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Autor/in
- Beutel, Karin
- Janka-Schaub, Gritta 5
- Schneppenheim, Reinhard 5
- Simon, A 4
- Kabisch, Hartmut 3
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22 Einträge gefunden
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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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ITI with high-dose FIX and combined immunosuppressive therapy in a patient with severe haemophilia B and inhibitor.
2009 - Forschungsinformationssystem des UKE -
Molecular analysis and clinical aspects of four patients with Chédiak-Higashi syndrome (CHS).
2009 - Forschungsinformationssystem des UKE -
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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Genotype-phenotype study of familial haemophagocytic lymphohistiocytosis due to perforin mutations.
2008 - 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
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Pneumococcal conjugate vaccine provides early protective antibody responses in children after related and unrelated allogeneic hematopoietic stem cell transplantation.
- Meisel, Roland
- Kuypers, Lisa
- Dirksen, Uta
- Schubert, Ralf
- Gruhn, Bernd
- Strauss, Gabriele
- Beutel, Karin
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[Viral infections in pediatric cancer patients]
2005 - Forschungsinformationssystem des UKE -
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A91V is a polymorphism in the perforin gene not causative of an FHLH phenotype.
- Udo, Zur Stadt
- Beutel, Karin
- Weber, Belinda
- Kabisch, Hartmut
- Schneppenheim, Reinhard
- Janka-Schaub, Gritta