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Familial Pediatric Clear Cell Meningioma With Germline SMARCE1 Mutation in the United States.

作者信息

Navalkele Pournima, Guzman Miguel, Kirby Amelia, Pinz Hailey, Kemp Joanna

机构信息

Department of Pediatrics, Cardinal Glennon Children's Hospital, St. Louis University, St. Louis, Missouri.

Department of Pathology, Cardinal Glennon Children's Hospital, St. University, St. Louis University, St. Louis, Missouri.

出版信息

J Neuropathol Exp Neurol. 2020 Nov 1;79(11):1250-1252. doi: 10.1093/jnen/nlaa115.

Abstract
摘要

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本文引用的文献

1
Hereditary clear cell meningiomas in a single family: three-cases report.
Acta Neurochir (Wien). 2018 Dec;160(12):2321-2325. doi: 10.1007/s00701-018-3727-1. Epub 2018 Nov 13.
2
Familial Syndromes Involving Meningiomas Provide Mechanistic Insight Into Sporadic Disease.
Neurosurgery. 2018 Dec 1;83(6):1107-1118. doi: 10.1093/neuros/nyy121.
4
SMARCE1 mutation screening in classification of clear cell meningiomas.
Histopathology. 2017 Apr;70(5):814-820. doi: 10.1111/his.13135. Epub 2017 Feb 2.
5
A heritable form of SMARCE1-related meningiomas with important implications for follow-up and family screening.
Neurogenetics. 2016 Apr;17(2):83-9. doi: 10.1007/s10048-015-0472-y. Epub 2016 Jan 23.
6
Pediatric intracranial clear cell meningioma associated with a germline mutation of SMARCE1: a novel case.
Childs Nerv Syst. 2015 Mar;31(3):441-7. doi: 10.1007/s00381-014-2558-5. Epub 2014 Sep 24.
7
Germline SMARCE1 mutations predispose to both spinal and cranial clear cell meningiomas.
J Pathol. 2014 Dec;234(4):436-40. doi: 10.1002/path.4427. Epub 2014 Oct 6.
8
Loss-of-function mutations in SMARCE1 cause an inherited disorder of multiple spinal meningiomas.
Nat Genet. 2013 Mar;45(3):295-8. doi: 10.1038/ng.2552. Epub 2013 Feb 3.
9
Intraspinal familial clear cell meningioma in a mother and child. Case report.
J Neurosurg. 2000 Oct;93(2 Suppl):317-21. doi: 10.3171/spi.2000.93.2.0317.

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