Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My NCBI Filters

Results by year

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

Year Number of Results
1934 1
1938 1
1943 1
1944 1
1945 2
1946 9
1947 9
1948 11
1949 15
1950 10
1951 12
1952 13
1953 19
1954 20
1955 20
1956 26
1957 21
1958 19
1959 28
1960 25
1961 31
1962 35
1963 49
1964 86
1965 66
1966 63
1967 83
1968 127
1969 112
1970 116
1971 125
1972 126
1973 148
1974 164
1975 137
1976 158
1977 128
1978 147
1979 144
1980 168
1981 173
1982 183
1983 162
1984 182
1985 181
1986 167
1987 195
1988 198
1989 251
1990 220
1991 238
1992 301
1993 295
1994 254
1995 301
1996 304
1997 269
1998 289
1999 264
2000 246
2001 235
2002 236
2003 271
2004 253
2005 262
2006 292
2007 293
2008 319
2009 312
2010 351
2011 349
2012 356
2013 395
2014 416
2015 391
2016 377
2017 352
2018 405
2019 413
2020 418
2021 441
2022 476
2023 409
2024 241

Text availability

Article attribute

Article type

Publication date

Search Results

14,455 results

Results by year

Filters applied: . Clear all
Page 1
Wilms tumor.
Friedman AD. Friedman AD. Pediatr Rev. 2013 Jul;34(7):328-30; discussion 330. doi: 10.1542/pir.34-7-328. Pediatr Rev. 2013. PMID: 23818087 Review. No abstract available.
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 translational a
Wilms' tumor or nephroblastoma is the most frequent renal tumor in children and is associated with different congenital
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
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 …
Wilms' tumour 1 (WT1) in development, homeostasis and disease.
Hastie ND. Hastie ND. Development. 2017 Aug 15;144(16):2862-2872. doi: 10.1242/dev.153163. Development. 2017. PMID: 28811308 Free article. Review.
The study of genes mutated in human disease often leads to new insights into biology as well as disease mechanisms. One such gene is Wilms' tumour 1 (WT1), which plays multiple roles in development, tissue homeostasis and disease. ...
The study of genes mutated in human disease often leads to new insights into biology as well as disease mechanisms. One such gene is Wilm
Wilms tumour.
[No authors listed] [No authors listed] Nat Rev Dis Primers. 2021 Oct 14;7(1):76. doi: 10.1038/s41572-021-00315-9. Nat Rev Dis Primers. 2021. PMID: 34650083 No abstract available.
Genetic variation frequencies in Wilms' tumor: A meta-analysis and systematic review.
Deng C, Dai R, Li X, Liu F. Deng C, et al. Cancer Sci. 2016 May;107(5):690-9. doi: 10.1111/cas.12910. Epub 2016 Mar 18. Cancer Sci. 2016. PMID: 26892980 Free PMC article. Review.
Over the last few decades, numerous biomarkers in Wilms' tumor have been confirmed and shown variations in prevalence. ...The limited prevalence of currently known genetic alterations in Wilms' tumors indicates that significant drivers of initiation and progr …
Over the last few decades, numerous biomarkers in Wilms' tumor have been confirmed and shown variations in prevalence. ...The …
Phylogeny of Wilms tumor?
Charles A. Charles A. EBioMedicine. 2016 Jul;9:11-12. doi: 10.1016/j.ebiom.2016.06.044. Epub 2016 Jul 4. EBioMedicine. 2016. PMID: 27453324 Free PMC article. No abstract available.
Adult Wilms' tumor.
Sharma MS, Ahmed MZ. Sharma MS, et al. Saudi J Kidney Dis Transpl. 2009 Sep;20(5):835-7. Saudi J Kidney Dis Transpl. 2009. PMID: 19736484
Adult Wilms' Tumor (AWT) is a rare entity arising from the metanephric blastema. ...The staging of AWT is done in the same way as in children according to the National Wilms' Tumour Stage Group (NWTSG). Definitive treatment plans for AWT are undefined …
Adult Wilms' Tumor (AWT) is a rare entity arising from the metanephric blastema. ...The staging of AWT is done in the same way …
Robot-assisted radical nephrectomy for Wilms' tumor in children.
Van Der Jeugt J, Jamaer C, Berquin C, Decaestecker K, Hoebeke P, Van Laecke E, Van Praet C, Spinoit AF. Van Der Jeugt J, et al. J Pediatr Urol. 2023 Aug;19(4):489-490. doi: 10.1016/j.jpurol.2023.04.016. Epub 2023 Apr 18. J Pediatr Urol. 2023. PMID: 37130763
INTRODUCTION: Surgical removal of the tumor is a key step in the management of nephroblastoma. Less invasive surgical approaches such as robot-assisted radical nephrectomy (RARN) has gained momentum over the past few years. ...
INTRODUCTION: Surgical removal of the tumor is a key step in the management of nephroblastoma. Less invasive surgical approaches such …
14,455 results
You have reached the last available page of results. Please see the User Guide for more information.