Literature DB >> 14152212

FAMILIAL AMYOTROPHIC DYSTONIC PARAPLEGIA.

S GILMAN, S HORENSTEIN.   

Abstract

Entities:  

Keywords:  ADOLESCENCE; CHILD; ELECTROMYOGRAPHY; GENETICS, HUMAN; INFANT; MENTAL RETARDATION; MUSCULAR DISEASES; PARAPLEGIA

Mesh：

Year:  1964        PMID： 14152212     DOI： 10.1093/brain/87.1.51

Source DB:  PubMed          Journal:  Brain        ISSN： 0006-8950            Impact factor:   13.501


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  3 in total

1.  Mapping of a complicated familial spastic paraplegia to locus SPG4 on chromosome 2p.

Authors:  O Heinzlef; C Paternotte; F Mahieux; J F Prud'homme; J Dien; M Madigand; J Pouget; J Weissenbach; E Roullet; J Hazan
Journal:  J Med Genet       Date:  1998-02       Impact factor: 6.318

2.  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

3.  CT scan in a case of progressive generalized dystonia with amyotrophic paraplegia.

Authors:  R D'Alessandro; P Tinuper; A Lozito; T Sacquegna; P Cortelli; P Pazzaglia
Journal:  Ital J Neurol Sci       Date:  1983-09
  3 in total

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