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

Year Number of Results
1964 1
1965 3
1967 3
1968 3
1969 7
1970 3
1971 10
1972 10
1973 14
1974 16
1975 5
1976 6
1977 11
1978 7
1979 3
1980 6
1981 13
1982 9
1983 10
1984 14
1985 21
1986 16
1987 21
1988 35
1989 39
1990 21
1991 44
1992 58
1993 65
1994 43
1995 69
1996 42
1997 52
1998 54
1999 47
2000 41
2001 45
2002 36
2003 40
2004 35
2005 52
2006 40
2007 40
2008 38
2009 36
2010 35
2011 27
2012 47
2013 33
2014 44
2015 51
2016 38
2017 42
2018 30
2019 50
2020 31
2021 36
2022 48
2023 47
2024 20

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1,665 results

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Page 1
Wilms tumor.
Pater L, Melchior P, Rübe C, Cooper BT, McAleer MF, Kalapurakal JA, Paulino AC. Pater L, et al. Pediatr Blood Cancer. 2021 May;68 Suppl 2:e28257. doi: 10.1002/pbc.28257. Epub 2020 Sep 7. Pediatr Blood Cancer. 2021. PMID: 32893998 Review.
The objectives for the treatment of Wilms tumor in both the Children's Oncology Group (COG) and the International Society of Paediatric Oncology (SIOP) have focused on improving cure rates and minimizing toxicity by limiting the use of radiation and doxorubicin. ... …
The objectives for the treatment of Wilms tumor in both the Children's Oncology Group (COG) and the International Society of P …
Wilms tumour.
Spreafico F, Fernandez CV, Brok J, Nakata K, Vujanic G, Geller JI, Gessler M, Maschietto M, Behjati S, Polanco A, Paintsil V, Luna-Fineman S, Pritchard-Jones K. Spreafico F, et al. Nat Rev Dis Primers. 2021 Oct 14;7(1):75. doi: 10.1038/s41572-021-00308-8. Nat Rev Dis Primers. 2021. PMID: 34650095 Review.
Wilms tumour (WT) is a childhood embryonal tumour that is paradigmatic of the intersection between disrupted organogenesis and tumorigenesis. ...
Wilms tumour (WT) is a childhood embryonal tumour that is paradigmatic of the intersection between disrupted organogenesis and tumori
Wilms Tumor.
Saltzman AF, Cost NG, Romao RLP. Saltzman AF, et al. Urol Clin North Am. 2023 Aug;50(3):455-464. doi: 10.1016/j.ucl.2023.04.008. Epub 2023 May 18. Urol Clin North Am. 2023. PMID: 37385707 Review.
Wilms tumor (WT), or nephroblastoma, is the most common primary malignant renal tumor of childhood. It is an embryonal tumor that develops from remnants of immature kidney. There are approximately 500 new WT cases diagnosed in the United States
Wilms tumor (WT), or nephroblastoma, is the most common primary malignant renal tumor of childhood. It is an emb
Update on Wilms tumor.
Aldrink JH, Heaton TE, Dasgupta R, Lautz TB, Malek MM, Abdessalam SF, Weil BR, Rhee DS, Baertschiger R, Ehrlich PF; American Pediatric Surgical Association Cancer Committee. Aldrink JH, et al. J Pediatr Surg. 2019 Mar;54(3):390-397. doi: 10.1016/j.jpedsurg.2018.09.005. Epub 2018 Sep 19. J Pediatr Surg. 2019. PMID: 30270120 Free PMC article. Review.
This article reviews of the current evidence-based treatment standards for children with Wilms tumor. In this article, a summary of recently completed clinical trials by the Children's Oncology Group is provided, the current diagnostic evaluation and surgical standa …
This article reviews of the current evidence-based treatment standards for children with Wilms tumor. In this article, a summa …
The UMBRELLA SIOP-RTSG 2016 Wilms tumour pathology and molecular biology protocol.
