Literature DB >> 25192507

Hereditary spastic paraplegia: clinical principles and genetic advances.

John K Fink1.   

Abstract

Hereditary spastic paraplegia (HSP) refers to inherited disorders in which spastic gait is either the only feature or is a major syndrome feature. There are more than 70 genetic types of HSP. Neuropathological studies, albeit limited to only a few genetic types of HSP, have identified axon degeneration involving the distal ends of the corticospinal tracts and fasciculus gracilis fibers. In this review, the author highlights the clinical and genetic features of HSP. Thieme Medical Publishers 333 Seventh Avenue, New York, NY 10001, USA.

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Year:  2014        PMID: 25192507     DOI: 10.1055/s-0034-1386767

Source DB:  PubMed          Journal:  Semin Neurol        ISSN: 0271-8235            Impact factor:   3.420


  30 in total

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6.  Transverse endoplasmic reticulum expansion in hereditary spastic paraplegia corticospinal axons.

Authors:  Peng-Peng Zhu; Hui-Fang Hung; Natalia Batchenkova; Jonathon Nixon-Abell; James Henderson; Pengli Zheng; Benoit Renvoisé; Song Pang; C Shan Xu; Stephan Saalfeld; Jan Funke; Yuxiang Xie; Fabian Svara; Harald F Hess; Craig Blackstone
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7.  A series of Greek children with pure hereditary spastic paraplegia: clinical features and genetic findings.

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8.  CYP2U1 mutations in two Iranian patients with activity induced dystonia, motor regression and spastic paraplegia.

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Review 9.  Expanding the clinical relevance of the 5'-nucleotidase cN-II/NT5C2.

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