Canlyniadau Chwilio - Hauck, Fabian
- Dangos 1 - 20 canlyniadau o 38
- Ewch i'r Dudalen Nesaf
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Epstein–Barr Virus(+) Smooth Muscle Tumors as Manifestation of Primary Immunodeficiency Disorders gan Magg, Thomas, Schober, Tilmann, Walz, Christoph, Ley-Zaporozhan, Julia, Facchetti, Fabio, Klein, Christoph, Hauck, Fabian
Cyhoeddwyd 2018Text -
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Lineage-Specific Chimerism and Outcome After Hematopoietic Stem Cell Transplantation for DOCK8 Deficiency gan Raedler, Johannes, Magg, Thomas, Rohlfs, Meino, Klein, Christoph, Vallée, Tanja, Hauck, Fabian, Albert, Michael H.
Cyhoeddwyd 2021Text -
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The Immune Deficiency and Dysregulation Activity (IDDA2.1 ‘Kaleidoscope’) Score and Other Clinical Measures in Inborn Errors of Immunity gan Seidel, Markus G., Tesch, Victoria K., Yang, Linlin, Hauck, Fabian, Horn, Anna Lena, Smolle, Maria Anna, Quehenberger, Franz, Benesch, Martin
Cyhoeddwyd 2021Text -
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Correction to: The Immune Deficiency and Dysregulation Activity (IDDA2.1 ‘Kaleidoscope’) Score and Other Clinical Measures in Inborn Errors of Immunity gan Seidel, Markus G., Tesch, Victoria K., Yang, Linlin, Hauck, Fabian, Horn, Anna Lena, Smolle, Maria Anna, Quehenberger, Franz, Benesch, Martin
Cyhoeddwyd 2022Text -
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T-cell replete haploidentical bone marrow transplantation and post-transplant cyclophosphamide for patients with inborn errors gan Kurzay, Mathias, Hauck, Fabian, Schmid, Irene, Wiebking, Volker, Eichinger, Anna, Jung, Eva, Boekstegers, Ann, Feuchtinger, Tobias, Klein, Christoph, Albert, Michael H.
Cyhoeddwyd 2019Text -
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Salvage HLA-haploidentical hematopoietic stem cell transplantation with post-transplant cyclophosphamide for graft failure in non-malignant disorders gan Albert, Michael H., Sirin, Mehtap, Hoenig, Manfred, Hauck, Fabian, Schuetz, Catharina, Bhattacharyya, Rajat, Stepensky, Polina, Jacoby, Elad, Güngör, Tayfun, Beier, Rita, Schulz, Ansgar
Cyhoeddwyd 2021Text -
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Outcomes for Nitazoxanide Treatment in a Case Series of Patients with Primary Immunodeficiencies and Rubella Virus Associated Granuloma gan Perelygina, Ludmila, Buchbinder, David, Dorsey, Morna J., Eloit, Marc, Hauck, Fabian, Hautala, Timo, Moshous, Despina, Uriarte, Ignacio, Deripapa, Elena, Icenogle, Joseph, Sullivan, Kathleen E
Cyhoeddwyd 2019Text -
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An Integrated clinical pathway for diagnosis, treatment and care of rare diseases: model, operating procedures, and results of the project TRANSLATE-NAMSE funded by the German Fede... gan Choukair, Daniela, Hauck, Fabian, Bettendorf, Markus, Krude, Heiko, Klein, Christoph, Bäumer, Tobias, Berner, Reinhard, Lee-Kirsch, Min Ae, Grasemann, Corinna, Burgard, Peter, Hoffmann, Georg F.