Vujanić GM, Gessler M, Ooms AHAG, Collini P, Coulomb-l'Hermine A, D'Hooghe E, de Krijger RR, Perotti D, Pritchard-Jones K, Vokuhl C, van den Heuvel-Eibrink MM, Graf N; International Society of Paediatric Oncology–Renal Tumour Study Group (SIOP–RTSG). Vujanić GM, et al. Nat Rev Urol. 2018 Nov;15(11):693-701. doi: 10.1038/s41585-018-0100-3. Nat Rev Urol. 2018. PMID: 30310143 Free PMC article.
On the basis of the results of previous national and international trials and studies, the Renal Tumour Study Group of the International Society of Paediatric Oncology (SIOP-RTSG) has developed a new study protocol for paediatric renal tumours: the UMBRELLA SIOP-RTSG 2016 protoco …
On the basis of the results of previous national and international trials and studies, the Renal Tumour Study Group of the International Soc …
New approaches to risk stratification for Wilms tumor.
Nelson MV, van den Heuvel-Eibrink MM, Graf N, Dome JS. Nelson MV, et al. Curr Opin Pediatr. 2021 Feb 1;33(1):40-48. doi: 10.1097/MOP.0000000000000988. Epub 2020 Dec 29. Curr Opin Pediatr. 2021. PMID: 33394739 Free PMC article. Review.
PURPOSE OF REVIEW: The treatment of Wilms tumor is one of the great achievements in the field of oncology. ...This article highlights the evolution of clinical and biological prognostic markers that have been applied in the treatment of Wilms tumor. RE …
PURPOSE OF REVIEW: The treatment of Wilms tumor is one of the great achievements in the field of oncology. ...This article hig …
Neuroblastoma and nephroblastoma: a radiological review.
Dumba M, Jawad N, McHugh K. Dumba M, et al. Cancer Imaging. 2015 Apr 8;15(1):5. doi: 10.1186/s40644-015-0040-6. Cancer Imaging. 2015. PMID: 25889326 Free PMC article. Review.
It can present as an abdominal mass, but is usually metastatic at diagnosis so the symptomatology can be varied. Nephroblastoma, also more commonly known as a Wilms tumour, is the commonest renal tumour in childhood and more typically presents as abdominal pathology …
It can present as an abdominal mass, but is usually metastatic at diagnosis so the symptomatology can be varied. Nephroblastoma, also …
Neonatal Renal Tumors.
Sze SK. Sze SK. Clin Perinatol. 2021 Mar;48(1):71-81. doi: 10.1016/j.clp.2020.11.004. Epub 2021 Jan 11. Clin Perinatol. 2021. PMID: 33583508 Review.
Wilms' tumor.
Martínez CH, Dave S, Izawa J. Martínez CH, et al. Adv Exp Med Biol. 2010;685:196-209. Adv Exp Med Biol. 2010. PMID: 20687507 Review.
Wilms' tumor or nephroblastoma is the most frequent renal tumor in children and is associated with different congenital anomalies and syndromes. ...Our aim with this chapter of Wilms' tumor is to present the state of knowledge in translat
Wilms' tumor or nephroblastoma is the most frequent renal tumor in children and is associated with different con
Pediatric genitourinary tumors.
Castellino SM, McLean TW. Castellino SM, et al. Curr Opin Oncol. 2007 May;19(3):248-53. doi: 10.1097/CCO.0b013e3280ad43ce. Curr Opin Oncol. 2007. PMID: 17414644 Review.
The addition of more intensive chemotherapy for anaplastic histology disease, recognition of loss of heterozygosity for chromosomes 1p and 16q as an adverse prognostic factor in favorable histology Wilms' tumor, and the utilization of molecular markers to better cha …
The addition of more intensive chemotherapy for anaplastic histology disease, recognition of loss of heterozygosity for chromosomes 1p and 1 …
1,665 results