Literature DB >> 5691597

Infantile neuroaxonal dystrophy and its relationship to Hallervorden-Spatz disease.

S Indravasu, R A Dexter.   

Abstract

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Year:  1968        PMID： 5691597     DOI： 10.1212/wnl.18.7.693

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


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  3 in total

1.  Infantile neuroaxonal dystrophy. An electron microscopic study of a case clinically resembling neuronal ceroid-lipofuscinosis.

Authors:  J F Butzer; S S Schochet; W E Bell
Journal:  Acta Neuropathol       Date:  1975       Impact factor: 17.088

2.  [A contribution concerning the infantile neuro-axonal dystrophy. Comparison to Hallervorden-Spatz disease regarding histopathologic findings and clinical symptoms].

Authors:  E Richter
Journal:  Z Neurol       Date:  1972

3.  Neuroaxonal dystrophy. A case of non pigmented type and protracted course.

Authors:  J Thibault
Journal:  Acta Neuropathol       Date:  1972       Impact factor: 17.088
  3 in total

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