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

Year Number of Results
2012 3
2013 3
2014 11
2015 9
2016 2
2017 3
2018 2
2019 5
2020 6
2021 3
2022 1
2023 2
2024 0

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41 results

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Page 1
Efficacy of High-Dose Chemotherapy and Three-Dimensional Conformal Radiation for Atypical Teratoid/Rhabdoid Tumor: A Report From the Children's Oncology Group Trial ACNS0333.
Reddy AT, Strother DR, Judkins AR, Burger PC, Pollack IF, Krailo MD, Buxton AB, Williams-Hughes C, Fouladi M, Mahajan A, Merchant TE, Ho B, Mazewski CM, Lewis VA, Gajjar A, Vezina LG, Booth TN, Parsons KW, Poss VL, Zhou T, Biegel JA, Huang A. Reddy AT, et al. J Clin Oncol. 2020 Apr 10;38(11):1175-1185. doi: 10.1200/JCO.19.01776. Epub 2020 Feb 27. J Clin Oncol. 2020. PMID: 32105509 Free PMC article.
PATIENTS AND METHODS: Patients from birth to 22 years of age with AT/RT were eligible. After surgery, they received 2 courses of multiagent chemotherapy, followed by 3 courses of high-dose chemotherapy with peripheral blood stem cell rescue and involved-field radiat …
PATIENTS AND METHODS: Patients from birth to 22 years of age with AT/RT were eligible. After surgery, they received 2 courses of mult …
Embryonal Tumors of the Central Nervous System: An Update.
Blessing MM, Alexandrescu S. Blessing MM, et al. Surg Pathol Clin. 2020 Jun;13(2):235-247. doi: 10.1016/j.path.2020.01.003. Epub 2020 Apr 7. Surg Pathol Clin. 2020. PMID: 32389264 Review.
Well-defined embryonal tumors include medulloblastoma, atypical teratoid/rhabdoid tumor, embryonal tumor with multilayered rosettes, C19MC-altered and embryonal tumor with multilayered rosettes, not otherwise specified, pineoblastoma, pituitary blastoma, CNS neuroblastoma, and ga …
Well-defined embryonal tumors include medulloblastoma, atypical teratoid/rhabdoid tumor, embryonal tumor with multilayered rosettes, C19MC-a …
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.
They are highly cellular tumors with brisk mitotic activity, and they share a propensity for dissemination throughout the neuroaxis. Emerging molecular data enable improved diagnostic and prognostic discrimination for these tumors. Because of their aggressive potential, th …
They are highly cellular tumors with brisk mitotic activity, and they share a propensity for dissemination throughout the neuroaxis. Emergin …
Spinal Atypical Rhabdoid Teratoid Tumor in an Adult Woman: Case Report and Review of the Literature.
Neromyliotis E, Kalyvas AV, Drosos E, Komaitis S, Bartziotas D, Skandalakis GP, Stranjalis G, Koutsarnakis C. Neromyliotis E, et al. World Neurosurg. 2019 Aug;128:196-199. doi: 10.1016/j.wneu.2019.05.007. Epub 2019 May 10. World Neurosurg. 2019. PMID: 31082562 Review.
They are invariantly characterized by multiple relapses and dismal prognosis. The clinician must be attentive of leptomeningeal disseminations and 22q11 deletion-associated comorbidities....
They are invariantly characterized by multiple relapses and dismal prognosis. The clinician must be attentive of leptomeningeal disse …
Screening for genes and subnetworks associated with atypical teratoid/rhabdoid tumors using bioinformatics analysis.
Li G, Wang Y, Cai L, Zhou L. Li G, et al. Int J Neurosci. 2021 Apr;131(4):319-326. doi: 10.1080/00207454.2020.1746306. Epub 2020 Apr 7. Int J Neurosci. 2021. PMID: 32202192
Objectives: Atypical teratoid/rhabdoid tumors (AT/RTs) are rare, fast-growing lesions of central nervous system and their prognosis is poor. Nowadays, multimodal managements, including surgery, chemotherapy and radiation therapy are advocated; however, low survival rate an …
Objectives: Atypical teratoid/rhabdoid tumors (AT/RTs) are rare, fast-growing lesions of central nervous system and their prognosis i …
Recurrent atypical teratoid/rhabdoid tumors (AT/RT) reveal discrete features of progression on histology, epigenetics, copy number profiling, and transcriptomics.
Johann PD, Altendorf L, Efremova EM, Holsten T, Steinbügl M, Nemes K, Eckhardt A, Kresbach C, Bockmayr M, Koch A, Haberler C, Antonelli M, DeSisto J, Schuhmann MU, Hauser P, Siebert R, Bens S, Kool M, Green AL, Hasselblatt M, Frühwald MC, Schüller U. Johann PD, et al. Acta Neuropathol. 2023 Sep;146(3):527-541. doi: 10.1007/s00401-023-02608-7. Epub 2023 Jul 14. Acta Neuropathol. 2023. PMID: 37450044 Free PMC article.
Overall, our work identifies subtle molecular changes that occur in the course of the disease and that may help define novel therapeutic targets for AT/RT recurrences....
Overall, our work identifies subtle molecular changes that occur in the course of the disease and that may help define novel therapeu …
Sellar Atypical Teratoid/Rhabdoid Tumor (AT/RT): A Clinicopathologically and Genetically Distinct Variant of AT/RT.
Nakata S, Nobusawa S, Hirose T, Ito S, Inoshita N, Ichi S, Amatya VJ, Takeshima Y, Sugiyama K, Sonoda Y, Haga H, Hirato J, Nakazato Y, Yokoo H. Nakata S, et al. Am J Surg Pathol. 2017 Jul;41(7):932-940. doi: 10.1097/PAS.0000000000000845. Am J Surg Pathol. 2017. PMID: 28338502
We herein investigated a series of 6 sellar AT/RT for histopathologic features, the molecular status of the INI1/SMARCB1 gene, and clinical courses. All 6 cases were adult females, ranging in age from 21 to 69 years old. ...
We herein investigated a series of 6 sellar AT/RT for histopathologic features, the molecular status of the INI1/SMARCB1 gene, and clinical …
Drug screening with a novel tumor-derived cell line identified alternative therapeutic options for patients with atypical teratoid/rhabdoid tumor.
Nakano Y, Takadera M, Miyazaki M, Qiao Z, Nakajima K, Noguchi R, Oyama R, Kimura Y, Okuhiro Y, Yamasaki K, Kunihiro N, Fukushima H, Inoue T, Hara J, Ozawa T, Kondo T, Ichimura K. Nakano Y, et al. Hum Cell. 2021 Jan;34(1):271-278. doi: 10.1007/s13577-020-00438-3. Epub 2020 Sep 30. Hum Cell. 2021. PMID: 32997328
Atypical teratoid/rhabdoid tumor (AT/RT) is a rare intracranial tumor occurring predominantly in young children. The prognosis is poor, and no effective treatment is currently available. ...
Atypical teratoid/rhabdoid tumor (AT/RT) is a rare intracranial tumor occurring predominantly in young children. The prognosis is poo …
41 results