Literature DB >> 553422

Myoencephalopathy: cerebral hypomyelination revealed by CT scan of the head in a muscle disease.

J P Bernier, M H Brooke, T P Naidich, J E Carroll.   

Abstract

Entities:  

Mesh：

Year:  1979        PMID： 553422

Source DB:  PubMed          Journal:  Trans Am Neurol Assoc        ISSN： 0065-9479


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  3 in total

1.  Changes in cerebral white matter in a case of congenital muscular dystrophy.

Authors:  J M Gobernado; A Gimeno
Journal:  Pediatr Radiol       Date:  1982

2.  Brain alterations in the classical form of congenital muscular dystrophy. Clinical and neuroimaging follow-up of 12 cases and correlation with the expression of merosin in muscle.

Authors:  C P Trevisan; F Martinello; E Ferruzza; M Fanin; M Chevallay; F M Tomé
Journal:  Childs Nerv Syst       Date:  1996-10       Impact factor: 1.475

3.  Congenital muscular dystrophy: brain alterations in an unselected series of Western patients.

Authors:  C P Trevisan; C Carollo; P Segalla; C Angelini; P Drigo; R Giordano
Journal:  J Neurol Neurosurg Psychiatry       Date:  1991-04       Impact factor: 10.154
  3 in total

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