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Autor/in
- Oyen, Florian
- Schneppenheim, Reinhard
- Obser, Tobias 13
- Frühwald, Michael C 7
- Hasselblatt, Martin 7
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33 Einträge gefunden
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Genetic and Clinical Predictors of Left Atrial Thrombus: A Single Center Case-Control Study
- Springer, Adrian
- Schleberger, Ruben
- Oyen, Florian
- Hoffmann, Boris A
- Willems, Stephan
- Meyer, Christian
- Langer, Florian
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Evidence for a low-penetrant extended phenotype of rhabdoid tumor predisposition syndrome type 1 from a kindred with gain of SMARCB1 exon 6
- Kordes, Uwe
- Mautner, Victor-Felix
- Oyen, Florian
- Hagel, Christian
- Hartmann, Christian
- Heuser, Michael
- Frühwald, Michael
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Genetic and Functional Characterization of ADAMTS13 Variants in a Patient Cohort with Upshaw-Schulman Syndrome Investigated in Germany
- Hassenpflug, Wolf Achim
- Obser, Tobias
- Bode, Julia
- Oyen, Florian
- Budde, Ulrich
- Schneppenheim, Sonja
- Schneppenheim, Reinhard
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Long-term survival of an infant with an atypical teratoid/rhabdoid tumor following subtotal resection and low-cumulative dose chemotherapy: a case report
- Arnhold, Viktor
- Oyen, Florian
- Schneppenheim, Reinhard
- Haberl, Hannes
- Koch, Arend
- Frühwald, Michael C
- Hernáiz Driever, Pablo
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Small cell undifferentiated (SCUD) hepatoblastomas: All malignant rhabdoid tumors?
- Vokuhl, Christian
- Oyen, Florian
- Häberle, Beate
- von Schweinitz, Dietrich
- Schneppenheim, Reinhard
- Leuschner, Ivo
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Molecular Analysis of Hybrid Neurofibroma/Schwannoma Identifies Common Monosomy 22 and α-T-Catenin/CTNNA3 as a Novel Candidate Tumor Suppressor
- Stahn, Verena
- Nagel, Inga
- Fischer-Huchzermeyer, Susan
- Oyen, Florian
- Schneppenheim, Reinhard
- Gesk, Stefan
- Bohring, Axel
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Detection of SMARCB1 loss in ascites cells in the diagnosis of an abdominal rhabdoid tumor
- Kerl, Kornelius
- Oyen, Florian
- Leuschner, Ivo
- Schneppenheim, Reinhard
- Nagel, Inga
- Siebert, Reiner
- Groll, Andreas H
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Characterisation of the p.A1461D mutation causing von Willebrand disease type 2B with severe thrombocytopenia, circulating giant platelets, and defective α-granule secretion
- Langer, Florian
- Obser, Tobias
- Oyen, Florian
- Spath, Brigitte
- Holstein, Katharina
- Greinacher, Andreas
- White, James G
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Platelet-free shear flow assay facilitates analysis of shear-dependent functions of VWF and ADAMTS13
- Kraus, Emma
- Kraus, Kristina
- Obser, Tobias
- Oyen, Florian
- Klemm, Ulrike
- Schneppenheim, Reinhard
- Brehm, Maria A
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High-resolution genomic analysis suggests the absence of recurrent genomic alterations other than SMARCB1 aberrations in atypical teratoid/rhabdoid tumors.
- Hasselblatt, Martin
- Isken, Sarah
- Linge, Anna
- Eikmeier, Kristin
- Jeibmann, Astrid
- Oyen, Florian
- Nagel, Inga
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Characterisation of mutations and molecular studies of type 2 von Willebrand disease.
- Ahmad, Firdos
- Jan, Rifat
- Kannan, Meganathan
- Obser, Tobias
- Hassan, Md Imtaiyaz
- Oyen, Florian
- Budde, Ulrich
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Characterisation of two novel large F8 deletions in patients with severe haemophilia A and factor VIII inhibitors.
2011 - Forschungsinformationssystem des UKE -
Nonsense mutation and inactivation of SMARCA4 (BRG1) in an atypical teratoid/rhabdoid tumor showing retained SMARCB1 (INI1) expression.
- Hasselblatt, Martin
- Gesk, Stefan
- Oyen, Florian
- Rossi, Sabrina
- Viscardi, Elisabetta
- Giangaspero, Felice
- Giannini, Caterina
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A cluster of mutations in the D3 domain of von Willebrand factor correlates with a distinct subgroup of von Willebrand disease: type 2A/IIE.
- Schneppenheim, Reinhard
- Michiels, Jan Jacques
- Obser, Tobias
- Oyen, Florian
- Pieconka, Antje
- Schneppenheim, Sonja
- Will, Kerstin