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Survey of Paediatric Oncologists and Pathologists regarding Their Views and Experiences with Variant Translocations in Ewing and Ewing-Like Sarcoma: A Report of the Children’s Oncology Group

Complexity (New York, N.Y.), 2020, Vol.2020 (2020), p.1-9

2020

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Axillary Lymph Node Dissection in Angiosarcomas of the Breast: An Asian Institutional Perspective

Complexity (New York, N.Y.), 2020, Vol.2020 (2020), p.1-5

2020

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Aktuelle Überlegungen zur System- und Lokaltherapie beim Ewing-Sarkom

Die Onkologie, 2022-07, Vol.28 (7), p.563-571

2022

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Comparison of Epidemiology, Clinical Features, and Outcomes of Patients with Reported Ewing Sarcoma and PNET over 40 Years Justifies Current WHO Classification and Treatment Approaches

Complexity (New York, N.Y.), 2018, Vol.2018 (2018), p.1-6

2018

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Cell-to-cell heterogeneity of EWSR1-FLI1 activity determines proliferation/migration choices in Ewing sarcoma cells

Oncogene, 2017-06, Vol.36 (25), p.3505-3514

2017

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Knochensarkom des Kindes-, Jugend- und jungen Erwachsenenalters

Der Onkologe, 2013-08, Vol.19 (8), p.657-666

Dirksen, U.

2013

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Exploring long-term cancer survivors' care experiences and unmet needs: protocol for a qualitative study

BMC cancer, 2024-07, Vol.24 (1), p.783-5, Article 783

2024

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Das Ewing-Sarkom

TumorDiagnostik & Therapie, 2010-08, Vol.31 (4), p.202-204

Dirksen, U

2010

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Prevalence of the Hippo Effectors YAP1/TAZ in Tumors of Soft Tissue and Bone

Scientific reports, 2019-12, Vol.9 (1), p.19704-9, Article 19704

2019

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The CXCR4 antagonist Plerixafor (AMD3100) promotes Ewing sarcoma cell survival and migration in Ewing sarcoma cells in vitro

European journal of cancer (1990), 2016-12, Vol.69, p.S50-S50

2016

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Individual risk evaluation for local recurrence and distant metastasis in Ewing sarcoma: A multistate model: A multistate model for Ewing sarcoma

Pediatric blood & cancer, 2019-11, Vol.66 (11), p.e27943-e27943

2019

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Identification of novel therapeutic targets in Ewing sarcoma using a pooled shRNA screening approach in a tumor cell-specific environment

European journal of cancer (1990), 2016-12, Vol.69, p.S50-S50

2016

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Correction to: No difference in survival after HLA mismatched versus HLA matched allogeneic stem cell transplantation in Ewing sarcoma patients with advanced disease

Bone marrow transplantation (Basingstoke), 2021-09, Vol.56 (9), p.2320-2320

2021

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1q gain and CDT2 overexpression underlie an aggressive and highly proliferative form of Ewing sarcoma

Oncogene, 2012-03, Vol.31 (10), p.1287-1298

2012

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Management of Bone Tumours in Paediatric Oncology

Clinical oncology (Royal College of Radiologists (Great Britain)), 2013-01, Vol.25 (1), p.19-26

2013

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Effective childhood cancer treatment: The impact of large scale clinical trials in Germany and Austria

Pediatric blood & cancer, 2013-10, Vol.60 (10), p.1574-1581

2013

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Individual risk evaluation for local recurrence and distant metastasis in Ewing sarcoma: A multistate model

Pediatric blood & cancer, 2019-11, Vol.66 (11), p.n/a

2019

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Trabectedin Followed by Irinotecan Can Stabilize Disease in Advanced Translocation-Positive Sarcomas with Acceptable Toxicity

Complexity (New York, N.Y.), 2016, Vol.2016 (2016), p.218-223

2016

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3407 Identification of novel EWS-FLI1 specific targets in Ewing sarcoma through pooled shRNA screens

European journal of cancer (1990), 2015-09, Vol.51, p.S691-S691

2015

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3450 The receptor tyrosine kinase RON: a challenging therapeutic target in Ewing sarcoma metastases

