(Q37738817)

22 August 2017

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title

Current management of wilms' tumor (English)

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22 August 2017

Leah Nakamura

1

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22 August 2017

Michael Ritchey

series ordinal

2

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22 August 2017

publication date

1 February 2010

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22 August 2017

published in

Current urology reports

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22 August 2017

volume

11

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22 August 2017

issue

1

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22 August 2017

page(s)

58-65

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https://scigraph.springernature.com/pub.10.1007/s11934-009-0082-z

22 August 2017

exact match

0 references

cites work

Treatment outcomes in adults with favorable histologic type Wilms tumor-an update from the National Wilms Tumor Study Group

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FS11934-009-0082-Z

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

21 January 2018

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12 December 2020

Loss of 11q and 16q in Wilms tumors is associated with anaplasia, tumor recurrence, and poor prognosis

1 reference

12 December 2020

Bilateral Wilms' tumors with progressive or nonresponsive disease

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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

The feasibility and outcome of nephron-sparing surgery for children with bilateral Wilms tumor. The St Jude Children's Research Hospital experience: 1999-2006.

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12 December 2020

Treatment of anaplastic histology Wilms' tumor: results from the fifth National Wilms' Tumor Study.

1 reference

12 December 2020

Optimal duration of preoperative therapy in unilateral and nonmetastatic Wilms' tumor in children older than 6 months: results of the Ninth International Society of Pediatric Oncology Wilms' Tumor Trial and Study

1 reference

12 December 2020

Fate of bilateral renal lesions missed on preoperative imaging: a report from the National Wilms Tumor Study Group

1 reference

12 December 2020

Denys-Drash syndrome: relating a clinical disorder to genetic alterations in the tumor suppressor gene WT1

1 reference

12 December 2020

Role of MRI in the management of patients with nephroblastoma

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12 December 2020

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

1 reference

12 December 2020

Predicting relapse in favorable histology Wilms tumor using gene expression analysis: a report from the Renal Tumor Committee of the Children's Oncology Group

1 reference

12 December 2020

Loss of Imprinting of Insulin-Like Growth Factor-II (IGF2) Gene in Distinguishing Specific Biologic Subtypes of Wilms Tumor

1 reference

12 December 2020

Intravascular Extension of Wilms Tumor

1 reference

12 December 2020

Raised risk of Wilms tumour in patients with aniridia and submicroscopic WT1 deletion

1 reference

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

1 reference

12 December 2020

Results of the SIOP 93-01/GPOH trial and study for the treatment of patients with unilateral nonmetastatic Wilms Tumor.

1 reference

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

Late effects of treatment for wilms tumor

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12 December 2020

Allele loss at 16q defines poorer prognosis Wilms tumour irrespective of treatment approach in the UKW1-3 clinical trials: a Children's Cancer and Leukaemia Group (CCLG) Study

1 reference

12 December 2020

An X chromosome gene, WTX, is commonly inactivated in Wilms tumor

1 reference

12 December 2020

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.

1 reference

12 December 2020

Hyperplastic perilobar nephroblastomatosis: long-term survival of 52 patients.

1 reference

12 December 2020

Renal failure in the Denys-Drash and Wilms' tumor-aniridia syndromes

1 reference

12 December 2020

Rarity of surgical complications after postchemotherapy nephrectomy for nephroblastoma. Experience of the International Society of Paediatric Oncology-Trial and Study "SIOP-9". International Society of Paediatric Oncology Nephroblastoma Trial and St

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12 December 2020

Early and late mortality after diagnosis of wilms tumor

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12 December 2020

The treatment of Wilms' tumour: results of the United Kingdom Children's cancer study group (UKCCSG) second Wilms' tumour study

1 reference

12 December 2020

Partial nephrectomy for unilateral Wilms tumor: results of study SIOP 93-01/GPOH.

1 reference

12 December 2020

Bilateral Wilms' tumor with anaplasia: lessons from the National Wilms' Tumor Study.

1 reference

12 December 2020

Renal function adaptation in children with unilateral renal tumors treated with nephron sparing surgery or nephrectomy

1 reference

12 December 2020

Increased tissue factor expression and poor nephroblastoma prognosis.

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12 December 2020

Wilms tumour histology is determined by distinct types of precursor lesions and not epigenetic changes

1 reference

12 December 2020

Characteristics and outcomes of children with the Wilms tumor-Aniridia syndrome: a report from the National Wilms Tumor Study Group

1 reference

12 December 2020

Intraoperative spillage of favorable histology wilms tumor cells: influence of irradiation and chemotherapy regimens on abdominal recurrence. A report from the National Wilms Tumor Study Group

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12 December 2020

Screening for Wilms tumor in children with Beckwith-Wiedemann syndrome or idiopathic hemihypertrophy

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12 December 2020

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12 December 2020

Small glomeruli in WAGR (Wilms Tumor, Aniridia, Genitourinary Anomalies and Mental Retardation) syndrome.

1 reference

12 December 2020

Characteristics and outcome of children with Beckwith-Wiedemann syndrome and Wilms' tumor: a report from the National Wilms Tumor Study Group

1 reference

12 December 2020

Synchronous bilateral Wilm's tumor with complete radiographic response managed without surgical resection: a report from the National Wilm's Tumor Study 4.

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12 December 2020

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12 December 2020

The role of biopsy in the diagnosis of renal tumors of childhood: Results of the UKCCSG Wilms tumor study 3.

1 reference

12 December 2020

Factors affecting the risk of contralateral Wilms tumor development: a report from the National Wilms Tumor Study Group

1 reference

12 December 2020

Renin-induced hypertension in Wilms tumor patients

1 reference

12 December 2020

Laparoscopic nephrectomy for Wilms' tumor.

1 reference

12 December 2020

Nephrogenic rests and the pathogenesis of Wilms tumor: developmental and clinical considerations

1 reference

12 December 2020

Treatment of Wilms tumor relapsing after initial treatment with vincristine, actinomycin D, and doxorubicin. A report from the National Wilms Tumor Study Group

1 reference

12 December 2020

Frequency and Heritability ofWT1Mutations in Nonsyndromic Wilms' Tumor Patients: A UK Children’s Cancer Study Group Study

1 reference

12 December 2020

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

1 reference

12 December 2020

Ureteral extension in Wilms' tumor: a report from the National Wilms' Tumor Study Group (NWTSG).

1 reference

12 December 2020

New insights into the function of the Wilms tumor suppressor gene WT1 in podocytes

1 reference

12 December 2020

Pediatric renal tumors: practical updates for the pathologist

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12 December 2020

Prechemotherapy laparoscopic nephrectomy for Wilms' tumor

1 reference

12 December 2020

End stage renal disease in patients with Wilms tumor: results from the National Wilms Tumor Study Group and the United States Renal Data System

1 reference

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

Wilms tumor genetics: mutations in WT1, WTX, and CTNNB1 account for only about one-third of tumors

1 reference

12 December 2020

Nephromegaly in infancy and early childhood: a risk factor for Wilms tumor in Beckwith-Wiedemann syndrome

1 reference

12 December 2020

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

1 reference

12 December 2020

10.1007/S11934-009-0082-Z

Identifiers

DOI

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22 August 2017

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