(Q34238246)

31 July 2017

title

Clinical impact of histologic subtypes in localized non-anaplastic nephroblastoma treated according to the trial and study SIOP-9/GPOH. (English)

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31 July 2017

N Graf

7

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author name string

A Weirich

1

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31 July 2017

I Leuschner

2

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31 July 2017

D Harms

3

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31 July 2017

G M Vujanic

4

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31 July 2017

J Tröger

5

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31 July 2017

U Abel

6

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31 July 2017

D Schmidt

8

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31 July 2017

R Ludwig

9

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31 July 2017

P A Voûte

10

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31 July 2017

publication date

1 March 2001

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31 July 2017

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31 July 2017

volume

12

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31 July 2017

issue

3

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31 July 2017

page(s)

311-319

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Renal tumours of childhood

31 July 2017

cites work

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The relationship between microsubstaging variables, age at diagnosis, and tumor weight of children with stage I/favorable histology Wilms' tumor. A report from the National Wilms' Tumor study

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Complete necrosis induced by preoperative chemotherapy in Wilms tumor as an indicator of low risk: report of the international society of paediatric oncology (SIOP) nephroblastoma trial and study 9.

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Malignant renal tumors of childhood

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Durchführung eines neuen Therapiekonzepts für Nephroblastome im Bereich der Gesellschaft für Pädiatrische Onkologie und Hämatologie SIOP 9/GPOH

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[Preoperative chemotherapy of nephroblastoma. Preliminary results of the SIOP-9/GPO therapy study]

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Design and analysis of randomized clinical trials requiring prolonged observation of each patient. II. analysis and examples

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The effect of preoperative therapy on the histologic features of Wilms' tumor. An analysis of cases from the Third National Wilms' Tumor Study

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Prognostic factors in nonmetastatic, favorable histology Wilms' tumor. Results of the Third National Wilms' Tumor Study

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Histological analysis of aggressiveness and responsiveness in Wilms' tumor

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Fetal rhabdomyomatous nephroblastoma. Pathologic histology and special clinical and biologic features

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Fetal rhabdomyomatous nephroblastoma: a tumour of good prognosis but resistant to chemotherapy

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Cellular differentiation and prognosis in embryonal rhabdomyosarcoma. A report from the Cooperative Soft Tissue Sarcoma Study 1981 (CWS 81)

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Hepatic rhabdomyomatous tumor: late sequel of a fetal rhabdomyomatous nephroblastoma

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Bilateral rhabdomyomatous tumor relapsed as typical triphasic Wilms' tumor

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Correlation of germ-line mutations and two-hit inactivation of the WT1 gene with Wilms tumors of stromal-predominant histology

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7 January 2021

Loss of WT1 function leads to ectopic myogenesis in Wilms' tumour

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7 January 2021

Nephroblastoma (Wilms tumor): Tubule density and prognosis

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7 January 2021

Massive Wilms' tumor: sonographic demonstration of therapeutic response without alteration in size

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7 January 2021

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Identifiers

DOI

10.1023/A:1011167924230

1 reference

31 July 2017

1 reference