Leukodystrophies underlying cryptic spastic paraparesis: frequency and phenotype in 76 patients-Reference-Cited by-同舟云学术

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Leukodystrophies underlying cryptic spastic paraparesis: frequency and phenotype in 76 patients

Published:2014-04-02 Issue:7 Volume:21 Page:983-988
ISSN:1351-5101
Container-title:European Journal of Neurology
language:en
Short-container-title:Eur J Neurol

Author:

Müller vom Hagen J.¹²,Karle K. N.¹²,Schüle R.¹²,Krägeloh-Mann I.²³,Schöls L.¹²

Affiliation:

1. Department of Neurodegenerative Diseases; Hertie-Institute for Clinical Brain Research; University of Tübingen; Tübingen Germany

2. German Centre for Neurodegenerative Diseases (DZNE); Tübingen Germany

3. Department of Neuropediatrics; University of Tübingen; Tübingen Germany

Funder

German Ministry of Education and Research (BMBF)

Publisher

Wiley

Subject

Clinical Neurology,Neurology

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/ene.12423/fullpdf

Reference20 articles.

1. Frequency and phenotype of SPG11 and SPG15 in complicated hereditary spastic paraplegia;Schule;J Neurol Neurosurg Psychiatry,2009

2. Familial adult onset of Krabbe's disease resembling hereditary spastic paraplegia with normal neuroimaging;Bajaj;J Neurol Neurosurg Psychiatry,2002

3. Prevalence of lysosomal storage disorders;Meikle;JAMA,1999

4. Lysosomal storage disorders: diagnostic dilemmas and prospects for therapy;Wenger;Genet Med,2002

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