette Baumhauer, Timo Völker, Marie-Cristine Kühnle, Roman Rösemann, Stefan Strobl
Publikováno v:
Journal for ImmunoTherapy of Cancer, Vol 9, Iss Suppl 2 (2021)
Externí odkaz:
https://doaj.org/article/f934ebca1c46480bbd8a10a2221a40bb