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Localised rhabdomyosarcoma in infants (<12 months) and young children (12–36 months of age) treated on the EpSSG RMS 2005 study

European journal of cancer (1990), 2022-01, Vol.160, p.206-214

2022

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Randomized Comparison of Intensified Six-Drug Versus Standard Three-Drug Chemotherapy for High-Risk Nonmetastatic Rhabdomyosarcoma and Other Chemotherapy-Sensitive Childhood Soft Tissue Sarcomas: Long-Term Results From the International Society of Pediatric Oncology MMT95 Study

Journal of clinical oncology, 2012-07, Vol.30 (20), p.2457-2465

2012

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Instability of the mitochondrial alanyl-tRNA synthetase underlies fatal infantile-onset cardiomyopathy

Human molecular genetics, 2019-01, Vol.28 (2), p.258-268

2019

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Relative frequency and morphology of cancers in carriers of germline TP53 mutations

Oncogene, 2001-08, Vol.20 (34), p.4621-4628

2001

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Biological Role and Clinical Implications of MYOD1L122R Mutation in Rhabdomyosarcoma

Cancers, 2023-03, Vol.15 (6), p.1644

2023

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FGF7–FGFR2 autocrine signaling increases growth and chemoresistance of fusion‐positive rhabdomyosarcomas

Molecular oncology, 2022-03, Vol.16 (6), p.1272-1289

2022

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Nonparameningeal head and neck rhabdomyosarcoma in children and adolescents: Lessons from the consecutive International Society of Pediatric Oncology Malignant Mesenchymal Tumor studies

Head & neck, 2017-01, Vol.39 (1), p.24-31

2017

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Pharmacological EZH2 inhibition combined with retinoic acid treatment promotes differentiation and apoptosis in rhabdomyosarcoma cells

Clinical epigenetics, 2023-10, Vol.15 (1), p.1-167, Article 167

2023

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Stratification of Wilms tumor by genetic and epigenetic analysis

Oncotarget, 2012-03, Vol.3 (3), p.327-335

2012

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The EpSSG NRSTS 2005 treatment protocol for desmoid-type fibromatosis in children: an international prospective case series

The lancet child & adolescent health, 2017-12, Vol.1 (4), p.284-292

2017

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Local staging and treatment in extremity rhabdomyosarcoma. A report from the EpSSG‐RMS2005 study

Cancer medicine (Malden, MA), 2020-10, Vol.9 (20), p.7580-7589

2020

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Genomic complexity in pediatric synovial sarcomas (Synobio study): the European pediatric soft tissue sarcoma group (EpSSG) experience

Cancer medicine (Malden, MA), 2018-04, Vol.7 (4), p.1384-1393

2018

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Relationship Between MYCN Copy Number and Expression in Rhabdomyosarcomas and Correlation With Adverse Prognosis in the Alveolar Subtype

Journal of clinical oncology, 2005-02, Vol.23 (4), p.880-888

2005

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Mesoblastic nephroma: A report of the United Kingdom children's cancer and leukaemia group (CCLG)

Pediatric blood & cancer, 2011-05, Vol.56 (5), p.744-748

2011

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Germ-line mutations of TP53 in Li-Fraumeni families : An extended study of 39 families

Cancer research (Chicago, Ill.), 1997-08, Vol.57 (15), p.3245-3252

1997

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Vinorelbine and continuous low-dose cyclophosphamide as maintenance chemotherapy in patients with high-risk rhabdomyosarcoma (RMS 2005): a multicentre, open-label, randomised, phase 3 trial

The lancet oncology, 2019-11, Vol.20 (11), p.1566-1575

2019

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Outcome After Pulmonary Radiotherapy in Wilms' Tumor Patients With Pulmonary Metastases at Diagnosis: A UK Children's Cancer Study Group, Wilms' Tumour Working Group Study

International journal of radiation oncology, biology, physics, 2008, Vol.70 (1), p.175-180

2008

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Cancer phenotype correlates with constitutional TP53 genotype in families with the Li-Fraumeni syndrome

Oncogene, 1998-09, Vol.17 (9), p.1061-1068

1998

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University students’ willingness to receive a COVID-19 vaccine in the United States

