Literature DB >> 14032261

Hereditary sensory neuropathy with spinal cord disease.

R R KHALIFEH, H ZELLWEGER.   

Abstract

Entities:  

Keywords:  PERIPHERAL NERVE DISEASES; SENSATION; SPINAL DISEASES; SPINAL NERVES

Mesh：

Year:  1963        PMID： 14032261     DOI： 10.1212/wnl.13.5.405

Source DB:  PubMed          Journal:  Neurology        ISSN： 0028-3878            Impact factor:   9.910


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  3 in total

1.  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 2.  Sensory neuropathy in hereditary spastic paraplegia.

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

3.  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
  3 in total

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