Facetten
Zugriff
Einrichtung
Medientyp
- Text 42
Karte
Erscheinungsjahr
Autor/in
- Schneppenheim, Reinhard
- Oyen, Florian 11
- Budde, U 10
- Obser, Tobias 9
- Ulrich, Budde 9
- alle zeigen
Sprache
42 Einträge gefunden
-
Unterarmgangrän bei "normaler" Gerinnung.
- Blohm, Martin
- Lehmberg, Kai
- Schrum, Johanna
- Helmke, Knut
- Ridderbusch, Ina
- Schneppenheim, Reinhard
- Singer, Dominique
-
-
Difficulties in diagnosing congenital thrombotic thrombocytopenic purpura.
2010 - Forschungsinformationssystem des UKE -
Neonatal cholestasis and glucose-6-P-dehydrogenase deficiency.
- Kordes, Uwe
- Briem-Richter, Andrea
- Santer, René
- Schäfer, Hansjörg
- Singer, Dominique
- Sonntag, Josef
- Steuerwald, Ulrike
-
-
Neonatal cholestasis in glucose-6-phosphate dehydrogenase deficiency.
- Kordes, Uwe
- Briem-Richter, Andrea
- Santer, René
- Schäfer, Hansjörg
- Singer, Dominique
- Sonntag, J
- Steuerwald, U
-
-
-
Homozygous type 2N R854W von Willebrand factor is poorly secreted and causes a severe von Willebrand disease phenotype.
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
-
-
-
-
ITI with high-dose FIX and combined immunosuppressive therapy in a patient with severe haemophilia B and inhibitor.
2009 - Forschungsinformationssystem des UKE -
-
-
Shear-induced unfolding activates von Willebrand factor A2 domain for proteolysis.
2009 - Forschungsinformationssystem des UKE -
Pancytopenia in a 4-year-old boy. 22q11.2 microdeletion syndrome.
2009 - Forschungsinformationssystem des UKE -
-
Heterozygous missense protein S mutation in a young boy with incomplete tetraplegia.
2009 - Forschungsinformationssystem des UKE