Literature DB >> 2300254

Familial meningioma.

J R McDowell1.   

Abstract

A mother and 3 daughters had meningiomas, pathologically confirmed in all but 1 daughter. One of the tumors had mild atypical features, but chromosomal analysis was normal. In 3 of the cases, peripheral chromosomal analysis was normal. There was no evidence of neurofibromatosis.

Entities:  

Mesh：

Year:  1990        PMID： 2300254     DOI： 10.1212/wnl.40.2.312

Source DB:  PubMed          Journal:  Neurology        ISSN： 0028-3878            Impact factor:   9.910


  5 in total

1.  Equal parental origin of chromosome 22 losses in human sporadic meningioma: no evidence for genomic imprinting.

Authors:  B Fontaine; G A Rouleau; B Seizinger; A F Jewell; M P Hanson; R L Martuza; J F Gusella
Journal:  Am J Hum Genet       Date:  1990-11       Impact factor: 11.025

Review 2.  Molecular pathogenesis of meningiomas.

Authors:  Arie Perry; David H Gutmann; Guido Reifenberger
Journal:  J Neurooncol       Date:  2004-11       Impact factor: 4.130

3.  Familial CNS tumors.

Authors:  J P Sieb; S M Pulst; A Buch
Journal:  J Neurol       Date:  1992-07       Impact factor: 4.849

4.  Fabry disease: Four case reports of meningioma and a review of the literature on other malignancies.

Authors:  Beth L Thurberg; Dominique P Germain; Fernando Perretta; Iulia E Jurca-Simina; Juan M Politei
Journal:  Mol Genet Metab Rep       Date:  2016-10-01

5.  Genomic profiling distinguishes familial multiple and sporadic multiple meningiomas.

Authors:  Yiping Shen; Fabio Nunes; Anat Stemmer-Rachamimov; Marianne James; Gayatry Mohapatra; Scott Plotkin; Rebecca A Betensky; David A Engler; Jennifer Roy; Vijaya Ramesh; James F Gusella
Journal:  BMC Med Genomics       Date:  2009-07-09       Impact factor: 3.063
  5 in total

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