Literature DB >> 5173359

Hereditary disease of the cerebellar parenchyma.

L P Weiner, B W Konigsmark.   

Abstract

Hereditary diseases involving primarily the cerebellar parenchyma, namely the molecular and granular layers, Purkinje cells and subcortical cerebellar nuclei, are classified.

Entities:  

Mesh：

Year:  1971        PMID： 5173359

Source DB:  PubMed          Journal:  Birth Defects Orig Artic Ser        ISSN： 0547-6844


  3 in total

1.  Infantile cerebello-optic atrophy. Neuropathology of the progressive encephalopathy syndrome with edema, hypsarrhythmia and optic atrophy (the PEHO syndrome).

Authors:  M Haltia; M Somer
Journal:  Acta Neuropathol       Date:  1993       Impact factor: 17.088

2.  Genetic aspects of autosomal dominant late onset cerebellar ataxia.

Authors:  A E Harding
Journal:  J Med Genet       Date:  1981-12       Impact factor: 6.318

3.  Hereditary cerebellar atrophy (Holmes type) with optic atrophy: a clinico-pathological study of four generations in a family.

Authors:  H Budka; D Seemann; W Danielczyk
Journal:  Arch Psychiatr Nervenkr (1970)       Date:  1979-04-12
  3 in total

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