SPG2 mimicking multiple sclerosis in a family identified using next generation sequencing-Reference-Cited by-同舟云学术

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SPG2 mimicking multiple sclerosis in a family identified using next generation sequencing

Published:2017-04 Issue: Volume:375 Page:198-202
ISSN:0022-510X
Container-title:Journal of the Neurological Sciences
language:en
Short-container-title:Journal of the Neurological Sciences

Author:

Rubegni Anna,Battisti Carla,Tessa Alessandra,Cerase Alfonso,Doccini Stefano,Malandrini Alessandro,Santorelli Filippo M.,Federico Antonio

Publisher

Elsevier BV

Subject

Clinical Neurology,Neurology

Reference15 articles.

1. Primary-progressive multiple sclerosis;Miller;Lancet Neurol.,2007

2. From genetic associations to functional studies in multiple sclerosis;Bos;Eur. J. Neurol.,2016

3. Differential diagnosis of Mendelian and mitochondrial disorders in patients with suspected multiple sclerosis;Weisfeld-Adams;Brain,2015

4. Diagnostic criteria for multiple sclerosis: 2010 revisions to the McDonald criteria;Polman;Ann. Neurol.,2011

5. Atypical hereditary spastic paraplegia mimicking multiple sclerosis associated with a novel SPG11 mutation;Romagnolo;Eur. J. Neurol.,2014

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