Autosomal recessive hereditary spastic paraparesis with thin corpus callosum; report of two sisters
Author:
Publisher
Elsevier BV
Subject
Physiology (medical),Neurology (clinical),Neurology,General Medicine,Surgery
Reference19 articles.
1. Classification of the hereditary ataxias and paraplegias;Harding;Lancet,1983
2. Clinical heterogeneity of autosomal spastic paraparesis: analysis of 106 patients in 46 families;Coutinho;Arch. Neurol.,1999
3. Hereditary spastic paraplegia: the pace quickens;Fink;Ann. Neurol.,2002
4. Linkage of `pure' autosomal recessive familial spastic paraplegia to chromosome 8 markers and evidence of genetic locus heterogeneity;Hentati;Hum. Mol. Genet.,1994
5. Spastic paraplegia and OXPHOS impairment caused by mutations in paraplegin, a nuclear-encoded mitochondrial metalloprotease;Casari;Cell,1998
Cited by 4 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. Microstructural Integrity of Cerebral Fiber Tracts in Hereditary Spastic Paraparesis withSPG11Mutation;American Journal of Neuroradiology;2012-12-06
2. A novel hereditary spastic paraplegia with dystonia linked to chromosome 2q24-2q31;Movement Disorders;2008-11-12
3. Chapter 19 Recessive Spastic Paraplegias;Spinocerebellar Degenerations: The Ataxias and Spastic Paraplegias;2007
4. Thin corpus callosum and amyotrophy in spastic paraplegia—Case report and review of literature;Clinical Neurology and Neurosurgery;2006-10
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