Zobrazeno 1 - 10
of 30
pro vyhledávání: '"Thomas Vraetz"'
Autor:
Magdolna Nagy, Tom G. Mastenbroek, Nadine J.A. Mattheij, Susanne de Witt, Kenneth J. Clemetson, Janbernd Kirschner, Ansgar S. Schulz, Thomas Vraetz, Carsten Speckmann, Attila Braun, Judith M.E.M. Cosemans, Barbara Zieger, Johan W.M. Heemskerk
Publikováno v:
Haematologica, Vol 103, Iss 3 (2018)
In patients with dysfunctions of the Ca2+ channel ORAI1, stromal interaction molecule 1 (STIM1) or integrin-regulating kindlin-3 (FERMT3), severe immunodeficiency is frequently linked to abnormal platelet activity. In this paper, we studied platelet
Externí odkaz:
https://doaj.org/article/20faddd9204141f5aae97088a73973aa
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:
Valeria Falcone, Marcus Panning, Brigitte Strahm, Thomas Vraetz, Sibylle Bierbaum, Dieter Neumann-Haefelin, Daniela Huzly
Publikováno v:
Emerging Infectious Diseases, Vol 18, Iss 4, Pp 706-708 (2012)
Externí odkaz:
https://doaj.org/article/7d802d7ac32d4e24be8a7026f00bc82e
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
Publikováno v:
JuKiP - Ihr Fachmagazin für Gesundheits- und Kinderkrankenpflege. :239-244
Zusammenfassung Vom Heilungserfolg wissenschaftsbasierter Architektur für Kinder- und Jugendkliniken Kann man Heilungs- und Entwicklungschancen hospitalisierter Kinder und Jugendlicher mittels Architektur verbessern? Noch nie wurde der Frage so kons
Autor:
Christian Klemann, Maximilian Heeg, Udo zur Stadt, Thomas Vraetz, Miriam Heizmann, Claudia Roll, Sebastian F. N. Bode, Klaus Schwarz, Stefan Feske, Hans Fuchs, Stephan Ehl, Sandra Ammann, Jan Rohr, Carsten Speckmann, Sebastian Fuchs, Myriam Ricarda Lorenz, Kai Lehmberg
Publikováno v:
Journal of Allergy and Clinical Immunology. 140:1721-1724
Autor:
Annick Lim, Nathalie Lambert, Christelle Lenoir, Anne Rensing-Ehl, Stephan Ehl, Carsten Speckmann, Sebastian Fuchs, Wilma Mannhardt-Laakmann, Klaus Schwarz, Wolfgang W. A. Schamel, Capucine Picard, Fabian Hauck, Britta Blumenthal, Marine Gil, Thomas Vraetz, Sylvain Latour, Alain Fischer, Stephan Borte, Marie Audrain, Emmanuel Martin
Publikováno v:
Clinical Immunology. 161:103-109
Autosomal recessive human ZAP70 deficiency is a rare cause of combined immunodeficiency (CID) characterized by defective CD4 T cells and profound CD8 T cell lymphopenia. Herein, we report two novel patients that extend the molecular genetics, the cli
Autor:
Despina Moshous, Manfred Hoenig, Alain Fischer, Mónica Martínez-Gallo, Sebastian Fuchs, Caterina Cancrini, Thomas Vraetz, Sujal Ghosh, Ansgar Schulz, Christine Winterhalter, Nikolaus Rieber, Andrew R. Gennery, Annette Uhlmann, Luis M. Allende, Andrew J. Cant, Kimberly Gilmour, Fabian Hauck, Alessia Scarselli, Brigitte Strahm, Tadej Avcin, Klaus Schwarz, Luigi D. Notarangelo, Tim Niehues, Carsten Speckmann, Alessandro Aiuti, Capucine Picard, H. Bobby Gaspar, Michael H. Albert, Klaus Warnatz, Pere Soler-Palacín, Polina Stepensky, Luis Ignacio Gonzalez-Granado, Stephan Ehl, Silvia Di Cesare, Sam Doerken, Andrea Finocchi, Bénédicte Neven, Sophie Hambleton, Waleed Al-Herz, Ruy Perez-Becker, Markus G. Seidel, Austen Worth
