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
1990 1
1992 1
1993 1
1995 2
1997 1
1999 1
2001 1
2002 1
2004 2
2011 1
2012 2
2013 1
2015 1
2024 0

Text availability

Article attribute

Article type

Publication date

Search Results

16 results

Results by year

Filters applied: . Clear all
Quoted phrase not found in phrase index: "Deletion of Chromosome 22 Associated Meningioma"
Page 1
Meningiomas.
Black PM. Black PM. Neurosurgery. 1993 Apr;32(4):643-57. doi: 10.1227/00006123-199304000-00023. Neurosurgery. 1993. PMID: 8474655 Review.
Factors predisposing to meningioma formation include female sex, previous ionizing radiation, and Type 2 neurofibromatosis. The first factor may act through the expression of sex hormone receptors, especially the progesterone receptor, in these tumors; the other two probab …
Factors predisposing to meningioma formation include female sex, previous ionizing radiation, and Type 2 neurofibromatosis. The first …
Neurofibromatosis type 2.
Evans GR, Lloyd SKW, Ramsden RT. Evans GR, et al. Adv Otorhinolaryngol. 2011;70:91-98. doi: 10.1159/000322482. Epub 2011 Feb 24. Adv Otorhinolaryngol. 2011. PMID: 21358190 Review.
Neurofibromatosis type 2 (NF2) is an autosomal-dominant inherited tumour predisposition syndrome caused by mutations in the NF2 gene on chromosome 22. Affected individuals develop schwannomas characteristically affecting both vestibular nerves leading to hear …
Neurofibromatosis type 2 (NF2) is an autosomal-dominant inherited tumour predisposition syndrome caused by mutations in the NF2 gene …
Neurofibromatosis type 2 (NF2): diagnosis and management.
Lloyd SK, Evans DG. Lloyd SK, et al. Handb Clin Neurol. 2013;115:957-67. doi: 10.1016/B978-0-444-52902-2.00054-0. Handb Clin Neurol. 2013. PMID: 23931824 Review.
Neurofibromatosis type 2 (NF2) is an autosomal dominant inherited tumor predisposition syndrome caused by mutations in the NF2 gene on chromosome 22. Affected individuals develop schwannomas typically involving both vestibular nerves leading to hearing loss a …
Neurofibromatosis type 2 (NF2) is an autosomal dominant inherited tumor predisposition syndrome caused by mutations in the NF2 gene o …
Meningioma in Down Syndrome.
Yamamoto T, Shinojima N, Todaka T, Nishikawa S, Yano S, Kuratsu J. Yamamoto T, et al. World Neurosurg. 2015 Sep;84(3):866.e1-6. doi: 10.1016/j.wneu.2015.03.065. Epub 2015 Apr 9. World Neurosurg. 2015. PMID: 25862935
Postoperatively, the patient's neurologic status improved, and there was no tumor regrowth in the next 2 years. Fluorescence in situ hybridization for chromosome 22 confirmed high allele loss involving the neurofibromin 2 gene locus, a finding typical in m …
Postoperatively, the patient's neurologic status improved, and there was no tumor regrowth in the next 2 years. Fluorescence in situ hybridi …
Radiation-associated meningiomas in children: clinical, pathological, and cytogenetic characteristics with a critical review of the literature.
Elbabaa SK, Gokden M, Crawford JR, Kesari S, Saad AG. Elbabaa SK, et al. J Neurosurg Pediatr. 2012 Oct;10(4):281-90. doi: 10.3171/2012.7.PEDS1251. Epub 2012 Aug 17. J Neurosurg Pediatr. 2012. PMID: 22900483 Review.
OBJECT: Radiation-associated meningiomas (RAMs) arise after treatment with radiation to the cranium and are recognized as clinically separate from sporadic meningiomas. ...The MIB-1 labeling index was a median of 6.6% (range 4%-10%). Five patients (55.6%) dis …
OBJECT: Radiation-associated meningiomas (RAMs) arise after treatment with radiation to the cranium and are recognized as clin …
