(Q45721933)

15 December 2017

Outcome of pediatric renal tumor treated using the Japan Wilms Tumor Study-1 (JWiTS-1) protocol: a report from the JWiTS group (English)

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15 December 2017

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Takaharu Oue

1

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15 December 2017

Masahiro Fukuzawa

2

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15 December 2017

Hajime Okita

3

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15 December 2017

Hideo Mugishima

4

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15 December 2017

Hiroshi Horie

5

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15 December 2017

Jun-ichi Hata

6

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15 December 2017

Masahiro Saito

7

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15 December 2017

Miwako Nozaki

8

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15 December 2017

Motoaki Chin

9

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15 December 2017

Hisaya Nakadate

10

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15 December 2017

Shiro Hinotsu

11

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15 December 2017

Tsugumichi Koshinaga

12

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15 December 2017

Yasuhiko Kaneko

13

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15 December 2017

Yoshihiro Kitano

14

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15 December 2017

Yukichi Tanaka

15

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15 December 2017

Japan Wilms Tumor Study (JWiTS) Group

16

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15 December 2017

1 November 2009

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Pediatric Surgery International

15 December 2017

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15 December 2017

25

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15 December 2017

11

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15 December 2017

923-929

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https://scigraph.springernature.com/pub.10.1007/s00383-009-2449-0

15 December 2017

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cites work

Ultrastructure of malignant rhabdoid tumor of the kidney. A distinctive renal tumor of children

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12 December 2020

Radiotherapy in the SIOP (International Society of Pediatric Oncology) nephroblastoma studies: a review

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12 December 2020

Immediate nephrectomy versus preoperative chemotherapy in the management of non-metastatic Wilms' tumour: results of a randomised trial (UKW3) by the UK Children's Cancer Study Group

1 reference

12 December 2020

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

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12 December 2020

Reduction of postoperative chemotherapy in children with stage I intermediate-risk and anaplastic Wilms' tumour (SIOP 93-01 trial): a randomised controlled trial

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12 December 2020

Rhabdoid tumor of kidney. A report of 111 cases from the National Wilms' Tumor Study Pathology Center

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12 December 2020

Treatment with nephrectomy only for small, stage I/favorable histology Wilms' tumor: a report from the National Wilms' Tumor Study Group

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12 December 2020

The National Wilms Tumor Study: a 40 year perspective

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12 December 2020

Extended followup of bilateral Wilms tumor: results of the National Wilms Tumor Study.

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12 December 2020

Bilateral Wilms tumor

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12 December 2020

Clear cell sarcoma of the kidney with emphasis on ultrastructural studies

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12 December 2020

Histopathology and prognosis of Wilms tumorResults from the first national wilms' tumor study

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12 December 2020

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12 December 2020

Current issues in Wilms tumor management

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12 December 2020

Duplication of paternal IGF2 or loss of maternal IGF2 imprinting occurs in half of Wilms tumors with various structural WT1 abnormalities

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12 December 2020

High telomerase RNA expression level is an adverse prognostic factor for favorable-histology Wilms' tumor.

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12 December 2020

Survival in bilateral Wilms' tumor—Review of 30 National Wilms' Tumor Study cases

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12 December 2020

The treatment of Wilms' tumor. Results of the national Wilms' tumor study

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12 December 2020

Combined BubR1 protein down-regulation and RASSF1A hypermethylation in Wilms tumors with diverse cytogenetic changes.

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12 December 2020

Loss of heterozygosity for chromosomes 1p and 16q is an adverse prognostic factor in favorable-histology Wilms tumor: a report from the National Wilms Tumor Study Group

1 reference

12 December 2020

Treatment of children with clear-cell sarcoma of the kidney: a report from the National Wilms' Tumor Study Group

1 reference

12 December 2020

Association of 11q loss, trisomy 12, and possible 16q loss with loss of imprinting of insulin-like growth factor-II in Wilms tumor

1 reference

12 December 2020

10.1007/S00383-009-2449-0

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DOI

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Dimensions Publication ID

15 December 2017

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