Multifocal nerve lesions andLZTR1germline mutations in segmental schwannomatosis-Reference-Cited by-同舟云学术

Multifocal nerve lesions andLZTR1germline mutations in segmental schwannomatosis

Published:2016-08-13 Issue:4 Volume:80 Page:625-628
ISSN:0364-5134
Container-title:Annals of Neurology
language:en
Short-container-title:Ann Neurol.

Author:

Farschtschi Said¹,Mautner Victor-Felix¹,Pham Mirko²,Nguyen Rosa³,Kehrer-Sawatzki Hildegard⁴,Hutter Sonja⁵,Friedrich Reinhard E.⁶,Schulz Alexander⁷,Morrison Helen⁷,Jones David T. W.⁵,Bendszus Martin²,Bäumer Philipp²⁸

Affiliation:

1. Department of Neurology; University Medical Center Hamburg-Eppendorf, University of Hamburg; Hamburg Germany

2. Department of Neuroradiology; Heidelberg University Hospital; Heidelberg Germany

3. Department of Oncology; St Jude Children's Research Hospital; Memphis TN

4. Institute of Human Genetics; University of Ulm; Ulm Germany

5. Division of Pediatric Neuro-oncology; German Cancer Research Center; Heidelberg Germany

6. Department of Maxillofacial Surgery; University Medical Center Hamburg-Eppendorf, University of Hamburg; Hamburg Germany

7. Leibniz Institute on Aging; Fritz Lipmann Institute; Jena Germany

8. Department of Radiology; German Cancer Research Center; Heidelberg Germany

Funder

Märta and Erik Karberg Foundation for Medical Research

Bundesverband Neurofibromatose

Medical Faculty of the University of Heidelberg

Publisher

Wiley

Subject

Neurology (clinical),Neurology

Reference16 articles.

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2. Increasing the specificity of diagnostic criteria for schwannomatosis;Baser;Neurology,2006

3. Update from the 2011 International Schwannomatosis Workshop: From genetics to diagnostic criteria;Plotkin;Am J Med Genet A,2013

4. Frequency of SMARCB1 mutations in familial and sporadic schwannomatosis;Smith;Neurogenetics,2012

5. Germline loss-of-function mutations in LZTR1 predispose to an inherited disorder of multiple schwannomas;Piotrowski;Nat Genet,2014

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