Journal of American college health, 2023-11, p.1-9

2023

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Rhabdomyosarcoma and undifferentiated round cell tumours of soft tissue in children, adolescents and young adults

Diagnostic histopathology (Oxford, England : 2008), 2023-12, Vol.29 (12), p.521-532

2023

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Spindle cell and fibrohistiocytic soft tissue tumours of infancy and childhood

Diagnostic histopathology (Oxford, England : 2008), 2023-12, Vol.29 (12), p.533-543

2023

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Central pathology review in multicenter trials and studies

Cancer, 2009-05, Vol.115 (9), p.1977-1983

2009

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Germline mutations in SUFU cause Gorlin syndrome-associated childhood medulloblastoma and redefine the risk associated with PTCH1 mutations

Journal of clinical oncology, 2014-12, Vol.32 (36), p.4155-4161

2014

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Genomic Classification and Clinical Outcome in Rhabdomyosarcoma: A Report From an International Consortium

Journal of clinical oncology, 2021-09, Vol.39 (26), p.2859-2871

2021

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Localised rhabdomyosarcoma in infants (<12 months) and young children (12–36 months of age) treated on the EpSSG RMS 2005 study

Randomized Comparison of Intensified Six-Drug Versus Standard Three-Drug Chemotherapy for High-Risk Nonmetastatic Rhabdomyosarcoma and Other Chemotherapy-Sensitive Childhood Soft Tissue Sarcomas: Long-Term Results From the International Society of Pediatric Oncology MMT95 Study

Instability of the mitochondrial alanyl-tRNA synthetase underlies fatal infantile-onset cardiomyopathy

Relative frequency and morphology of cancers in carriers of germline TP53 mutations

Biological Role and Clinical Implications of MYOD1L122R Mutation in Rhabdomyosarcoma

FGF7–FGFR2 autocrine signaling increases growth and chemoresistance of fusion‐positive rhabdomyosarcomas

Nonparameningeal head and neck rhabdomyosarcoma in children and adolescents: Lessons from the consecutive International Society of Pediatric Oncology Malignant Mesenchymal Tumor studies

Frontline and Relapsed Rhabdomyosarcoma (FAR-RMS) Clinical Trial: A Report from the European Paediatric Soft Tissue Sarcoma Study Group (EpSSG)

Pharmacological EZH2 inhibition combined with retinoic acid treatment promotes differentiation and apoptosis in rhabdomyosarcoma cells

Stratification of Wilms tumor by genetic and epigenetic analysis

The EpSSG NRSTS 2005 treatment protocol for desmoid-type fibromatosis in children: an international prospective case series

Local staging and treatment in extremity rhabdomyosarcoma. A report from the EpSSG‐RMS2005 study

Genomic complexity in pediatric synovial sarcomas (Synobio study): the European pediatric soft tissue sarcoma group (EpSSG) experience

Relationship Between MYCN Copy Number and Expression in Rhabdomyosarcomas and Correlation With Adverse Prognosis in the Alveolar Subtype

Mesoblastic nephroma: A report of the United Kingdom children's cancer and leukaemia group (CCLG)

Germ-line mutations of TP53 in Li-Fraumeni families : An extended study of 39 families

Vinorelbine and continuous low-dose cyclophosphamide as maintenance chemotherapy in patients with high-risk rhabdomyosarcoma (RMS 2005): a multicentre, open-label, randomised, phase 3 trial

Outcome After Pulmonary Radiotherapy in Wilms' Tumor Patients With Pulmonary Metastases at Diagnosis: A UK Children's Cancer Study Group, Wilms' Tumour Working Group Study

Cancer phenotype correlates with constitutional TP53 genotype in families with the Li-Fraumeni syndrome

University students’ willingness to receive a COVID-19 vaccine in the United States

Rhabdomyosarcoma and undifferentiated round cell tumours of soft tissue in children, adolescents and young adults

Spindle cell and fibrohistiocytic soft tissue tumours of infancy and childhood

Central pathology review in multicenter trials and studies

Germline mutations in SUFU cause Gorlin syndrome-associated childhood medulloblastoma and redefine the risk associated with PTCH1 mutations

Genomic Classification and Clinical Outcome in Rhabdomyosarcoma: A Report From an International Consortium

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