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 Custom Filters

Results by year

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

Year Number of Results
1925 1
1946 4
1947 2
1948 6
1949 3
1950 5
1951 13
1952 7
1953 14
1954 11
1955 9
1956 8
1957 11
1958 11
1959 6
1960 10
1961 9
1962 15
1963 55
1964 65
1965 46
1966 58
1967 58
1968 71
1969 74
1970 66
1971 88
1972 98
1973 76
1974 104
1975 80
1976 88
1977 84
1978 82
1979 65
1980 65
1981 64
1982 70
1983 96
1984 112
1985 94
1986 110
1987 98
1988 94
1989 112
1990 111
1991 96
1992 124
1993 109
1994 108
1995 111
1996 123
1997 128
1998 149
1999 126
2000 132
2001 151
2002 130
2003 137
2004 146
2005 158
2006 172
2007 166
2008 180
2009 238
2010 214
2011 240
2012 240
2013 245
2014 256
2015 290
2016 247
2017 254
2018 266
2019 283
2020 337
2021 349
2022 313
2023 313
2024 296
2025 154

Publication date

Text availability

Article attribute

Article type

Additional filters

Article Language

Species

Sex

Age

Other

Search Results

8,673 results

Results by year

Filters applied: . Clear all
Page 1
Ependymoma: Evaluation and Management Updates.
Rudà R, Bruno F, Pellerino A, Soffietti R. Rudà R, et al. Curr Oncol Rep. 2022 Aug;24(8):985-993. doi: 10.1007/s11912-022-01260-w. Epub 2022 Apr 6. Curr Oncol Rep. 2022. PMID: 35384591 Free PMC article. Review.
PURPOSE OF REVIEW: To review state of art and relevant advances in the molecular genetics and management of ependymomas of children and adults. RECENT FINDINGS: Ependymomas may occur either in the brain or in the spinal cord. Compared with intracranial ependymoma
PURPOSE OF REVIEW: To review state of art and relevant advances in the molecular genetics and management of ependymomas of children a …
Ependymoma.
Gerstner ER, Pajtler KW. Gerstner ER, et al. Semin Neurol. 2018 Feb;38(1):104-111. doi: 10.1055/s-0038-1636503. Epub 2018 Mar 16. Semin Neurol. 2018. PMID: 29548057 Review.
Ependymoma can arise throughout the whole neuraxis. In children, tumors predominantly occur intracranially, whereas the spine is the most prevalent location in adults. ...Novel research strategies are currently applied for target discovery in ependymomas since for m
Ependymoma can arise throughout the whole neuraxis. In children, tumors predominantly occur intracranially, whereas the spine is the
Pediatric Ependymoma.
Vitanza NA, Partap S. Vitanza NA, et al. J Child Neurol. 2016 Oct;31(12):1354-66. doi: 10.1177/0883073815610428. Epub 2015 Oct 26. J Child Neurol. 2016. PMID: 26503805 Review.
Over the past 150 years since Virchow's initial characterization of ependymoma, incredible efforts have been made in the classification of these tumors and in the care of pediatric patients with this disease. ...This review includes and synthesizes the clinical understandi …
Over the past 150 years since Virchow's initial characterization of ependymoma, incredible efforts have been made in the classificati …
Ependymoma.
Reni M, Gatta G, Mazza E, Vecht C. Reni M, et al. Crit Rev Oncol Hematol. 2007 Jul;63(1):81-9. doi: 10.1016/j.critrevonc.2007.03.004. Epub 2007 May 4. Crit Rev Oncol Hematol. 2007. PMID: 17482475 Review.
Ependymomas are rare tumours of neuroectodermal origin classified as myxopapillary ependymoma and subependymoma (grade I), ependymoma (grade II) and anaplastic ependymoma (grade III). ...Postoperative radiotherapy is indicated in high-grade ependymo
Ependymomas are rare tumours of neuroectodermal origin classified as myxopapillary ependymoma and subependymoma (grade I),
[Precision Medicine for Ependymoma].
Gomi A. Gomi A. No Shinkei Geka. 2022 Jan;50(1):91-100. doi: 10.11477/mf.1436204534. No Shinkei Geka. 2022. PMID: 35169089 Review. Japanese.