European journal of cancer (1990), 2015-09, Vol.51, p.S705-S705

2015

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3406 Receptor tyrosine kinase gene expression analyses of Ewing sarcomas identify ROR1 as a potential therapeutic target in metastatic disease

European journal of cancer (1990), 2015-09, Vol.51, p.S690-S690

2015

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Investigating the heterogeneity of alkylating agents’ efficacy and toxicity between sexes: A systematic review and meta‐analysis of randomized trials comparing cyclophosphamide and ifosfamide (MAIAGE study)

Pediatric blood & cancer, 2017-08, Vol.64 (8), p.n/a

2017

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Single-Centre Experience of Systemic Treatment with Vincristine, Ifosfamide, and Doxorubicin Alternating with Etoposide, Ifosfamide, and Cisplatin in Adult Patients with Ewing Sarcoma

Complexity (New York, N.Y.), 2017, Vol.2017 (2017), p.1-7-002

2017

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420 Analysis of genomic alterations in Ewing sarcoma (German cohort) reveals cooperating mutations and novel therapy targets

European journal of cancer (1990), 2014-11, Vol.50, p.134-134

2014

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Survey of Paediatric Oncologists and Pathologists regarding Their Views and Experiences with Variant Translocations in Ewing and Ewing-Like Sarcoma: A Report of the Children’s Oncology Group

Axillary Lymph Node Dissection in Angiosarcomas of the Breast: An Asian Institutional Perspective

Aktuelle Überlegungen zur System- und Lokaltherapie beim Ewing-Sarkom

Comparison of Epidemiology, Clinical Features, and Outcomes of Patients with Reported Ewing Sarcoma and PNET over 40 Years Justifies Current WHO Classification and Treatment Approaches

Cell-to-cell heterogeneity of EWSR1-FLI1 activity determines proliferation/migration choices in Ewing sarcoma cells

Knochensarkom des Kindes-, Jugend- und jungen Erwachsenenalters

Exploring long-term cancer survivors' care experiences and unmet needs: protocol for a qualitative study

Das Ewing-Sarkom

Prevalence of the Hippo Effectors YAP1/TAZ in Tumors of Soft Tissue and Bone

The CXCR4 antagonist Plerixafor (AMD3100) promotes Ewing sarcoma cell survival and migration in Ewing sarcoma cells in vitro

Individual risk evaluation for local recurrence and distant metastasis in Ewing sarcoma: A multistate model: A multistate model for Ewing sarcoma

Identification of novel therapeutic targets in Ewing sarcoma using a pooled shRNA screening approach in a tumor cell-specific environment

Correction to: No difference in survival after HLA mismatched versus HLA matched allogeneic stem cell transplantation in Ewing sarcoma patients with advanced disease

Comprehensive assessments and related interventions to enhance the long-term outcomes of child, adolescent and young adult cancer survivors - presentation of the CARE for CAYA-Program study protocol and associated literature review

1q gain and CDT2 overexpression underlie an aggressive and highly proliferative form of Ewing sarcoma

Management of Bone Tumours in Paediatric Oncology

Effective childhood cancer treatment: The impact of large scale clinical trials in Germany and Austria

Individual risk evaluation for local recurrence and distant metastasis in Ewing sarcoma: A multistate model

Trabectedin Followed by Irinotecan Can Stabilize Disease in Advanced Translocation-Positive Sarcomas with Acceptable Toxicity

3407 Identification of novel EWS-FLI1 specific targets in Ewing sarcoma through pooled shRNA screens

3450 The receptor tyrosine kinase RON: a challenging therapeutic target in Ewing sarcoma metastases

3406 Receptor tyrosine kinase gene expression analyses of Ewing sarcomas identify ROR1 as a potential therapeutic target in metastatic disease

Investigating the heterogeneity of alkylating agents’ efficacy and toxicity between sexes: A systematic review and meta‐analysis of randomized trials comparing cyclophosphamide and ifosfamide (MAIAGE study)

Single-Centre Experience of Systemic Treatment with Vincristine, Ifosfamide, and Doxorubicin Alternating with Etoposide, Ifosfamide, and Cisplatin in Adult Patients with Ewing Sarcoma

420 Analysis of genomic alterations in Ewing sarcoma (German cohort) reveals cooperating mutations and novel therapy targets

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