Literature DB >> 3927391

Central neurofibromatosis.

S M Huson, D C Thrush.   

Abstract

The clinical details and autopsy studies of six members from two generations of a family with central neurofibromatosis are reviewed. Five of the six had other tumours of the central nervous system. The problems of management are discussed and a programme for screening at-risk relatives proposed.

Entities:  

Mesh：

Year:  1985        PMID： 3927391

Source DB:  PubMed          Journal:  Q J Med        ISSN： 0033-5622


  4 in total

1.  A genetic study of type 2 neurofibromatosis in the United Kingdom. I. Prevalence, mutation rate, fitness, and confirmation of maternal transmission effect on severity.

Authors:  D G Evans; S M Huson; D Donnai; W Neary; V Blair; D Teare; V Newton; T Strachan; R Ramsden; R Harris
Journal:  J Med Genet       Date:  1992-12       Impact factor: 6.318

2.  The different forms of neurofibromatosis.

Authors:  S M Huson
Journal:  Br Med J (Clin Res Ed)       Date:  1987-05-02

3.  Molecular genetic approach to human meningioma: loss of genes on chromosome 22.

Authors:  B R Seizinger; S de la Monte; L Atkins; J F Gusella; R L Martuza
Journal:  Proc Natl Acad Sci U S A       Date:  1987-08       Impact factor: 11.205

4.  Mosaicism in neurofibromatosis type 2: an update of risk based on uni/bilaterality of vestibular schwannoma at presentation and sensitive mutation analysis including multiple ligation-dependent probe amplification.

Authors:  D Gareth R Evans; R T Ramsden; A Shenton; C Gokhale; N L Bowers; S M Huson; G Pichert; A Wallace
Journal:  J Med Genet       Date:  2007-02-16       Impact factor: 6.318
  4 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.