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Quoted phrase not found in phrase index: "Childhood Grade 2 Meningioma"
Page 1
Cancer and Central Nervous System Tumor Surveillance in Pediatric Neurofibromatosis 2 and Related Disorders.
Evans DGR, Salvador H, Chang VY, Erez A, Voss SD, Druker H, Scott HS, Tabori U. Evans DGR, et al. Clin Cancer Res. 2017 Jun 15;23(12):e54-e61. doi: 10.1158/1078-0432.CCR-17-0590. Clin Cancer Res. 2017. PMID: 28620005 Review.
The last 26 years have seen a great improvement in understanding of the clinical and molecular features of these conditions as well as insights into management. Childhood presentation of NF2 (often with meningioma) in particular predicts a severe multitumor d …
The last 26 years have seen a great improvement in understanding of the clinical and molecular features of these conditions as well as insig …
Pediatric meningiomas: a single-center experience with 15 consecutive cases and review of the literature.
Santos MV, Furlanetti L, Valera ET, Brassesco MS, Tone LG, de Oliveira RS. Santos MV, et al. Childs Nerv Syst. 2012 Nov;28(11):1887-96. doi: 10.1007/s00381-012-1823-8. Epub 2012 Jun 6. Childs Nerv Syst. 2012. PMID: 22669518 Review.
Six children presented with radiation-induced (RT) meningiomas and five had evidence of neurofibromatosis type 2 (NF2). Three patients had multiple meningiomas (all of them had NF2). Simpson's grade I excision was achieved in 12 out of 15 (80 %). ...
Six children presented with radiation-induced (RT) meningiomas and five had evidence of neurofibromatosis type 2 (NF2). Three …
Clinical features and treatment of World Health Organization grade II and III meningiomas in childhood: report of 23 cases.
Wang XQ, Jiang CC, Zhao L, Gong Y, Hu J, Chen H. Wang XQ, et al. J Neurosurg Pediatr. 2012 Nov;10(5):423-33. doi: 10.3171/2012.7.PEDS12179. Epub 2012 Aug 31. J Neurosurg Pediatr. 2012. PMID: 22938082
OBJECT: High-grade meningiomas in childhood are rare, and their clinical features are unknown. The objective of this study was to determine the clinical characteristics and prognosis of childhood high-grade meningiomas. METHODS: Twenty-th …
OBJECT: High-grade meningiomas in childhood are rare, and their clinical features are unknown. The objective of this st …
Childhood and adolescent meningiomas: a report of 38 cases and review of literature.
Menon G, Nair S, Sudhir J, Rao BR, Mathew A, Bahuleyan B. Menon G, et al. Acta Neurochir (Wien). 2009 Mar;151(3):239-44; discussion 244. doi: 10.1007/s00701-009-0206-8. Epub 2009 Feb 24. Acta Neurochir (Wien). 2009. PMID: 19238320
On histopathology, thirty (73.2%) were grade I, nine (21.9%) were grade II and two (4.9%) were grade III meningiomas. ...CONCLUSION: Childhood meningiomas are uncommon but not rare lesions with a marginal male predominance. ...
On histopathology, thirty (73.2%) were grade I, nine (21.9%) were grade II and two (4.9%) were grade III meni
Immunohistochemical expression of the estrogen receptor-related antigen (ER-D5) in human intracranial tumors.
Khalid H, Yasunaga A, Kishikawa M, Shibata S. Khalid H, et al. Cancer. 1995 May 15;75(10):2571-8. doi: 10.1002/1097-0142(19950515)75:10<2571::aid-cncr2820751026>3.0.co;2-u. Cancer. 1995. PMID: 7736403
RESULTS: Eighty-eight (62%) of the 143 brain tumors showed positive ER-D5 immunoreactivity. ER-D5 expression was observed in 9/30 low grade astrocytomas, in 6/13 anaplastic astrocytomas, in 16/27 glioblastomas, in 2/5 ependymomas, in 5/8 medulloblastomas, in …
RESULTS: Eighty-eight (62%) of the 143 brain tumors showed positive ER-D5 immunoreactivity. ER-D5 expression was observed in 9/30 low …
Late toxicity following craniospinal radiation for early-stage medulloblastoma.
Christopherson KM, Rotondo RL, Bradley JA, Pincus DW, Wynn TT, Fort JA, Morris CG, Mendenhall NP, Marcus RB Jr, Indelicato DJ. Christopherson KM, et al. Acta Oncol. 2014 Apr;53(4):471-80. doi: 10.3109/0284186X.2013.862596. Epub 2014 Feb 24. Acta Oncol. 2014. PMID: 24564687 Clinical Trial.
Four patients developed secondary (non-skin) malignancies, including three meningiomas, one rhabdomyosarcoma, and one glioblastoma multiforme. ...CONCLUSION: Ongoing institutional and cooperative group efforts to minimize radiation exposure are justified given the high rat …
Four patients developed secondary (non-skin) malignancies, including three meningiomas, one rhabdomyosarcoma, and one glioblastoma mu …
Mutations of the p53 tumor suppressor gene in neoplasms of the human nervous system.
Ohgaki H, Eibl RH, Schwab M, Reichel MB, Mariani L, Gehring M, Petersen I, Höll T, Wiestler OD, Kleihues P. Ohgaki H, et al. Mol Carcinog. 1993;8(2):74-80. doi: 10.1002/mc.2940080203. Mol Carcinog. 1993. PMID: 8397797
Mutations leading to an amino acid change were found in three of 11 (27%) low-grade (World Health Organization (WHO) Grade II) astrocytomas. They were located in codon 183 (TCA-->TGA) of exon 5, codon 237 (ATG-->ATA) of exon 7, and codon 273 (CGT-->CAT) of …
Mutations leading to an amino acid change were found in three of 11 (27%) low-grade (World Health Organization (WHO) Grade II) …
Cumulative incidence of secondary neoplasms as a first event after childhood acute lymphoblastic leukemia.
Hijiya N, Hudson MM, Lensing S, Zacher M, Onciu M, Behm FG, Razzouk BI, Ribeiro RC, Rubnitz JE, Sandlund JT, Rivera GK, Evans WE, Relling MV, Pui CH. Hijiya N, et al. JAMA. 2007 Mar 21;297(11):1207-15. doi: 10.1001/jama.297.11.1207. JAMA. 2007. PMID: 17374815
DESIGN, SETTING, AND PATIENTS: Retrospective study of 2169 patients with acute lymphoblastic leukemia treated between 1962 and 1998 at St Jude Children's Research Hospital, Memphis, Tenn, who achieved complete remission and had a median follow-up time of 18.7 years (range, 2
DESIGN, SETTING, AND PATIENTS: Retrospective study of 2169 patients with acute lymphoblastic leukemia treated between 1962 and 1998 at St Ju …
Clinico-morphological pattern of intracranial tumors in children.
Shah SH, Soomro IN, Hussainy AS, Hassan SH. Shah SH, et al. J Pak Med Assoc. 1999 Mar;49(3):63-5. J Pak Med Assoc. 1999. PMID: 10531783
RESULTS: During the study period, fifty-four cases of intracranial tumors were diagnosed in children. The age ranged from 1-1/2 years to 4 years with male to female ratio of 1.1:1. Astrocytoma comprised 39% of all intracranial tumors of childhood. ...Posterior crani …
RESULTS: During the study period, fifty-four cases of intracranial tumors were diagnosed in children. The age ranged from 1-1/2 years …