An edition of Wilms Tumor (2016)

Wilms Tumor

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Last edited by openaccessresearcher
December 20, 2017 | History
An edition of Wilms Tumor (2016)

Wilms Tumor

  • 0 Ratings
  • 1 Want to read
  • 1 Currently reading
  • 0 Have read

Wilms tumor is a rare kidney cancer that is usually diagnosed in children under the age of six. Wilms tumor is mostly the result of aberrations in WT1 gene, located on chromosome 11p13. In addition to being a risk factor for Wilms tumor, WT1 aberrations cause extra renal complications and other malignancies. This book brings together the basic and clinical aspects of Wilms tumor and WT1 research under three sections. Section I provides a comprehensive guide to the epidemiology, diagnostics, management, and treatment of Wilms tumor. Section II covers the biological aspects of Wilms tumor and WT1. Section III focuses on the role of WT1 in cardiac development, prostate cancer, glioblastoma and minimal residual disease.

Contributors: 64; Chapters: 16; Figures: 50; Tables: 20; Pages: 294

Publish Date
Publisher
Codon Publications
Language
English
Pages
294

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Previews available in: English

Edition Availability
Cover of: Wilms Tumor
Wilms Tumor
2016 Mar, Codon Publications
Hardcover in English

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Book Details


Table of Contents

Foreword
Preface
Contributors
Section I. Epidemiology, Diagnostics, and Treatment
1. Wilms’ Tumour – Histology and Differential Diagnosis
2. The Clinical Relevance of Age at Presentation in Nephroblastoma
3. Histopathological and Molecular Characteristics of Wilms Tumor
4. Wilms Tumor and Its Management in a Surgical Aspect
5. Management of Bilateral Wilms Tumours
6. Extrarenal Wilms’ Tumor: Challenges in Diagnosis, Embryology, Treatment and Prognosis
7. Neoadjuvant Transcatheter Arterial Chemoembolization and Systemic Chemotherapy for the Treatment of Wilms Tumor
8. Dendritic Cell-Based Cancer Immunotherapy Targeting Wilms’ Tumor 1 for Pediatric Cancer
9. Chronic Kidney Disease in Wilms Tumour Survivors – What Do We Know Today?
Section II. Biology
10. Gene Expression in Wilms Tumor: Disturbance of the Wnt Signaling Pathway and MicroRNA Biogenesis
11. Transcriptional Regulation of the Human Thromboxane A2 Receptor Gene by Wilms’ Tumour (WT)1
12. The Inflammatory Microenvironment in Wilms Tumors
Section III. WT1 Gene Aberrations in Other Malignancies
13. WT1 in Cardiac Development and Disease
15. Functional Roles of Wilms’ Tumor 1 (WT1) in Malignant Brain Tumors
16. Wilms’ Tumor Gene (WT1) Expression and Minimal Residual Disease in Acute Myeloid Leukemia
Index

Edition Notes

Copyright © 2016 Codon Publications.
Published under Creative Commons Attribution 4.0 International (CC BY 4.0). Users are allowed to share (copy and redistribute the material in any medium or format) and adapt (remix, transform, and build upon the material for any purpose, even commercially), as long as the authors and the publisher are explicitly identified and properly acknowledged as the original source.

Published in
Brisbane, Australia
Other Titles
Wilms' Tumour

Classifications

Dewey Decimal Class
616.994

Contributors

Editor
Marry M. van den Heuvel-Eibrink

The Physical Object

Format
Hardcover
Pagination
294p
Number of pages
294
Dimensions
10 x 7.3 x 1 inches
Weight
2.2 pounds

ID Numbers

Open Library
OL26407797M
Internet Archive
NBK373360
ISBN 10
0994438117
ISBN 13
9780994438119
OCLC/WorldCat
958942477
Google
sdn2jwEACAAJ
Library Thing
20775590
Goodreads
37531623

Work Description

This book focuses on Childhood Cancer, specifically Wilms Tumor. It is the work of 64 contributors and has been written to cover diagnosis and treatment of the disease with modern techniques. This is written for Oncologists, Hematologists and Pathologists.

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History

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December 20, 2017 Edited by openaccessresearcher Metatag
December 15, 2017 Edited by openaccessresearcher NCBI linked publication
December 15, 2017 Edited by openaccessresearcher Edited without comment.
December 15, 2017 Edited by openaccessresearcher Edited without comment.
December 15, 2017 Created by openaccessresearcher Added new book.