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Discrete‐choice experiment to analyse preferences for centralizing specialist cancer surgery services

British journal of surgery, 2018-04, Vol.105 (5), p.587-596

2018

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Congenital mesoblastic nephroma 50 years after its recognition: A narrative review

Pediatric blood & cancer, 2017-07, Vol.64 (7), p.n/a

2017

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Prognostic significance of age in 5631 patients with Wilms tumour prospectively registered in International Society of Paediatric Oncology (SIOP) 93-01 and 2001

PloS one, 2019-08, Vol.14 (8), p.e0221373

2019

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Population survival from childhood cancer in Britain during 1978–2005 by eras of entry to clinical trials

Annals of oncology, 2012-09, Vol.23 (9), p.2464-2469

2012

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Fifty years of clinical and research studies for childhood renal tumors within the International Society of Pediatric Oncology (SIOP)

Annals of oncology, 2021-11, Vol.32 (11), p.1327-1331

2021

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Activation of the hedgehog pathway confers a poor prognosis in embryonal and fusion gene-negative alveolar rhabdomyosarcoma

Oncogene, 2010-12, Vol.29 (48), p.6323-6330

2010

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The European study on centralisation of childhood cancer treatment

European journal of cancer (1990), 2019-07, Vol.115, p.120-127

2019

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Gain of 1q is a marker of poor prognosis in Wilms' tumors

Genes chromosomes & cancer, 2013-11, Vol.52 (11), p.1065-1074

2013

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Incidence and outcomes of patients with late recurrence of Wilms' tumor

Pediatric blood & cancer, 2013-10, Vol.60 (10), p.1612-1615

2013

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Treatment of relapsed Wilms tumour (WT) patients: Experience with topotecan. A report from the SIOP Renal Tumour Study Group (RTSG)

Pediatric blood & cancer, 2015-04, Vol.62 (4), p.598-602

2015

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Evidence-based data and rare cancers: The need for a new methodological approach in research and investigation

European journal of surgical oncology, 2019-01, Vol.45 (1), p.22-30

2019

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Surveillance for Wilms tumour in at-risk children: pragmatic recommendations for best practice

Archives of disease in childhood, 2006-12, Vol.91 (12), p.995-999

2006

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Array CGH profiling of favourable histology Wilms tumours reveals novel gains and losses associated with relapse

The Journal of pathology, 2006-09, Vol.210 (1), p.49-58

2006

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Clinical trials for children with cancer in Europe – Still a long way from harmonisation: A report from SIOP Europe

European journal of cancer (1990), 2008-10, Vol.44 (15), p.2106-2111

Pritchard-Jones, K

2008

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PAX7 expression in embryonal rhabdomyosarcoma suggests an origin in muscle satellite cells

British journal of cancer, 2003-07, Vol.89 (2), p.327-332

2003

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Older Age Is an Adverse Prognostic Factor in Stage I, Favorable Histology Wilms’ Tumor Treated With Vincristine Monochemotherapy: A Study by the United Kingdom Children’s Cancer Study Group, Wilm’s Tumor Working Group

Journal of clinical oncology, 2003-09, Vol.21 (17), p.3269-3275

2003

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Analysis by array CGH of genomic changes associated with the progression or relapse of Wilms' tumour

The Journal of pathology, 2007-01, Vol.211 (1), p.52-59

2007

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Treatment and outcome of Wilms' tumour patients: an analysis of all cases registered in the UKW3 trial

Annals of oncology, 2012-09, Vol.23 (9), p.2457-2463

2012

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Risk factors for local recurrence in Wilms tumour and the potential influence of biopsy – The United Kingdom experience

European journal of cancer (1990), 2015-01, Vol.51 (2), p.225-232

2015

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MicroRNA-206 expression levels correlate with clinical behaviour of rhabdomyosarcomas

British journal of cancer, 2010-06, Vol.102 (12), p.1769-1777

2010

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Outcome of localised blastemal-type Wilms tumour patients treated according to intensified treatment in the SIOP WT 2001 protocol, a report of the SIOP Renal Tumour Study Group (SIOP-RTSG)

European journal of cancer (1990), 2015-03, Vol.51 (4), p.498-506

2015

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Treatment and outcome of patients with relapsed clear cell sarcoma of the kidney: a combined SIOP and AIEOP study

British journal of cancer, 2014-07, Vol.111 (2), p.227-233

2014

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172 INVITED ‘Spread of Excellence’ (Dissemination) Activities of the European Network of Excellence for Cancer Research in Children and Adolescents (ENCCA)

European journal of cancer (1990), 2011, Vol.47, p.S41-S42

Pritchard-Jones, K

2011

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Controversies and advances in the management of Wilms’ tumour

Archives of Disease in Childhood, 2002-09, Vol.87 (3), p.241-244

Pritchard-Jones, K

2002

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A prospective study of admissions for febrile neutropenia in secondary paediatric units in South East England

Pediatric Blood & Cancer, 2007-10, Vol.49 (5), p.678-681

2007

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Discrete‐choice experiment to analyse preferences for centralizing specialist cancer surgery services

Congenital mesoblastic nephroma 50 years after its recognition: A narrative review

Prognostic significance of age in 5631 patients with Wilms tumour prospectively registered in International Society of Paediatric Oncology (SIOP) 93-01 and 2001

Population survival from childhood cancer in Britain during 1978–2005 by eras of entry to clinical trials

Fifty years of clinical and research studies for childhood renal tumors within the International Society of Pediatric Oncology (SIOP)

Activation of the hedgehog pathway confers a poor prognosis in embryonal and fusion gene-negative alveolar rhabdomyosarcoma

The European study on centralisation of childhood cancer treatment

Gain of 1q is a marker of poor prognosis in Wilms' tumors

Incidence and outcomes of patients with late recurrence of Wilms' tumor

Treatment of relapsed Wilms tumour (WT) patients: Experience with topotecan. A report from the SIOP Renal Tumour Study Group (RTSG)

Evidence-based data and rare cancers: The need for a new methodological approach in research and investigation

Surveillance for Wilms tumour in at-risk children: pragmatic recommendations for best practice

Array CGH profiling of favourable histology Wilms tumours reveals novel gains and losses associated with relapse

Clinical trials for children with cancer in Europe – Still a long way from harmonisation: A report from SIOP Europe

PAX7 expression in embryonal rhabdomyosarcoma suggests an origin in muscle satellite cells

Older Age Is an Adverse Prognostic Factor in Stage I, Favorable Histology Wilms’ Tumor Treated With Vincristine Monochemotherapy: A Study by the United Kingdom Children’s Cancer Study Group, Wilm’s Tumor Working Group

Analysis by array CGH of genomic changes associated with the progression or relapse of Wilms' tumour

Treatment and outcome of Wilms' tumour patients: an analysis of all cases registered in the UKW3 trial

Risk factors for local recurrence in Wilms tumour and the potential influence of biopsy – The United Kingdom experience

MicroRNA-206 expression levels correlate with clinical behaviour of rhabdomyosarcomas

Outcome of localised blastemal-type Wilms tumour patients treated according to intensified treatment in the SIOP WT 2001 protocol, a report of the SIOP Renal Tumour Study Group (SIOP-RTSG)

Treatment and outcome of patients with relapsed clear cell sarcoma of the kidney: a combined SIOP and AIEOP study

172 INVITED ‘Spread of Excellence’ (Dissemination) Activities of the European Network of Excellence for Cancer Research in Children and Adolescents (ENCCA)

Controversies and advances in the management of Wilms’ tumour

A prospective study of admissions for febrile neutropenia in secondary paediatric units in South East England

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