Herein we discuss precision medicine for ependymoma. We reviewed the new molecular classifications of ependymoma, studies on the molecular mechanisms involved in carcinogenesis and proliferation, and the various studies exploring new therapeutic strategies. Of the n …
Herein we discuss precision medicine for ependymoma. We reviewed the new molecular classifications of ependymoma, studies on t …
Supratentorial and Infratentorial Ependymoma.
Myseros JS. Myseros JS. Adv Tech Stand Neurosurg. 2024;53:93-118. doi: 10.1007/978-3-031-67077-0_7. Adv Tech Stand Neurosurg. 2024. PMID: 39287805 Review.
Ependymomas are the third most common intracranial tumor in children, presenting in both the supratentorial and infratentorial compartments. ...On the contrary, older children with supratentorial YAP1 fusion-positive ependymomas and type B posterior fossa tumors may
Ependymomas are the third most common intracranial tumor in children, presenting in both the supratentorial and infratentorial compar
Pediatric ependymoma: an overview of a complex disease.
Jünger ST, Timmermann B, Pietsch T. Jünger ST, et al. Childs Nerv Syst. 2021 Aug;37(8):2451-2463. doi: 10.1007/s00381-021-05207-7. Epub 2021 May 18. Childs Nerv Syst. 2021. PMID: 34008056 Free PMC article. Review.
Pediatric ependymomas comprise biologically distinct tumor entities with different (epi)genetics, age distribution and localization, as well as a different prognosis. ...Current therapy achieves reasonable survival rates for the majority of ependymoma patients. The …
Pediatric ependymomas comprise biologically distinct tumor entities with different (epi)genetics, age distribution and localization, …
Orbital Ependymoma.
Tsimchi IM, Malik AI, Takashima M, Lee AG. Tsimchi IM, et al. Ophthalmic Plast Reconstr Surg. 2022 Mar-Apr 01;38(2):e51-e54. doi: 10.1097/IOP.0000000000002095. Ophthalmic Plast Reconstr Surg. 2022. PMID: 35030150
Orbital ependymomas are rare in the orbit and usually occur secondary to extracerebral extension of an intraventricular ependymoma. The authors present a rare case of orbital ependymoma in a 74-year-old female. The patient was initially diagnosed with intrave …
Orbital ependymomas are rare in the orbit and usually occur secondary to extracerebral extension of an intraventricular ependymoma
Ependymoma of the spinal cord with multiple intradural extramedullary ependymomas: The first case report and literature review.
Wang Y, Luo J, Tan Y, Zhang H. Wang Y, et al. Clin Imaging. 2022 Apr;84:159-163. doi: 10.1016/j.clinimag.2021.12.019. Epub 2022 Jan 10. Clin Imaging. 2022. PMID: 35217285 Review.
Ependymomas are the most prevalent intramedullary neoplasms in adults. Few cases have been reported on exophytic intramedullary ependymoma or multiple non-conus, and non-filum intradural extramedullary (IDEM) ependymomas. ...This is the first case of exophyti
Ependymomas are the most prevalent intramedullary neoplasms in adults. Few cases have been reported on exophytic intramedullary ep
Management of Ependymoma in Children, Adolescents and Young Adults.
Thorp N, Gandola L. Thorp N, et al. Clin Oncol (R Coll Radiol). 2019 Mar;31(3):162-170. doi: 10.1016/j.clon.2018.12.001. Epub 2019 Jan 4. Clin Oncol (R Coll Radiol). 2019. PMID: 30616927 Review.
Paediatric ependymomas are rare, malignant tumours arising throughout the central nervous system, but most frequently (in children) the posterior fossa. ...This article reviews clinical aspects of ependymoma management in children and young people....
Paediatric ependymomas are rare, malignant tumours arising throughout the central nervous system, but most frequently (in children) t …
8,673 results