5 Einträge gefunden

1. Evidence for a low-penetrant extended phenotype of rhabdoid tumor predisposition syndrome type 1 from a kindred with gain of SMARCB1 exon 6

   1. Kordes, Uwe
   2. Mautner, Victor-Felix
   3. Oyen, Florian
   4. Hagel, Christian
   5. Hartmann, Christian
   6. Heuser, Michael
   7. Frühwald, Michael

   2021 - Forschungsinformationssystem des UKE
2. Germline variants in SMARCB1 and other members of the BAF chromatin-remodeling complex across human disease entities:a meta-analysis

   1. Holsten, Till
   2. Bens, Susanne
   3. Oyen, Florian
   4. Nemes, Karolina
   5. Hasselblatt, Martin
   6. Kordes, Uwe
   7. Siebert, Reiner

   2018 - Forschungsinformationssystem des UKE
3. Favorable outcome of patients affected by rhabdoid tumors due to rhabdoid tumor predisposition syndrome (RTPS)

   1. Kordes, Uwe
   2. Bartelheim, Kerstin
   3. Modena, Piergiorgio
   4. Massimino, Maura
   5. Biassoni, Veronica
   6. Reinhard, Harald
   7. Hasselblatt, Martin

   2014 - Forschungsinformationssystem des UKE
4. High-resolution genomic analysis suggests the absence of recurrent genomic alterations other than SMARCB1 aberrations in atypical teratoid/rhabdoid tumors.

   1. Hasselblatt, Martin
   2. Isken, Sarah
   3. Linge, Anna
   4. Eikmeier, Kristin
   5. Jeibmann, Astrid
   6. Oyen, Florian
   7. Nagel, Inga

   2013 - Forschungsinformationssystem des UKE
5. Cribriform neuroepithelial tumor (CRINET): a nonrhabdoid ventricular tumor with INI1 loss and relatively favorable prognosis.

   1. Hasselblatt, Martin
   2. Oyen, Florian
   3. Gesk, Stefan
   4. Kordes, Uwe
   5. Brigitte, Wrede
   6. Bergmann, Markus
   7. Schmid, Hansjörg

   2009 - Forschungsinformationssystem des UKE