Literature DB >> 13762790

Familial diffuse progressive encephalopathy.

M C LIU, P E SYLVESTER.   

Abstract

Entities:  

Keywords:  BRAIN/diseases

Mesh：

Year:  1960        PMID： 13762790      PMCID： PMC2012552          DOI： 10.1136/adc.35.182.345

Source DB:  PubMed          Journal:  Arch Dis Child        ISSN： 0003-9888            Impact factor:   3.791


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  3 in total

1.  The cerebral atrophies and encephalomalacias of infancy and childhood.

Authors:  A WOLF; D COWEN
Journal:  Res Publ Assoc Res Nerv Ment Dis       Date:  1955

2.  Unusual form of cerebellar ataxia with sex-linked inheritance.

Authors:  N MALAMUD; P COHEN
Journal:  Neurology       Date:  1958-04       Impact factor: 9.910

3.  Familial degeneration of the cerebral gray matter in childhood with convulsions, myoclonus, spasticity, cerebellar ataxia, choreoathetosis, dementia, and death in status epilepticus; differentiation of infantile and juvenile types.

Authors:  F R FORD; S LIVINGSTON; C PRYLES
Journal:  J Pediatr       Date:  1951-07       Impact factor: 4.406
  3 in total
  2 in total

1.  Spongy glio-neuronal dystrophy in infancy and childhood.

Authors:  K Jellinger; F Seitelberger
Journal:  Acta Neuropathol       Date:  1970       Impact factor: 17.088

2.  Progressive neuronal degeneration of childhood (Alpers syndrome) with hepatic cirrhosis.

Authors:  D C Wilson; D McGibben; E M Hicks; I V Allen
Journal:  Eur J Pediatr       Date:  1993-03       Impact factor: 3.183
  2 in total

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