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
1983 2
1987 2
1988 4
1989 1
1990 2
1991 4
1992 6
1993 6
1994 2
1995 5
1996 8
1997 11
1998 11
1999 13
2000 4
2001 8
2002 5
2003 10
2004 9
2005 11
2006 7
2007 15
2008 14
2009 16
2010 19
2011 21
2012 20
2013 16
2014 28
2015 35
2016 23
2017 19
2018 25
2019 32
2020 40
2021 43
2022 26
2023 28

Text availability

Article attribute

Article type

Publication date

Search Results

483 results

Results by year

Filters applied: . Clear all
Page 1
Pediatric Brain Tumors.
Udaka YT, Packer RJ. Udaka YT, et al. Neurol Clin. 2018 Aug;36(3):533-556. doi: 10.1016/j.ncl.2018.04.009. Neurol Clin. 2018. PMID: 30072070 Review.
Pediatric central nervous system (CNS) tumors are the most common solid tumors in children and comprise 15% to 20% of all malignancies in children. Presentation, symptoms, and signs depend on tumor location and age of the patient at the time of diagnosis. This article summ …
Pediatric central nervous system (CNS) tumors are the most common solid tumors in children and comprise 15% to 20% of all malignancies in ch …
Recent updates in thoracic SMARCA4-deficient undifferentiated tumor.
Nambirajan A, Jain D. Nambirajan A, et al. Semin Diagn Pathol. 2021 Sep;38(5):83-89. doi: 10.1053/j.semdp.2021.06.001. Epub 2021 Jun 4. Semin Diagn Pathol. 2021. PMID: 34147303 Review.
Germline inactivating mutations in SMARCA4 (SWI/SNF-related, matrix-associated, actin-dependent regulator of chromatin, subfamily A, member 4) gene encoding for BRG1 (Brahma related gene-1) are the molecular drivers in small cell carcinoma of ovary, hypercalcemic type (SCCOHT) an …
Germline inactivating mutations in SMARCA4 (SWI/SNF-related, matrix-associated, actin-dependent regulator of chromatin, subfamily A, member …
SMARCA4: Implications of an Altered Chromatin-Remodeling Gene for Cancer Development and Therapy.
Mardinian K, Adashek JJ, Botta GP, Kato S, Kurzrock R. Mardinian K, et al. Mol Cancer Ther. 2021 Dec;20(12):2341-2351. doi: 10.1158/1535-7163.MCT-21-0433. Epub 2021 Oct 12. Mol Cancer Ther. 2021. PMID: 34642211 Free PMC article. Review.
Germline variants in the SMARCA4 gene lead to various hereditary conditions: rhabdoid tumor predisposition syndrome-2 (RTPS2), characterized by loss-of-function alterations and aggressive rhabdoid tumors presenting in infants and young children; and Coffin-Si …
Germline variants in the SMARCA4 gene lead to various hereditary conditions: rhabdoid tumor predisposition syndrome-2 (RTPS2), …
The 2007 WHO classification of tumours of the central nervous system.
Louis DN, Ohgaki H, Wiestler OD, Cavenee WK, Burger PC, Jouvet A, Scheithauer BW, Kleihues P. Louis DN, et al. Acta Neuropathol. 2007 Aug;114(2):97-109. doi: 10.1007/s00401-007-0243-4. Epub 2007 Jul 6. Acta Neuropathol. 2007. PMID: 17618441 Free PMC article. Review.
The fourth edition of the World Health Organization (WHO) classification of tumours of the central nervous system, published in 2007, lists several new entities, including angiocentric glioma, papillary glioneuronal tumour, rosette-forming glioneuronal tumour of the …
The fourth edition of the World Health Organization (WHO) classification of tumours of the central nervous system, published in 2007, lists …
Molecular pathology of tumors of the central nervous system.
Kristensen BW, Priesterbach-Ackley LP, Petersen JK, Wesseling P. Kristensen BW, et al. Ann Oncol. 2019 Aug 1;30(8):1265-1278. doi: 10.1093/annonc/mdz164. Ann Oncol. 2019. PMID: 31124566 Free PMC article. Review.
Molecular characteristics are also important for the diagnosis of several other CNS tumors, such as RELA fusion-positive subtype of ependymoma, atypical teratoid rhabdoid tumor (AT/RT), embryonal tumor with multilayered rosettes, and solitary fibrous tumor …
