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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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Pancytopenia in a 4-year-old boy. 22q11.2 microdeletion syndrome.
2009 - Forschungsinformationssystem des UKE -
The problem of novel FVIII missense mutations for haemophilia A genetic counseling.
2009 - Forschungsinformationssystem des UKE -
Variations in the ratio between von Willebrand factor and its cleaving protease during systemic inflammation and association with severity and prognosis of organ failure.
- Claus, Ralf A
- Bockmeyer, Clemens L
- Ulrich, Budde
- Kentouche, Karim
- Sossdorf, Maik
- Hilberg, Thomas
- Schneppenheim, Reinhard
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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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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 -
An Alu-mediated novel large deletion is the most frequent cause of type 3 von Willebrand disease in Hungary.
2008 - Forschungsinformationssystem des UKE -
Inflammation-associated ADAMTS13 deficiency promotes formation of ultra-large von Willebrand factor.
- Bockmeyer, Clemens L
- Claus, Ralf A
- Budde, Ulrich
- Kentouche, Karim
- Schneppenheim, Reinhard
- Lösche, Wolfgang
- Reinhart, Konrad
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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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Genetic defects in von Willebrand disease type 3 in Indian and Greek patients.
2008 - Forschungsinformationssystem des UKE -
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Mutation spectrum in children with primary hemophagocytic lymphohistiocytosis: molecular and functional analyses of PRF1, UNC13D, STX11, and RAB27A.
- Zur Stadt, Udo
- Beutel, Karin
- Kolberg, Susanne
- Schneppenheim, Reinhard
- Kabisch, Hartmut
- Janka, Gritta
- Hennies, Hans Christian
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Non-linkage of familial rhabdoid tumors to SMARCB1 implies a second locus for the rhabdoid tumor predisposition syndrome.
- Frühwald, Michael C
- Hasselblatt, Martin
- Wirth, Sebastian
- Köhler, Gabriele
- Schneppenheim, Reinhard
- Subero, Jose Igancio Martin
- Siebert, Reiner
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Intracranial hemorrhage in a term newborn with severe von Willebrand disease type 3 associated with sinus venous thrombosis.
- Wetzstein, Viola
- Ulrich, Budde
- Oyen, Florian
- Ding, Xiaoqi
- Herrmann, Jochen
- Liebig, Birte
- Schneppenheim, Reinhard
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A common origin of the 4143insA ADAMTS13 mutation.
- Schneppenheim, Reinhard
- Hovinga, Kremer
- Johanna, A
- Becker, Tim
- Ulrich, Budde
- Karpman, Diana
- Brockhaus, Wolfgang