Editorial: Current Challenges in Immune and Other Acquired Cytopenias of Childhood

por Ghosh, Sujal, Seidel, Markus G.
Publicado 2016

The Pattern of Malignancies in Down Syndrome and Its Potential Context With the Immune System

por Satgé, Daniel, Seidel, Markus G.
Publicado 2018

Different Apples, Same Tree: Visualizing Current Biological and Clinical Insights into CTLA-4 Insufficiency and LRBA and DEF6 Deficiencies

por Gámez-Díaz, Laura, Seidel, Markus G.
Publicado 2021

Editorial: The Relationship Between Cancer Predisposition and Primary Immunodeficiency

por Hauck, Fabian, Gennery, Andrew R., Seidel, Markus G.
Publicado 2019

Allogeneic Hematopoietic Stem Cell Transplantation for Congenital Immune Dysregulatory Disorders

por Bakhtiar, Shahrzad, Fekadu, Julia, Seidel, Markus G., Gambineri, Eleonora
Publicado 2019

The Immune Deficiency and Dysregulation Activity (IDDA2.1 ‘Kaleidoscope’) Score and Other Clinical Measures in Inborn Errors of Immunity

por Seidel, Markus G., Tesch, Victoria K., Yang, Linlin, Hauck, Fabian, Horn, Anna Lena, Smolle, Maria Anna, Quehenberger, Franz, Benesch, Martin
Publicado 2021

Correction to: The Immune Deficiency and Dysregulation Activity (IDDA2.1 ‘Kaleidoscope’) Score and Other Clinical Measures in Inborn Errors of Immunity

por Seidel, Markus G., Tesch, Victoria K., Yang, Linlin, Hauck, Fabian, Horn, Anna Lena, Smolle, Maria Anna, Quehenberger, Franz, Benesch, Martin
Publicado 2022

Immune Thrombocytopenia in Two Unrelated Fanconi Anemia Patients – A Mere Coincidence?

por Karastaneva, Anna, Lanz, Sofia, Wawer, Angela, Behrends, Uta, Schindler, Detlev, Dietrich, Ralf, Burdach, Stefan, Urban, Christian, Benesch, Martin, Seidel, Markus G.
Publicado 2015

Clinical implementation of plasma cell-free circulating tumor DNA quantification by digital droplet PCR for the monitoring of Ewing sarcoma in children and adolescents

por Seidel, Markus G., Kashofer, Karl, Moser, Tina, Thueringer, Andrea, Liegl-Atzwanger, Bernadette, Leithner, Andreas, Szkandera, Joanna, Benesch, Martin, El-Heliebi, Amin, Heitzer, Ellen
Publicado 2022

The Phenotype and Treatment of WIP Deficiency: Literature Synopsis and Review of a Patient With Pre-transplant Serial Donor Lymphocyte Infusions to Eliminate CMV

por Schwinger, Wolfgang, Urban, Christian, Ulreich, Raphael, Sperl, Daniela, Karastaneva, Anna, Strenger, Volker, Lackner, Herwig, Boztug, Kaan, Albert, Michael H., Benesch, Martin, Seidel, Markus G.
Publicado 2018

Long-term remission after allogeneic hematopoietic stem cell transplantation in LPS-responsive beige-like anchor (LRBA) deficiency

por Seidel, Markus G., Hirschmugl, Tatjana, Gamez-Diaz, Laura, Schwinger, Wolfgang, Serwas, Nina, Deutschmann, Andrea, Gorkiewicz, Gregor, Zenz, Werner, Windpassinger, Christian, Grimbacher, Bodo, Urban, Christian, Boztug, Kaan
Publicado 2015

Malignancy and chemotherapy induced haemophagocytic lymphohistiocytosis in children and adolescents—a single centre experience of 20 years

por Strenger, Volker, Merth, Gerald, Lackner, Herwig, Aberle, Stephan W., Kessler, Harald H., Seidel, Markus G., Schwinger, Wolfgang, Sperl, Daniela, Sovinz, Petra, Karastaneva, Anna, Benesch, Martin, Urban, Christian
Publicado 2018

Nfil3/E4bp4 is required for the development and maturation of NK cells in vivo

por Kamizono, Shintaro, Duncan, Gordon S., Seidel, Markus G., Morimoto, Akira, Hamada, Koichi, Grosveld, Gerard, Akashi, Koichi, Lind, Evan F., Haight, Jillian P., Ohashi, Pamela S., Look, A. Thomas, Mak, Tak W.
Publicado 2009

Functional type 1 regulatory T cells develop regardless of FOXP3 mutations in patients with IPEX syndrome

por Passerini, Laura, Di Nunzio, Sara, Gregori, Silvia, Gambineri, Eleonora, Cecconi, Massimiliano, Seidel, Markus G, Cazzola, Giantonio, Perroni, Lucia, Tommasini, Alberto, Vignola, Silvia, Guidi, Luisa, Roncarolo, Maria G, Bacchetta, Rosa
Publicado 2011

