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Autor/in
- Beutel, Karin
- Janka-Schaub, Gritta 7
- Lehmberg, Kai 6
- Schneppenheim, Reinhard 6
- Zur Stadt, Udo 6
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34 Einträge gefunden
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Consensus-Based Guidelines for the Recognition, Diagnosis, and Management of Hemophagocytic Lymphohistiocytosis in Critically Ill Children and Adults
- Hines, Melissa R
- von Bahr Greenwood, Tatiana
- Beutel, Gernot
- Beutel, Karin
- Hays, J Allyson
- Horne, AnnaCarin
- Janka, Gritta
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Malignancy-associated haemophagocytic lymphohistiocytosis in children and adolescents
- Lehmberg, Kai
- Sprekels, Björn
- Nichols, Kim E
- Woessmann, Wilhelm
- Müller, Ingo
- Suttorp, Meinolf
- Bernig, Toralf
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Treosulfan-based conditioning regimen for children and adolescents with hemophagocytic lymphohistiocytosis
- Lehmberg, Kai
- Albert, Michael H
- Beier, Rita
- Beutel, Karin
- Gruhn, Bernd
- Kröger, Nicolaus-Martin
- Meisel, Roland
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Distinct mutations in STXBP2 are associated with variable clinical presentations in patients with familial hemophagocytic lymphohistiocytosis type 5 (FHL5)
- Pagel, Julia
- Beutel, Karin
- Lehmberg, Kai
- Koch, Florian
- Maul-Pavicic, Andrea
- Rohlfs, Anna-Katharina
- Al-Jefri, Abdullah
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Risk factors for early death in children with haemophagocytic lymphohistiocytosis.
- Trottestam, Helena
- Berglöf, Elisabet
- Horne, AnnaCarin
- Onelöv, Erik
- Beutel, Karin
- Lehmberg, Kai
- Sieni, Elena
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Genotype-phenotype study of familial haemophagocytic lymphohistiocytosis type 3.
- Sieni, Elena
- Cetica, Valentina
- Santoro, Alessandra
- Beutel, Karin
- Mastrodicasa, Elena
- Meeths, Marie
- Ciambotti, Benedetta
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STXBP2 mutations in children with familial haemophagocytic lymphohistiocytosis type 5.
- Cetica, Valentina
- Santoro, Alessandra
- Gilmour, Kimberly C
- Sieni, Elena
- Beutel, Karin
- Pende, Daniela
- Marcenaro, Stefania
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Atypical familial hemophagocytic lymphohistiocytosis due to mutations in UNC13D and STXBP2 overlaps with primary immunodeficiency diseases
- Rohr, Jan
- Beutel, Karin
- Maul-Pavicic, Andrea
- Vraetz, Thomas
- Thiel, Jens
- Warnatz, Klaus
- Bondzio, Ilka
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ITI with high-dose FIX and combined immunosuppressive therapy in a patient with severe haemophilia B and inhibitor.
2009 - Forschungsinformationssystem des UKE -
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Clinical presentation of Griscelli syndrome type 2 and spectrum of RAB27A mutations.
- Meeths, Marie
- Bryceson, Yenan T
- Rudd, Eva
- Zheng, Chengyun
- Wood, Stephanie M
- Ramme, Kim
- Beutel, Karin
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Response to DDAVP in children with von Willebrand disease type 2.
- Schneppenheim, Reinhard
- Budde, U
- Beutel, Karin
- Hassenpflug, W-A
- Hauch, H
- Obser, Tobias
- Oyen, Florian
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Molecular analysis and clinical aspects of four patients with Chédiak-Higashi syndrome (CHS).
2009 - Forschungsinformationssystem des UKE -
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Successful donor-lymphocyte infusion for extreme immune-hemolysis following unrelated BMT in a patient with X-linked chronic granulomatous disease and McLeod phenotype.
- Kordes, Uwe
- Binder, Thomas
- Eiermann, Thomas
- Hassenpflug-Diedrich, B
- Hassan, M A
- Beutel, Karin
- Nagy, M