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Bilateral Wilms tumour: a review of clinical and molecular features

Bilateral Wilms tumour: a review of clinical and molecular features

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_5687181

Bilateral Wilms tumour: a review of clinical and molecular features

About this item

Full title

Bilateral Wilms tumour: a review of clinical and molecular features

Publisher

Cambridge, UK: Cambridge University Press

Journal title

Expert reviews in molecular medicine, 2017-07, Vol.19, p.e8-e8, Article e8

Language

English

Formats

Publication information

Publisher

Cambridge, UK: Cambridge University Press

More information

Scope and Contents

Contents

Wilms tumour (WT) is the most common paediatric kidney cancer and affects approximately one in 10 000 children. The tumour is associated with undifferentiated embryonic lesions called nephrogenic rests (NRs) or, when diffuse, nephroblastomatosis. WT or NRs can occur in both kidneys, termed bilateral disease, found in only 5–8% of cases. Management...

Alternative Titles

Full title

Bilateral Wilms tumour: a review of clinical and molecular features

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_5687181

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_5687181

Other Identifiers

ISSN

1462-3994

E-ISSN

1462-3994

DOI

10.1017/erm.2017.8

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