Literature DB >> 4662801

[Infantile neuro-axonal dystrophy and Hallervorden-Spatz disease. Electro-clinical and anatomo-pathological and differential diagnostic aspects].

J Radermecker, J J Martin.   

Abstract

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Year:  1972        PMID： 4662801

Source DB:  PubMed          Journal:  Bull Acad R Med Belg        ISSN： 0001-4168


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  3 in total

Review 1.  Clinical and genetic delineation of neurodegeneration with brain iron accumulation.

Authors:  A Gregory; B J Polster; S J Hayflick
Journal:  J Med Genet       Date:  2008-11-03       Impact factor: 6.318

2.  Skin and conjunctival biopsies in infantile neuroaxonal dystrophy.

Authors:  J J Martin; J G Leroy; J Libert; M van Eygen; N Logghe
Journal:  Acta Neuropathol       Date:  1979-03-15       Impact factor: 17.088

3.  Generalized giant axonal neuropathy: a filament-forming disease of neuronal, endothelial, glial, and schwann cells in a patient without kinky hair.

Authors:  J Peiffer; W Schlote; A Bischoff; E Boltshauser; G Müller
Journal:  Acta Neuropathol       Date:  1977-11-28       Impact factor: 17.088
  3 in total

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