Literature DB >> 4097834

Hereditary spastic paraparesis with sensory neuropathy.

R H Koenig, A J Spiro.   

Abstract

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Year:  1970        PMID： 4097834     DOI： 10.1111/j.1469-8749.1970.tb01965.x

Source DB:  PubMed          Journal:  Dev Med Child Neurol        ISSN： 0012-1622            Impact factor:   5.449


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  5 in total

Review 1.  Hereditary spastic paraparesis: a review of new developments.

Authors:  C McDermott; K White; K Bushby; P Shaw
Journal:  J Neurol Neurosurg Psychiatry       Date:  2000-08       Impact factor: 10.154

2.  Mutation in the epsilon subunit of the cytosolic chaperonin-containing t-complex peptide-1 (Cct5) gene causes autosomal recessive mutilating sensory neuropathy with spastic paraplegia.

Authors:  A Bouhouche; A Benomar; N Bouslam; T Chkili; M Yahyaoui
Journal:  J Med Genet       Date:  2006-01-06       Impact factor: 6.318

Review 3.  Sensory neuropathy in hereditary spastic paraplegia.

Authors:  W Schady; C M Smith
Journal:  J Neurol Neurosurg Psychiatry       Date:  1994-06       Impact factor: 10.154

4.  Peroneal muscular atrophy with hereditary spastic paraparesis (HMSN V) is pathologically heterogeneous. Report of nerve biopsy in four cases and review of the literature.

Authors:  F Gemignani; D Guidetti; P Bizzi; P Preda; G Cenacchi; A Marbini
Journal:  Acta Neuropathol       Date:  1992       Impact factor: 17.088

5.  Strumpell's pure familial spastic paraplegia: case study and review of the literature.

Authors:  G L Holmes; B A Shaywitz
Journal:  J Neurol Neurosurg Psychiatry       Date:  1977-10       Impact factor: 10.154
  5 in total

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