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Autor/in
- Schneppenheim, Reinhard
- Obser, Tobias 38
- Oyen, Florian 33
- Budde, Ulrich 20
- Budde, U 13
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110 Einträge gefunden
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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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Difficulties in diagnosing congenital thrombotic thrombocytopenic purpura.
2010 - Forschungsinformationssystem des UKE -
Loss of SMARCB1/INI1 expression in poorly differentiated chordomas.
- Mobley, Bret C
- McKenney, Jesse K
- Bangs, Charles D
- Callahan, Katherine
- Yeom, Kristen W
- Schneppenheim, Reinhard
- Hayden, Melanie G
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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
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Neonatal cholestasis and glucose-6-P-dehydrogenase deficiency.
- Kordes, Uwe
- Briem-Richter, Andrea
- Santer, René
- Schäfer, Hansjörg
- Singer, Dominique
- Sonntag, Josef
- Steuerwald, Ulrike
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Neonatal cholestasis in glucose-6-phosphate dehydrogenase deficiency.
- Kordes, Uwe
- Briem-Richter, Andrea
- Santer, René
- Schäfer, Hansjörg
- Singer, Dominique
- Sonntag, J
- Steuerwald, U
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Homozygous type 2N R854W von Willebrand factor is poorly secreted and causes a severe von Willebrand disease phenotype.
2010 - Forschungsinformationssystem des UKE -
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Acquired von Willebrand syndrome as side effect of valproic acid therapy in children is rare.
2009 - Forschungsinformationssystem des UKE -
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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