6 Einträge gefunden

1. Rapid Diagnosis of an AT/RT by the Detection of a Heterozygous SMARCB1 Germ Line Deletion in an Infant

   1. Kerl, Kornelius
   2. Oyen, Florian
   3. Giannikopoulou, Dimitra
   4. Rössig, Claudia
   5. Rellensmann, Georg
   6. Sandkötter, Julia
   7. Brentrup, Angela

   2016 - Forschungsinformationssystem des UKE
2. Poorly differentiated chordoma with SMARCB1/INI1 loss: a distinct molecular entity with dismal prognosis

   1. Hasselblatt, Martin
   2. Thomas, Christian
   3. Hovestadt, Volker
   4. Schrimpf, Daniel
   5. Johann, Pascal
   6. Bens, Susanne
   7. Oyen, Florian

   2016 - Forschungsinformationssystem des UKE
3. The Prevalence of Sickle Cell Disease and Its Implication for Newborn Screening in Germany (Hamburg Metropolitan Area)

   1. Grosse, Regine
   2. Lukacs, Zoltan
   3. Cobos, Paulina Nieves
   4. Oyen, Florian
   5. Ehmen, Christa
   6. Muntau, Birgit
   7. Timmann, Christian

   2016 - Forschungsinformationssystem des UKE
4. Long-term survival of an infant with an atypical teratoid/rhabdoid tumor following subtotal resection and low-cumulative dose chemotherapy: a case report

   1. Arnhold, Viktor
   2. Oyen, Florian
   3. Schneppenheim, Reinhard
   4. Haberl, Hannes
   5. Koch, Arend
   6. Frühwald, Michael C
   7. Hernáiz Driever, Pablo

   2016 - Forschungsinformationssystem des UKE
5. Small cell undifferentiated (SCUD) hepatoblastomas: All malignant rhabdoid tumors?

   1. Vokuhl, Christian
   2. Oyen, Florian
   3. Häberle, Beate
   4. von Schweinitz, Dietrich
   5. Schneppenheim, Reinhard
   6. Leuschner, Ivo

   2016 - Forschungsinformationssystem des UKE
6. Molecular Analysis of Hybrid Neurofibroma/Schwannoma Identifies Common Monosomy 22 and α-T-Catenin/CTNNA3 as a Novel Candidate Tumor Suppressor

   1. Stahn, Verena
   2. Nagel, Inga
   3. Fischer-Huchzermeyer, Susan
   4. Oyen, Florian
   5. Schneppenheim, Reinhard
   6. Gesk, Stefan
   7. Bohring, Axel

   2016 - Forschungsinformationssystem des UKE