Literature DB >> 4795738

Sphincter involvement in hereditary spastic paraplegia.

N E Cartlidge, G Bone.   

Abstract

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Year:  1973        PMID： 4795738     DOI： 10.1212/wnl.23.11.1160

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


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  6 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

Review 2.  Pure hereditary spastic paraplegia.

Authors:  E Reid
Journal:  J Med Genet       Date:  1997-06       Impact factor: 6.318

3.  Novel locus for autosomal dominant hereditary spastic paraplegia, on chromosome 8q.

Authors:  P Hedera; S Rainier; D Alvarado; X Zhao; J Williamson; B Otterud; M Leppert; J K Fink
Journal:  Am J Hum Genet       Date:  1999-02       Impact factor: 11.025

4.  Autosomal dominant familial spastic paraplegia: tight linkage to chromosome 15q.

Authors:  J K Fink; C T Wu; S M Jones; G B Sharp; B M Lange; A Lesicki; T Reinglass; T Varvil; B Otterud; M Leppert
Journal:  Am J Hum Genet       Date:  1995-01       Impact factor: 11.025

5.  Hereditary "pure" spastic paraplegia: a clinical and genetic study of 22 families.

Authors:  A E Harding
Journal:  J Neurol Neurosurg Psychiatry       Date:  1981-10       Impact factor: 10.154

6.  Urodynamic evaluation of patients with autosomal dominant pure spastic paraplegia linked to chromosome 2p21-p24.

Authors:  L N Jensen; T Gerstenberg; E B Kallestrup; P Koefoed; J Nordling; J E Nielsen
Journal:  J Neurol Neurosurg Psychiatry       Date:  1998-11       Impact factor: 10.154
  6 in total

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