Literature DB >> 2725881

Agenesis of the corpus callosum: a marker for inherited metabolic disease?

E H Kolodny1.   

Abstract

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Year:  1989        PMID： 2725881     DOI： 10.1212/wnl.39.6.847

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


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  4 in total

1.  Callosal dysgenesis in a patient with Coffin-Lowry syndrome.

Authors:  A Ozden; E Dirik; A Emel; N Sevinc
Journal:  Indian J Pediatr       Date:  1994 Jan-Feb       Impact factor: 1.967

2.  Hypoplasia of the corpus callosum in Niemann-Pick type C disease.

Authors:  S Palmeri; C Battisti; A Federico; G C Guazzi
Journal:  Neuroradiology       Date:  1994       Impact factor: 2.804

3.  Pyruvate dehydrogenase (PDH) deficiency caused by a 21-base pair insertion mutation in the E1 alpha subunit.

Authors:  L De Meirleir; W Lissens; E Vamos; I Liebaers
Journal:  Hum Genet       Date:  1992-03       Impact factor: 4.132

4.  Severe psychiatric disturbance and abnormalities of the corpus callosum: review and case series.

Authors:  A S David; A Wacharasindhu; W A Lishman
Journal:  J Neurol Neurosurg Psychiatry       Date:  1993-01       Impact factor: 10.154
  4 in total

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