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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1986 1
1990 1
1999 1
2001 1
2003 2
2006 1
2010 2
2011 1
2012 1
2017 2
2019 1
2020 1
2021 1
2022 1
2024 0

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Page 1
Management of bilateral Wilms tumours.
Millar AJ, Cox S, Davidson A. Millar AJ, et al. Pediatr Surg Int. 2017 Apr;33(4):461-469. doi: 10.1007/s00383-016-4047-2. Epub 2017 Jan 4. Pediatr Surg Int. 2017. PMID: 28054101 Review.
Wilms tumour is named after Max Wilms. It is an embryonal tumour derived from the metanephros. ...For both synchronous and metachronous Wilms tumours the prognosis is less favourable with reported cure rates approaching 80% in the best centres and lowe
Wilms tumour is named after Max Wilms. It is an embryonal tumour derived from the metanephros. ...For both synchronous and
Management of bilateral Wilms tumours.
Millar AJW, Cox S, Davidson A. Millar AJW, et al. Pediatr Surg Int. 2017 Jul;33(7):737-745. doi: 10.1007/s00383-017-4091-6. Epub 2017 May 17. Pediatr Surg Int. 2017. PMID: 28516188 Review.
Wilms tumour is named after Max Wilms. It is an embryonal tumour derived from the metanephros. It is the commonest childhood renal tumour and the third commonest paediatric malignancy. Synchronous bilateral Wilms tumours (BWT) represent 4-7% of all Wilms
Wilms tumour is named after Max Wilms. It is an embryonal tumour derived from the metanephros. It is the commonest childhood r
Neonatal renal tumours.
Powis M. Powis M. Early Hum Dev. 2010 Oct;86(10):607-12. doi: 10.1016/j.earlhumdev.2010.08.018. Early Hum Dev. 2010. PMID: 20888153 Review.
Neonatal renal tumours are rare, with only 7% of all neonatal tumours arising from the kidney. Presentation is usually as a flank mass or as a coincidental finding on either antenatal or postnatal ultrasound. ...Given the low malignant potential of these tumours, treatment …
Neonatal renal tumours are rare, with only 7% of all neonatal tumours arising from the kidney. Presentation is usually as a flank mas …
Wilms' tumor metastatic to bilateral testes at presentation: case and review of the literature.
Palmer BW, Xiong Y, Gherezghiher A, Buethe D, Metwalli A, Frimberger D, Kropp BP. Palmer BW, et al. Urology. 2012 Apr;79(4):899-901. doi: 10.1016/j.urology.2011.08.057. Epub 2011 Nov 16. Urology. 2012. PMID: 22088565 Review.
A 7-year-old male with bilateral palpable testicular masses was found to have metastatic stage IV Wilms' tumors associated with both left renal and lung lesions. The patient was treated successfully with testicular-sparing bilateral partial orchiectomies, radical nephrecto …
A 7-year-old male with bilateral palpable testicular masses was found to have metastatic stage IV Wilms' tumors associated with both …
Nephrogenic rests, nephroblastomatosis, and the pathogenesis of Wilms' tumor.
Beckwith JB, Kiviat NB, Bonadio JF. Beckwith JB, et al. Pediatr Pathol. 1990;10(1-2):1-36. doi: 10.3109/15513819009067094. Pediatr Pathol. 1990. PMID: 2156243 Review.
A new classification and terminology is proposed for precursor lesions of Wilms' tumor (WT), based upon morphology and natural history. The generic term nephrogenic rest (NR) is used for all WT precursors. ...PLNRs were strongly associated with synchronous bilateral …
A new classification and terminology is proposed for precursor lesions of Wilms' tumor (WT), based upon morphology and natural …
[Tumor predisposition syndromes and nephroblastoma : Early diagnosis with imaging].
Welter N, Furtwängler R, Schneider G, Graf N, Schenk JP. Welter N, et al. Radiologie (Heidelb). 2022 Dec;62(12):1033-1042. doi: 10.1007/s00117-022-01056-w. Epub 2022 Aug 25. Radiologie (Heidelb). 2022. PMID: 36008692 Review. German.
CLINICAL/METHODICAL ISSUE: The Beckwith-Wiedemann spectrum (BWSp) as well as the WT1-related syndromes, Denys-Drash syndrome (DDS) and WAGR spectrum (Wilms tumor, Aniridia, genitourinary anomalies and a range of developmental delays) are tumor predisposition …
CLINICAL/METHODICAL ISSUE: The Beckwith-Wiedemann spectrum (BWSp) as well as the WT1-related syndromes, Denys-Drash syndrome (DDS) and WAGR …
Bilateral Wilms' tumors: single-center experience with 22 cases and literature review.
Sarhan OM, El-Baz M, Sarhan MM, Ghali AM, Ghoneim MA. Sarhan OM, et al. Urology. 2010 Oct;76(4):946-51. doi: 10.1016/j.urology.2010.03.055. Epub 2010 Aug 13. Urology. 2010. PMID: 20708784 Review.
OBJECTIVES: Bilateral Wilms' tumors represent a therapeutic challenge. The primary aim of management is eradication of the neoplasm and preservation of renal function. ...All patients had good renal function during follow-up, except for 1 patient who had undergone bilatera …
OBJECTIVES: Bilateral Wilms' tumors represent a therapeutic challenge. The primary aim of management is eradication of the neoplasm a …
Surgical treatment of pulmonary metastases in childhood.
Winkler K. Winkler K. Thorac Cardiovasc Surg. 1986 Nov;34 Spec No 2:133-6. doi: 10.1055/s-2007-1022190. Thorac Cardiovasc Surg. 1986. PMID: 2432685 Review.
Of all tumors occurring in childhood and adolescence only osteosarcoma, Wilms tumor and Ewing's sarcoma preferentially disseminate to the lungs and such are the most promising candidates for successful treatment. ...Although metachronous lung metastases may s …
Of all tumors occurring in childhood and adolescence only osteosarcoma, Wilms tumor and Ewing's sarcoma preferentially dissemi …
Clinicopathologic features of nephrogenic rests and nephroblastomatosis.
Hennigar RA, O'Shea PA, Grattan-Smith JD. Hennigar RA, et al. Adv Anat Pathol. 2001 Sep;8(5):276-89. doi: 10.1097/00125480-200109000-00005. Adv Anat Pathol. 2001. PMID: 11556536 Review.
Evidence strongly suggests that neoplastic transformation of nephrogenic rests results in Wilms' tumor (nephroblastoma). Nephrogenic rests almost always occur in the setting of Wilms' tumor; perilobar rests show a strong association with synchronous bi …
Evidence strongly suggests that neoplastic transformation of nephrogenic rests results in Wilms' tumor (nephroblastoma). Nephr …
Wilms Tumor Associated With the 9q22.3 Microdeletion Syndrome: 2 New Case Reports and a Review of The Literature.
Cayrol J, Nightingale M, Challis J, Campbell M, Sullivan M, Heloury Y. Cayrol J, et al. J Pediatr Hematol Oncol. 2019 Nov;41(8):e517-e520. doi: 10.1097/MPH.0000000000001322. J Pediatr Hematol Oncol. 2019. PMID: 30371535 Review.
It encompasses the PTCH1 gene locus that harbors mutations for GS. Although the 9q22.3 syndrome is associated with Wilms tumor (WT), WT is not a GS-associated tumor, implying a different mechanism involving PTCH1, or a different locus in the 9q22.3 region. .. …
It encompasses the PTCH1 gene locus that harbors mutations for GS. Although the 9q22.3 syndrome is associated with Wilms tumor
15 results