Search Results - Maja Klaudel‐Dreszler
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1
Disseminated Bacillus Calmette-Guérin Infection and Immunodeficiency by Ewa Bernatowska, Beata Wolska‐Kuśnierz, Małgorzata Pac, Magdalena Kurenko-Deptuch, Zofia Zwolska, Jean‐Laurent Casanova, Barbara Piątosa, Jacques J. M. van Dongen, Kazimierz Roszkowski, Bożena Mikołuć, Maja Klaudel‐Dreszler, Anna Liberek
Published 2007Carta -
2
Genetic and clinical characteristics of patients with Shwachman Diamond syndrome with special consideration of treatment with granulocyte-colony stimulating factor by Sabine Mellor-Heineke, Julia Skokowa, Natali Gerschmann, Е. А. Деордиева, Ivan Tesakov, Sally E. Kinsey, Maja Klaudel‐Dreszler, Piero Farruggia, Martina Suková, Mikael Sundin, Yasmine El Chazli, Tania Nicole Masmas, Leen Willems, Georg Ebetsberger‐Dachs, Hans Christian Erichsen, Orna Steinberg‐Shemer, Anna Shcherbina, Karl Welte, Cornelia Zeidler
Published 2025Artigo -
3
Heterozygous <i>TBK1</i> mutations impair TLR3 immunity and underlie herpes simplex encephalitis of childhood by Melina Herman, Michael J. Ciancanelli, Yi-Hung Ou, Lazaro Lorenzo, Maja Klaudel‐Dreszler, Elodie Pauwels, Vanessa Sancho‐Shimizu, Rebeca Pérez de Diego, Avinash Abhyankar, Elisabeth Israelsson, Yiqi Guo, Annabelle Cardon, Flore Rozenberg, Pierre Lebon, Marc Tardieu, Edyta Heropolitańska–Pliszka, Damien Chaussabel, Michael A. White, Laurent Abel, Shen‐Ying Zhang, Jean‐Laurent Casanova
Published 2012Artigo -
4
Extended clinical phenotypes and treatment modalities in 32 JAGN1-deficient patients. A multicenter study by EBMT IEWP by Julia Fekadu-Siebald, Emilia Salzmann‐Manrique, Jan Robert Heusel, André Willasch, Fabian Hauck, Luis Ignacio González‐Granado, Zahra Chavoshzadeh, Samin Sharafian, Franziska Cuntz, Safa Barış, Andrea Finocchi, Mattia Algeri, Roya Sherkat, Maja Klaudel‐Dreszler, Cornelia Zeidler, Christine Bellanné‐Chantelot, Gerhard Kindle, Blandine Beaupain, Catherine Paillard, Markus G. Seidel, Peter Bader, Michael H. Albert, Bénédicte Neven, Jean Donadieu, Shahrzad Bakhtiar
Published 2025Artigo -
5
Human RIPK1 deficiency causes combined immunodeficiency and inflammatory bowel diseases by Yue Li, Marita Führer, Ehsan Bahrami, Piotr Socha, Maja Klaudel‐Dreszler, A. Bouzidi, Yanshan Liu, Anna S. Lehle, Thomas Magg, Sebastian Hollizeck, Meino Rohlfs, Raffaele Conca, Michael Field, Neil Warner, Mordechai Slae, Eyal Shteyer, Dan Turner, Rachida Boukari, Reda Belbouab, Christoph Walz, Moritz M. Gaidt, Veit Hornung, Bernd Baumann, Ulrich Pannicke, Eman Al Idrissi, Hamza AlGhamdi, Fernando E. Sepulveda, Marine Gil, Geneviève de Saint Basile, Manfred Hönig, Sibylle Koletzko, Aleixo M. Muise, Scott B. Snapper, Klaus Schwarz, Christoph Klein, Daniel Kotlarz
Published 2018Artigo
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