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

Year Number of Results
1922 2
1923 1
1926 2
1927 1
1930 1
1931 1
1932 1
1934 1
1935 2
1936 1
1939 2
1941 1
1945 1
1946 3
1947 10
1948 6
1949 5
1950 10
1951 17
1952 18
1953 20
1954 9
1955 17
1956 17
1957 17
1958 13
1959 17
1960 15
1961 19
1962 13
1963 20
1964 28
1965 19
1966 26
1967 29
1968 24
1969 38
1970 40
1971 35
1972 25
1973 30
1974 32
1975 37
1976 21
1977 39
1978 28
1979 39
1980 36
1981 48
1982 35
1983 51
1984 51
1985 55
1986 64
1987 58
1988 51
1989 65
1990 59
1991 60
1992 61
1993 68
1994 63
1995 74
1996 65
1997 60
1998 61
1999 65
2000 80
2001 92
2002 80
2003 73
2004 78
2005 100
2006 100
2007 119
2008 120
2009 170
2010 161
2011 154
2012 162
2013 183
2014 221
2015 173
2016 221
2017 261
2018 227
2019 239
2020 265
2021 295
2022 265
2023 243
2024 93

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5,570 results

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Page 1
Chordoma.
Ulici V, Hart J. Ulici V, et al. Arch Pathol Lab Med. 2022 Mar 1;146(3):386-395. doi: 10.5858/arpa.2020-0258-RA. Arch Pathol Lab Med. 2022. PMID: 34319396 Free article. Review.
OBJECTIVE.-: To summarize the clinical and pathologic findings of the various types of chordoma (conventional chordoma, dedifferentiated chordoma, and poorly differentiated chordoma), the differential diagnosis, and recent advances in molecular pathoge …
OBJECTIVE.-: To summarize the clinical and pathologic findings of the various types of chordoma (conventional chordoma, dediff …
[Chordoma-An update].
Mellert K, Seeling C, Möller P, Barth TFE. Mellert K, et al. Pathologie (Heidelb). 2022 Aug;43(Suppl 1):50-55. doi: 10.1007/s00292-022-01118-9. Epub 2022 Sep 29. Pathologie (Heidelb). 2022. PMID: 36175666 Review. German.
Chordomas are rare malignant tumors of the axial skeleton with notochordal differentiation. From a morphological point of view, chordomas display a broad spectrum ranging from the classical, conventional form not otherwise specified (NOS) to forms with hepatoid or r
Chordomas are rare malignant tumors of the axial skeleton with notochordal differentiation. From a morphological point of view, ch
[Chordoma: is there a molecular basis for diagnosis and treatment?].
Scheipl S, Igrec J, Leithner A, Smolle M, Haybäck J, Liegl B. Scheipl S, et al. Pathologe. 2020 Mar;41(2):153-162. doi: 10.1007/s00292-020-00761-4. Pathologe. 2020. PMID: 32100085 Review. German.
Chordomas are malignant bone tumours with a reported annual incidence of 0.08 per 100,000 cases. ...Brachyury seems to play a key role in the pathogenesis of chordoma, though the detailed mechanism still needs to be elucidated. ...
Chordomas are malignant bone tumours with a reported annual incidence of 0.08 per 100,000 cases. ...Brachyury seems to play a key rol
Chordoma: the entity.
Yakkioui Y, van Overbeeke JJ, Santegoeds R, van Engeland M, Temel Y. Yakkioui Y, et al. Biochim Biophys Acta. 2014 Dec;1846(2):655-69. doi: 10.1016/j.bbcan.2014.07.012. Epub 2014 Sep 3. Biochim Biophys Acta. 2014. PMID: 25193090 Review.
Chordomas are malignant tumors of the axial skeleton, characterized by their locally invasive and slow but aggressive growth. ...Surgical resection with adjuvant radiotherapy is the first-choice treatment modality in these patients, since chordomas are resistant to
Chordomas are malignant tumors of the axial skeleton, characterized by their locally invasive and slow but aggressive growth. ...Surg
Poorly differentiated chordoma: review of 53 cases.
Yeter HG, Kosemehmetoglu K, Soylemezoglu F. Yeter HG, et al. APMIS. 2019 Sep;127(9):607-615. doi: 10.1111/apm.12978. APMIS. 2019. PMID: 31243811 Review.