Publikováno v:
Repositorio Institucional de la Consejería de Sanidad de la Comunidad de Madrid
Consejería de Sanidad de la Comunidad de Madrid
Consejería de Sanidad de la Comunidad de Madrid
Background Absent T-cell immunity resulting in life-threatening infections provides a clear rationale for hematopoetic stem cell transplantation (HSCT) in patients with severe combined immunodeficiency (SCID). Combined immunodeficiencies (CIDs) and "
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1db8f0f84572820e12d3a2b4e64dfecd
http://hdl.handle.net/2108/234359
http://hdl.handle.net/2108/234359
Autor:
Ryuta Nishikomori, Rainer Doffinger, Beatriz Tavares Costa-Carvalho, Andrew R. Gennery, Shinya Sasaki, Erwin W. Gelfand, Shanmuganathan Chandrakasan, Tsubasa Okano, Alberto Olaya-Vargas, Paul Veys, Alfons Krol, Andrea M. Jones, Jean-Laurent Casanova, Etsuro Ito, Waseem Qasim, Thomas Vraetz, Jordan S. Orange, Estelle Colin, Marco Antonio Yamazaki-Nakashimada, Mario Abinun, Nyree Cole, Zeynep Yesim Kucuk, Tayfun Güngör, Chihaya Imai, Capucine Picard, Charline Miot, Steven M. Holland, Stéphane Blanche, Sara Espinosa Padilla, Isabelle Pellier, Despina Moshous, Benedicte Neven, Antonio Condino-Neto, Gulbu Uzel, Jana Pachlopnik Schmid, Smita Y. Patel, Kohsuke Imai, Jérémie Rosain, Jack J. Bleesing, Sophie Dupuis Girod, Stephan Ehl, Jacinta Bustamante, Anthony J. Mancini, Anne Puel, Tokomki Kawai, Stephen Jolles
Publikováno v:
Repositório Institucional da USP (Biblioteca Digital da Produção Intelectual)
Universidade de São Paulo (USP)
instacron:USP
Blood
Blood, American Society of Hematology, 2017, 130 (12), pp.1456-1467. ⟨10.1182/blood-2017-03-771600⟩
Universidade de São Paulo (USP)
instacron:USP
Blood
Blood, American Society of Hematology, 2017, 130 (12), pp.1456-1467. ⟨10.1182/blood-2017-03-771600⟩
International audience; X-linked recessive ectodermal dysplasia with immunodeficiency is a rare primary immunodeficiency caused by hypomorphic mutations of the gene encoding the nuclear factor κB essential modulator (NEMO) protein. This condition di
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2de5330d991630d1d83655fb0c9593e3
Autor:
Jan Soerensen, B. Rodeck, M. Fritsch, Thomas Vraetz, Brigitte Strahm, Bernd H. Belohradsky, Melchior Lauten, Klaus Schwarz, Myriam Ricarda Lorenz, Stephan Ehl, Ulrich Salzer, Michael H. Albert, Joerg J Meerpohl, Kai Lehmberg, Mads Gyrd-Hansen, Anne Rensing-Ehl, Ilka Fuchs, S. Schibli, R Kolb, Catherine M. Cale, Bodo Grimbacher, A Hassan, Heike Ufheil, Rune Busk Damgaard, H. von Bernuth, M. Elawad, Wolfgang Eberl, U zur Stadt, Carsten Speckmann, M. Kohl
X-linked inhibitor of apoptosis (XIAP) deficiency caused by mutations in BIRC4 was initially described in patients with X-linked lymphoproliferative syndrome (XLP) who had no mutations in SH2D1A. In the initial reports, EBV-associated hemophagocytic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9c5f6e19349e0826a3d9c800c24bd7a8
https://ora.ox.ac.uk/objects/uuid:c405643f-ce1b-425e-b7be-6fe573966d84
https://ora.ox.ac.uk/objects/uuid:c405643f-ce1b-425e-b7be-6fe573966d84