Facetten
Zugriff
Einrichtung
Medientyp
- Text 12
Karte
Erscheinungsjahr
Autor/in
- Kordes, Uwe
- Schneppenheim, Reinhard
- Hasselblatt, Martin 7
- Oyen, Florian 6
- Frühwald, Michael C 5
- alle zeigen
Sprache
12 Einträge gefunden
-
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
-
-
-
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
-
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
-
-
ITI with high-dose FIX and combined immunosuppressive therapy in a patient with severe haemophilia B and inhibitor.
2009 - Forschungsinformationssystem des UKE -
-
-
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
-
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