Poorly differentiated chordoma (PDC) is a newly described variant of chordomas, which is not considered as a subtype yet, but has its own distinct features in terms of morphology, immunohistochemical and molecular characteristics, and clinical outcome. To provide a …
Poorly differentiated chordoma (PDC) is a newly described variant of chordomas, which is not considered as a subtype yet, but …
[Chordoma].
George B, Bresson D, Bouazza S, Froelich S, Mandonnet E, Hamdi S, Orabi M, Polivka M, Cazorla A, Adle-Biassette H, Guichard JP, Duet M, Gayat E, Vallée F, Canova CH, Riet F, Bolle S, Calugaru V, Dendale R, Mazeron JJ, Feuvret L, Boissier E, Vignot S, Puget S, Sainte-Rose C, Beccaria K. George B, et al. Neurochirurgie. 2014 Jun;60(3):63-140. doi: 10.1016/j.neuchi.2014.02.003. Epub 2014 May 23. Neurochirurgie. 2014. PMID: 24856008 Review. French.
PURPOSES: To review in the literature, all the epidemiological, clinical, radiological, histological and therapeutic data regarding chordomas as well as various notochordal entities: ecchordosis physaliphora, intradural and intraparenchymatous chordomas, benign noto …
PURPOSES: To review in the literature, all the epidemiological, clinical, radiological, histological and therapeutic data regarding chord
Chordoma: radiological-pathological correlation.
Maclean FM, Soo MY, Ng T. Maclean FM, et al. Australas Radiol. 2005 Aug;49(4):261-8. doi: 10.1111/j.1440-1673.2005.01433.x. Australas Radiol. 2005. PMID: 16026431 Review.
This review correlates the imaging findings and histological appearances seen in chordomas in a series of patients presenting at our institution, together with a published literature review. ...
This review correlates the imaging findings and histological appearances seen in chordomas in a series of patients presenting at our …
Chordoma metastatic to skin: A report of two cases and a brief review of the literature.
Dimopoulos YP, Ivan D, Prieto VG, Aung PP. Dimopoulos YP, et al. J Cutan Pathol. 2023 Jun;50(6):500-504. doi: 10.1111/cup.14348. Epub 2022 Nov 23. J Cutan Pathol. 2023. PMID: 36349402 Review.
In the first case, a patient with a primary thoracic/lumbar chordoma presented with isolated metastasis to the skin of the left lower jaw 9 years after initial diagnosis of the chordoma. To our knowledge, this is the first reported case of a chordoma of this …
In the first case, a patient with a primary thoracic/lumbar chordoma presented with isolated metastasis to the skin of the left lower …
Personalized chordoma organoids for drug discovery studies.
Al Shihabi A, Davarifar A, Nguyen HTL, Tavanaie N, Nelson SD, Yanagawa J, Federman N, Bernthal N, Hornicek F, Soragni A. Al Shihabi A, et al. Sci Adv. 2022 Feb 18;8(7):eabl3674. doi: 10.1126/sciadv.abl3674. Epub 2022 Feb 16. Sci Adv. 2022. PMID: 35171675 Free PMC article.
Chordomas are rare tumors of notochordal origin, most commonly arising in the sacrum or skull base. Chordomas are considered insensitive to conventional chemotherapy, and their rarity complicates running timely and adequately powered trials to identify effective tre
Chordomas are rare tumors of notochordal origin, most commonly arising in the sacrum or skull base. Chordomas are considered i
[Chordoma as a neurosurgical pathology].
Sidorin VS, Efimov AV, Strelkina KA, Sokolova TV, Orlov AY, Zabrodskaya YM. Sidorin VS, et al. Arkh Patol. 2022;84(3):24-31. doi: 10.17116/patol20228403124. Arkh Patol. 2022. PMID: 35639840 Russian.
MATERIAL AND METHODS: An analysis of 28 chordomas was carried out. All chordomas were histologically verified, including using immunohistochemical markers of notochordal differentiation (S100, EMA, keratin, brachiuria protein). ...According to histopathological crit …
MATERIAL AND METHODS: An analysis of 28 chordomas was carried out. All chordomas were histologically verified, including using …
5,570 results