Cyhoeddwyd 2021Text -
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Scoping review of biological treatment of deficiency of interleukin-36 receptor antagonist (DITRA) in children and adolescents gan Hospach, Toni, Glowatzki, Fabian, Blankenburg, Friederike, Conzelmann, Dennis, Stirnkorb, Christian, Müllerschön, Chris Sandra, von den Driesch, Peter, Köhler, Lisa Maria, Rohlfs, Meino, Klein, Christoph, Hauck, Fabian
Cyhoeddwyd 2019Text -
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SARS-CoV-2 triggering severe ARDS and secondary HLH in a 3-year-old child with Down syndrome gan Kim-Hellmuth, Sarah, Hermann, Matthias, Eilenberger, Julia, Ley-Zaporozhan, Julia, Fischer, Marcus, Hauck, Fabian, Klein, Christoph, Haas, Nikolaus, Kappler, Matthias, Huebner, Johannes, Jakob, André, von Both, Ulrich
Cyhoeddwyd 2020Text -
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The Neurokinin-1 Receptor Is a Target in Pediatric Rhabdoid Tumors gan Kolorz, Julian, Demir, Salih, Gottschlich, Adrian, Beirith, Iris, Ilmer, Matthias, Lüthy, Daniel, Walz, Christoph, Dorostkar, Mario M., Magg, Thomas, Hauck, Fabian, von Schweinitz, Dietrich, Kobold, Sebastian, Kappler, Roland, Berger, Michael
Cyhoeddwyd 2021Text -
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A Novel Complete Autosomal-Recessive STAT1 LOF Variant Causes Immunodeficiency with Hemophagocytic Lymphohistiocytosis–Like Hyperinflammation gan Boehmer, Daniel F.R., Koehler, Lisa M., Magg, Thomas, Metzger, Philipp, Rohlfs, Meino, Ahlfeld, Julia, Rack-Hoch, Anita, Reiter, Karl, Albert, Michael H., Endres, Stefan, Rothenfusser, Simon, Klein, Christoph, Koenig, Lars M., Hauck, Fabian
Cyhoeddwyd 2020Text -
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Common Variable Immune Deficiency, Autoimmune Hemolytic Anemia and Pancytopenia associated with a Defect in IKAROS gan YILMAZ, Ebru, KUEHN, Hye Sun, ODAKIR, Eda, NIEMELA, Julie E., OZCAN, Alper, EKEN, Ahmet, ROHLFS, Meino, CANSEVER, Murat, GOK, Veysel, AYDIN, Firdevs, KARAKUKCU, Musa, HAUCK, Fabian, KLEIN, Christoph, UNAL, Ekrem, ROSENZWEIG, Sergio D., PATIROGLU, Turkan
Cyhoeddwyd 2021Text -
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CTP synthase 1 deficiency in humans reveals its central role in lymphocyte proliferation gan Martin, Emmanuel, Palmic, Noé, Sanquer, Sylvia, Lenoir, Christelle, Hauck, Fabian, Mongellaz, Cédric, Fabrega, Sylvie, Nitschké, Patrick, Esposti, Mauro Degli, Schwartzentruber, Jeremy, Taylor, Naomi, Majewski, Jacek, Jabado, Nada, Wynn, Robert, Picard, Capucine, Fischer, Alain, Arkwright, Peter, Latour, Sylvain
Cyhoeddwyd 2014Text -
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Valosin-containing protein-regulated endoplasmic reticulum stress causes NOD2-dependent inflammatory responses gan Ghalandary, Maryam, Li, Yue, Fröhlich, Thomas, Magg, Thomas, Liu, Yanshan, Rohlfs, Meino, Hollizeck, Sebastian, Conca, Raffaele, Schwerd, Tobias, Uhlig, Holm H., Bufler, Philip, Koletzko, Sibylle, Muise, Aleixo M., Snapper, Scott B., Hauck, Fabian, Klein, Christoph, Kotlarz, Daniel
Cyhoeddwyd 2022Text -
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Current Understanding and Future Research Priorities in Malignancy Associated With Inborn Errors of Immunity and DNA Repair Disorders: The Perspective of an Interdisciplinary Worki... gan 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.
Cyhoeddwyd 2018Text -
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Rubella Virus-Associated Cutaneous Granulomatous Disease: a Unique Complication in Immune-Deficient Patients, Not Limited to DNA Repair Disorders gan Buchbinder, David, Hauck, Fabian, Albert, Michael H., Rack, Anita, Bakhtiar, Shahrzad, Shcherbina, Anna, Deripapa, Elena, Sullivan, Kathleen E., Perelygina, Ludmila, Eloit, Marc, Neven, Bénédicte, Pérot, Philippe, Moshous, Despina, Suarez, Félipe, Bodemer, Christine, Bonilla, Francisco A., Vaz, Louise E., Krol, Alfons L., Klein, Christoph, Seppanen, Mikko, Nugent, Diane J., Singh, Jasjit, Ochs, Hans D.
Cyhoeddwyd 2019Text -
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NBAS Variants Are Associated with Quantitative and Qualitative NK and B Cell Deficiency gan Lenz, Dominic, Pahl, Jens, Hauck, Fabian, Alameer, Seham, Balasubramanian, Meena, Baric, Ivo, Boy, Nikolas, Church, Joseph A., Crushell, Ellen, Dick, Anke, Distelmaier, Felix, Gujar, Jidnyasa, Indolfi, Giuseppe, Lurz, Eberhard, Peters, Bianca, Schwerd, Tobias, Serranti, Daniele, Kölker, Stefan, Klein, Christoph, Hoffmann, Georg F., Prokisch, Holger, Greil, Johann, Cerwenka, Adelheid, Giese, Thomas, Staufner, Christian
Cyhoeddwyd 2021Text