A novel immunodeficiency syndrome associated with partial trisomy 19p13

por Seidel, Markus G, Duerr, Celia, Woutsas, Stavroula, Schwerin-Nagel, Anette, Sadeghi, Kambis, Neesen, Jürgen, Uhrig, Sabine, Santos-Valente, Elisangela, Pickl, Winfried F, Schwinger, Wolfgang, Urban, Christian, Boztug, Kaan, Förster-Waldl, Elisabeth
Publicado 2014

Current Understanding and Future Research Priorities in Malignancy Associated With Inborn Errors of Immunity and DNA Repair Disorders: The Perspective of an Interdisciplinary Worki...

por Bomken, Simon, van der Werff Ten Bosch, Jutte, Attarbaschi, Andishe, Bacon, Chris M., Borkhardt, Arndt, Boztug, Kaan, Fischer, Ute, Hauck, Fabian, Kuiper, Roland P., Lammens, Tim, Loeffen, Jan, Neven, Bénédicte, Pan-Hammarström, Qiang, Quinti, Isabella, Seidel, Markus G., Warnatz, Klaus, Wehr, Claudia, Lankester, Arjan C., Gennery, Andrew R.
Publicado 2018

No Overt Clinical Immunodeficiency Despite Immune Biological Abnormalities in Patients With Constitutional Mismatch Repair Deficiency

por Tesch, Victoria K., IJspeert, Hanna, Raicht, Andrea, Rueda, Daniel, Dominguez-Pinilla, Nerea, Allende, Luis M., Colas, Chrystelle, Rosenbaum, Thorsten, Ilencikova, Denisa, Baris, Hagit N., Nathrath, Michaela H. M., Suerink, Manon, Januszkiewicz-Lewandowska, Danuta, Ragab, Iman, Azizi, Amedeo A., Wenzel, Soeren S., Zschocke, Johannes, Schwinger, Wolfgang, Kloor, Matthias, Blattmann, Claudia, Brugieres, Laurence, van der Burg, Mirjam, Wimmer, Katharina, Seidel, Markus G.
Publicado 2018

Genotype–phenotype associations within the Li-Fraumeni spectrum: a report from the German Registry

por Penkert, Judith, Strüwe, Farina J., Dutzmann, Christina M., Doergeloh, Beate B., Montellier, Emilie, Freycon, Claire, Keymling, Myriam, Schlemmer, Heinz-Peter, Sänger, Birte, Hoffmann, Beatrice, Gerasimov, Tanja, Blattmann, Claudia, Fetscher, Sebastian, Frühwald, Michael, Hettmer, Simone, Kordes, Uwe, Ridola, Vita, Kroiss Benninger, Sabine, Mastronuzzi, Angela, Schott, Sarah, Nees, Juliane, Prokop, Aram, Redlich, Antje, Seidel, Markus G., Zimmermann, Stefanie, Pajtler, Kristian W., Pfister, Stefan M., Hainaut, Pierre, Kratz, Christian P.
Publicado 2022

A sensitive and scalable microsatellite instability assay to diagnose constitutional mismatch repair deficiency by sequencing of peripheral blood leukocytes

por Gallon, Richard, Mühlegger, Barbara, Wenzel, Sören‐Sebastian, Sheth, Harsh, Hayes, Christine, Aretz, Stefan, Dahan, Karin, Foulkes, William, Kratz, Christian P., Ripperger, Tim, Azizi, Amedeo A., Baris Feldman, Hagit, Chong, Anne‐Laure, Demirsoy, Ugur, Florkin, Benoît, Imschweiler, Thomas, Januszkiewicz‐Lewandowska, Danuta, Lobitz, Stephan, Nathrath, Michaela, Pander, Hans‐Jürgen, Perez‐Alonso, Vanesa, Perne, Claudia, Ragab, Iman, Rosenbaum, Thorsten, Rueda, Daniel, Seidel, Markus G., Suerink, Manon, Taeubner, Julia, Zimmermann, Stefanie‐Yvonne, Zschocke, Johannes, Borthwick, Gillian M., Burn, John, Jackson, Michael S., Santibanez‐Koref, Mauro, Wimmer, Katharina
Publicado 2019

Curation and expansion of Human Phenotype Ontology for defined groups of inborn errors of immunity

por Haimel, Matthias, Pazmandi, Julia, Heredia, Raú Jiménez, Dmytrus, Jasmin, Bal, Sevgi Köstel, Zoghi, Samaneh, van Daele, Paul, Briggs, Tracy A., Wouters, Carine, Bader-Meunier, Brigitte, Aeschlimann, Florence A., Caorsi, Roberta, Eleftheriou, Despina, Hoppenreijs, Esther, Salzer, Elisabeth, Bakhtiar, Shahrzad, Derfalvi, Beata, Saettini, Francesco, Kusters, Maaike A. A., Elfeky, Reem, Trück, Johannes, Rivière, Jacques G., van der Burg, Mirjam, Gattorno, Marco, Seidel, Markus G., Burns, Siobhan, Warnatz, Klaus, Hauck, Fabian, Brogan, Paul, Gilmour, Kimberly C., Schuetz, Catharina, Simon, Anna, Bock, Christoph, Hambleton, Sophie, de Vries, Esther, Robinson, Peter N., van Gijn, Marielle, Boztug, Kaan
Publicado 2022