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2. Intraoperative Immuntherapie mit dem trifunktionalen Antikörper Catumaxomab bei Patienten mit fortgeschrittenem Magen-, Colon- und Pankreaskarzinom: Ergebnisse einer Phase I Pilotstudie

3. Rhabdoid 2007 and EU-RHAB - results of two European registries with consensus treatment recommendations for 139 children with rhabdoid tumors

4. Genetic alterations of SMARCA4 in atypical teratoid/rhabdoid tumours (AT/RT) are associated with higher frequency of germ line alterations and shorter survival as compared to SMARCB1 deficient AT/RT

12. EU-RHAB: Ergebnisse des europäischen Verbundprojektes zur Erfassung und Behandlung von Kindern mit Rhabdoiden Tumoren

13. Clinical Characteristics and Outcome of Children with Extracranial, Extrarenal Rhabdoid Tumors Registered to the European Rhabdoid Registry 2007–2013

14. ATYPICAL TERATOID RHABDOID TUMOUR

15. Feasibility of Intensive Multimodal Therapy in Infants Affected by Rhabdoid Tumors – Experience of the EU-RHAB registry

17. ATYPICAL TERATOID RHABDOID TUMOR (ATRT)

20. Treatment of peritoneal carcinomatosis due to GI-tract cancer by intraperitoneal application of the trifunctional antibody catumaxomab (anti-EpcAM x anti-CD3): Results of a phase I/II trial

23. Improved 6-year overall survival in AT/RT - results of the registry study Rhabdoid 2007.

24. Detection of SMARCB1 loss in ascites cells in the diagnosis of an abdominal rhabdoid tumor.

25. Synchronous congenital malignant rhabdoid tumor of the orbit and atypical teratoid/rhabdoid tumor--feasibility and efficacy of multimodal therapy in a long-term survivor.

26. Clinical and genetic features of rhabdoid tumors of the heart registered with the European Rhabdoid Registry (EU-RHAB).

27. SMARCA4-mutated atypical teratoid/rhabdoid tumors are associated with inherited germline alterations and poor prognosis.

28. Arsenic trioxide inhibits tumor cell growth in malignant rhabdoid tumors in vitro and in vivo by targeting overexpressed Gli1.

29. Identification of genes involved in the biology of atypical teratoid/rhabdoid tumours using Drosophila melanogaster.

30. Favorable outcome of patients affected by rhabdoid tumors due to rhabdoid tumor predisposition syndrome (RTPS).

31. High-resolution genomic analysis suggests the absence of recurrent genomic alterations other than SMARCB1 aberrations in atypical teratoid/rhabdoid tumors.

32. Nine months to progression using fourth-line liposomally encapsulated paclitaxel against hepatocellular carcinoma.

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