Cytogenetics and molecular genetics of nervous system tumors.
Rey JA, Pestaña A, Bello MJ. Rey JA, et al. Oncol Res. 1992;4(8-9):321-31. Oncol Res. 1992. PMID: 1336685 Review.
The available data on meningiomas and neurinomas show that loss of regions on chromosome 22 is the main characteristic feature. Thus, tumor suppressor genes located in this chromosome are non-randomly involved in both neoplasms, and may present as solitary, s …
The available data on meningiomas and neurinomas show that loss of regions on chromosome 22 is the main characteristic …
Loss of heterozygosity analysis of benign, atypical, and anaplastic meningiomas.
Lee JY, Finkelstein S, Hamilton RL, Rekha R, King JT Jr, Omalu B. Lee JY, et al. Neurosurgery. 2004 Nov;55(5):1163-73. doi: 10.1227/01.neu.0000141081.07086.a0. Neurosurgery. 2004. PMID: 15509323
OBJECTIVE: Up to 70% of typical meningiomas demonstrate allelic loss at chromosome 22q. Allelic loss at additional chromosomal loci is associated with atypia and anaplasia in meningiomas. ...This study confirms previously reported chromosomal regions of allel …
OBJECTIVE: Up to 70% of typical meningiomas demonstrate allelic loss at chromosome 22q. Allelic loss at additional chromosomal loci i …
Microdeletion del(22)(q12.2) encompassing the facial development-associated gene, MN1 (meningioma 1) in a child with Pierre-Robin sequence (including cleft palate) and neurofibromatosis 2 (NF2): a case report and review of the literature.
Davidson TB, Sanchez-Lara PA, Randolph LM, Krieger MD, Wu SQ, Panigrahy A, Shimada H, Erdreich-Epstein A. Davidson TB, et al. BMC Med Genet. 2012 Mar 22;13:19. doi: 10.1186/1471-2350-13-19. BMC Med Genet. 2012. PMID: 22436304 Free PMC article. Review.
High resolution karyotype revealed 46, XX, del(22)(q12.1q12.3), FISH confirmed a deletion encompassing NF2, and chromosomal microarray identified a 3,693 kb deletion encompassing multiple genes including NF2 and MN1 (meningioma 1).Five additional patients wit …
High resolution karyotype revealed 46, XX, del(22)(q12.1q12.3), FISH confirmed a deletion encompassing NF2, and chromosomal microarra …
Triple approach for diagnosis and grading of meningiomas: histology, morphometry of Ki-67/Feulgen stainings, and cytogenetics.
Kolles H, Niedermayer I, Schmitt C, Henn W, Feld R, Steudel WI, Zang KD, Feiden W. Kolles H, et al. Acta Neurochir (Wien). 1995;137(3-4):174-81. doi: 10.1007/BF02187190. Acta Neurochir (Wien). 1995. PMID: 8789658
"Atypical" and anaplastic meningiomas recurred in 29% and 50%, respectively. Since the term "atypical" meningioma is confusing in the context of tumour grading, the term "intermediate type meningioma" is proposed. Furthermore, the results of cytogenetic analy …
"Atypical" and anaplastic meningiomas recurred in 29% and 50%, respectively. Since the term "atypical" meningioma is confusing …
Genetics of pediatric central nervous system tumors.
Biegel JA. Biegel JA. J Pediatr Hematol Oncol. 1997 Nov-Dec;19(6):492-501. doi: 10.1097/00043426-199711000-00002. J Pediatr Hematol Oncol. 1997. PMID: 9407934 Review.
A tumor suppressor gene in chromosome band 22q11.2 has been hypothesized to play a role in atypical teratoid/rhabdoid tumors, and positional cloning strategies are in progress to identify a rhabdoid tumor gene. Chromosome 22 deletions are also s …
A tumor suppressor gene in chromosome band 22q11.2 has been hypothesized to play a role in atypical teratoid/rhabdoid tumors, and pos …
16 results