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Results by year

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

Year Number of Results
1964 1
1965 1
1966 1
1967 6
1968 5
1969 10
1970 12
1971 18
1972 18
1973 13
1974 16
1975 14
1976 17
1977 18
1978 15
1979 15
1980 13
1981 20
1982 8
1983 17
1984 37
1985 46
1986 31
1987 35
1988 39
1989 45
1990 57
1991 85
1992 73
1993 77
1994 93
1995 83
1996 82
1997 91
1998 69
1999 72
2000 94
2001 79
2002 70
2003 110
2004 93
2005 123
2006 74
2007 78
2008 92
2009 105
2010 104
2011 119
2012 128
2013 106
2014 90
2015 103
2016 107
2017 96
2018 122
2019 79
2020 106
2021 116
2022 131
2023 103
2024 12

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Search Results

3,448 results

Results by year

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Page 1
Translocation-related sarcomas.
Mertens F, Antonescu CR, Hohenberger P, Ladanyi M, Modena P, D'Incalci M, Casali PG, Aglietta M, Alvegård T. Mertens F, et al. Semin Oncol. 2009 Aug;36(4):312-23. doi: 10.1053/j.seminoncol.2009.06.004. Semin Oncol. 2009. PMID: 19664492 Review.
Ewing sarcoma.
Choi EY, Gardner JM, Lucas DR, McHugh JB, Patel RM. Choi EY, et al. Semin Diagn Pathol. 2014 Jan;31(1):39-47. doi: 10.1053/j.semdp.2014.01.002. Epub 2014 Jan 5. Semin Diagn Pathol. 2014. PMID: 24680181 Review.
Classification of small round cell tumors of bone is often challenging due to overlapping clinicopathologic features. The purpose of this article is to review the clinical, radiological, histologic, and molecular features of Ewing sarcoma and to provide a discussion of the …
Classification of small round cell tumors of bone is often challenging due to overlapping clinicopathologic features. The purpose of …
Embryonal brain tumors.
McGovern SL, Grosshans D, Mahajan A. McGovern SL, et al. Cancer J. 2014 Nov-Dec;20(6):397-402. doi: 10.1097/PPO.0000000000000081. Cancer J. 2014. PMID: 25415685 Review.
Embryonal brain tumors are a heterogeneous group of neoplasms that primarily occur in infants and young children. ...This review describes the role of radiation in general and proton therapy in particular for the treatment of medulloblastoma, central nervous system prim
Embryonal brain tumors are a heterogeneous group of neoplasms that primarily occur in infants and young children. ...This review desc …
Status of Surveillance and Nonsurgical Therapy for Small Nonfunctioning Pancreatic Neuroendocrine Tumors.
van Beek DJ, Verschuur AVD, Brosens LAA, Valk GD, Pieterman CRC, Vriens MR. van Beek DJ, et al. Surg Oncol Clin N Am. 2023 Apr;32(2):343-371. doi: 10.1016/j.soc.2022.10.010. Surg Oncol Clin N Am. 2023. PMID: 36925190 Review.

Pancreatic neuroendocrine tumors (PNETs) occur in < 1/100,000 patients and most are nonfunctioning (NF). ...Surgery is generally recommended for nonfunctional pancreatic neuroendocrine tumors (NF-PNETs) >2 cm to prevent metastases. For tumors 2 cm, acti

Pancreatic neuroendocrine tumors (PNETs) occur in < 1/100,000 patients and most are nonfunctioning (NF). ...Surgery is generally r

Intraocular medulloepithelioma.
Saunders T, Margo CE. Saunders T, et al. Arch Pathol Lab Med. 2012 Feb;136(2):212-6. doi: 10.5858/arpa.2010-0669-RS. Arch Pathol Lab Med. 2012. PMID: 22288972 Free article. Review.
Esthesioneuroblastoma.
Elkon D, Hightower SI, Lim ML, Cantrell RW, Constable WC. Elkon D, et al. Cancer. 1979 Sep;44(3):1087-94. doi: 10.1002/1097-0142(197909)44:3<1087::aid-cncr2820440343>3.0.co;2-a. Cancer. 1979. PMID: 383268 Review.
ETMR: a tumor entity in its infancy.
Lambo S, von Hoff K, Korshunov A, Pfister SM, Kool M. Lambo S, et al. Acta Neuropathol. 2020 Sep;140(3):249-266. doi: 10.1007/s00401-020-02182-2. Epub 2020 Jun 29. Acta Neuropathol. 2020. PMID: 32601913 Free PMC article. Review.
All ETMRs, despite their highly heterogeneous histology, are characterized by specific high expression of the RNA-binding protein LIN28A, which is, therefore, often used as a diagnostic marker for these tumors. ETMRs have few recurrent genetic aberrations, mainly affecting …
All ETMRs, despite their highly heterogeneous histology, are characterized by specific high expression of the RNA-binding protein LIN28A, wh …
Pediatric Orbital Primitive Neuroectodermal Tumors.
Afghani T, Mansoor H, Raza Hamdani SN. Afghani T, et al. J Pediatr Ophthalmol Strabismus. 2018 Mar 1;55(2):128-134. doi: 10.3928/01913913-20170703-03. Epub 2017 Nov 14. J Pediatr Ophthalmol Strabismus. 2018. PMID: 29131914 Review.
PURPOSE: To present the clinical, radiological, histopathological, immunohistochemical features and the follow-up of orbital primitive neuroectodermal tumors (PNETs) in pediatric patients along with a review of the literature. ...CONCLUSIONS: The authors beli …
PURPOSE: To present the clinical, radiological, histopathological, immunohistochemical features and the follow-up of orbital primitive
[Peripheral neuroblastic tumors in childhood].
Bernhardt M, Vokuhl C. Bernhardt M, et al. Pathologie (Heidelb). 2023 Nov;44(6):366-372. doi: 10.1007/s00292-023-01227-z. Epub 2023 Oct 11. Pathologie (Heidelb). 2023. PMID: 37819531 Review. German.
Peripheral neuroblastic tumors represent the fourth-largest group of malignant tumors in childhood. The majority of these tumors are neuroblastomas, which can be classified into undifferentiated, poorly differentiated, and differentiating subtypes. ...
Peripheral neuroblastic tumors represent the fourth-largest group of malignant tumors in childhood. The majority of these t
3,448 results