Molecular characteristics are also important for the diagnosis of several other CNS tumors, such as RELA fusion-positive subtype of ependymo …
SWI/SNF complex-deficient soft tissue neoplasms: An update.
Schaefer IM, Hornick JL. Schaefer IM, et al. Semin Diagn Pathol. 2021 May;38(3):222-231. doi: 10.1053/j.semdp.2020.05.005. Epub 2020 Jun 5. Semin Diagn Pathol. 2021. PMID: 32646614 Free PMC article. Review.
The mammalian SWI/SNF complex consists of 15 subunits encoded by 29 genes, some of which are recurrently mutated in human cancers, in the germline or sporadic setting. Most SWI/SNF-deficient tumors share common "rhabdoid" cytomorphology. SMARCB1 (INI1) is the subunit most …
The mammalian SWI/SNF complex consists of 15 subunits encoded by 29 genes, some of which are recurrently mutated in human cancers, in the ge …
Malignant meningiomas.
Fountain DM, Young AMH, Santarius T. Fountain DM, et al. Handb Clin Neurol. 2020;170:245-250. doi: 10.1016/B978-0-12-822198-3.00044-6. Handb Clin Neurol. 2020. PMID: 32586496 Review.
Malignant meningiomas are WHO Grade III meningiomas representing 1% of all meningiomas. They are comprised of three histologic types: anaplastic, rhabdoid, and papillary. They can arise de novo or as a result of biologic progression of meningiomas of lower histologic grade …
Malignant meningiomas are WHO Grade III meningiomas representing 1% of all meningiomas. They are comprised of three histologic types: anapla …
Renal Medullary Carcinoma.
Elliott A, Bruner E. Elliott A, et al. Arch Pathol Lab Med. 2019 Dec;143(12):1556-1561. doi: 10.5858/arpa.2017-0492-RS. Epub 2019 Mar 11. Arch Pathol Lab Med. 2019. PMID: 30855171 Free article. Review.
Most patients have metastatic disease at the time of presentation. The tumor is characteristically a poorly circumscribed mass in the medullary region, commonly showing variable amounts of hemorrhage and necrosis. Microscopically, a characteristic reticular or cribriform p …
Most patients have metastatic disease at the time of presentation. The tumor is characteristically a poorly circumscribed mass in the …
Lateral Ventricle Atypical Teratoid/Rhabdoid Tumor (AT/RT): Case Report and Review of Literature.
Sharma A, Sable MN, Singla R, Dash C, Sahu RN. Sharma A, et al. Neurol India. 2020 Nov-Dec;68(6):1465-1468. doi: 10.4103/0028-3886.304127. Neurol India. 2020. PMID: 33342894 Review.
Craniotomy and gross total excision of the tumor was achieved. Histopathological examination was suggestive of Atypical Teratoid/Rhabdoid tumor. ...Differential diagnosis of AT/RT must be kept in cases of lateral ventricle tumor in pediatric population …
Craniotomy and gross total excision of the tumor was achieved. Histopathological examination was suggestive of Atypical Teratoid/R …
The International Society of Urological Pathology (ISUP) grading system for renal cell carcinoma and other prognostic parameters.
Delahunt B, Cheville JC, Martignoni G, Humphrey PA, Magi-Galluzzi C, McKenney J, Egevad L, Algaba F, Moch H, Grignon DJ, Montironi R, Srigley JR; Members of the ISUP Renal Tumor Panel. Delahunt B, et al. Am J Surg Pathol. 2013 Oct;37(10):1490-504. doi: 10.1097/PAS.0b013e318299f0fb. Am J Surg Pathol. 2013. PMID: 24025520
Issues relating to prognostic factors were coordinated by a workgroup who identified tumor morphotype, sarcomatoid/rhabdoid differentiation, tumor necrosis, grading, and microvascular invasion as potential prognostic parameters. ...Tumor necrosis was c …
Issues relating to prognostic factors were coordinated by a workgroup who identified tumor morphotype, sarcomatoid/rhabdoid di …
483 results