Literature DB >> 4712933

Hallervorden-Spatz disease and infantile neuroaxonal dystrophy. Clinical characteristics and nosological considerations.

S Gilman, R E Barrett.   

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Year:  1973        PMID: 4712933     DOI: 10.1016/0022-510x(73)90162-7

Source DB:  PubMed          Journal:  J Neurol Sci        ISSN: 0022-510X            Impact factor:   3.181


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  6 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.  Atypical dopa responsive parkinsonism in a patient with megalencephaly, midbrain Lewy body disease, and some pathological features of Hallervorden-Spatz disease.

Authors:  P J Tuite; J P Provias; A E Lang
Journal:  J Neurol Neurosurg Psychiatry       Date:  1996-11       Impact factor: 10.154

3.  Infantile neuroaxonal dystrophy (Seitelberger's disease). A light and ultrastructural study.

Authors:  S Yagishita; S Kimura
Journal:  Acta Neuropathol       Date:  1975       Impact factor: 17.088

4.  Infantile neuroaxonal dystrophy or Seitelberger's disease. IV. Autonomic nervous system involvement: electron microscopic study in two siblings.

Authors:  M Berard-Badier; M Toga; D Gambarelli; J Hassoun; J F Pellissier; N Pinsard; R Bernard
Journal:  Acta Neuropathol       Date:  1974       Impact factor: 17.088

5.  Infantile neuroaxonal dystrophy. Histological and electron microscopical study of two cases.

Authors:  S Yagishita; S Kimura
Journal:  Acta Neuropathol       Date:  1974       Impact factor: 17.088

Review 6.  The genetics of primary torsion dystonia.

Authors:  U Müller; K G Kupke
Journal:  Hum Genet       Date:  1990-01       Impact factor: 4.132

  6 in total

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