Literature DB >> 13180188

Concordant primary atrophy of the cerebellar granules in monozygotic twins.

G A JERVIS.   

Abstract

Entities:  

Keywords:  BRAIN/diseases; TWINS/diseases

Mesh：

Year:  1954        PMID： 13180188     DOI： 10.1017/s1120962300021284

Source DB:  PubMed          Journal:  Acta Genet Med Gemellol (Roma)        ISSN： 0001-5660


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  4 in total

1.  [A case of primary systemic atrophy of the cerebellar cortex of the granular type in familial congenital cerebellar syndrome (Norman, Jervis, Ule)].

Authors:  E GROB
Journal:  Dtsch Z Nervenheilkd       Date:  1961

2.  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

3.  Early degeneration of the cerebellar cortex, particularly the granular cells.

Authors:  O Bugiani; A Berio; A Di Stefano; G Mangiante; G L Mancardi; A Leonardi
Journal:  J Neurol       Date:  1978-12-07       Impact factor: 4.849

4.  MRI in cerebellar hypoplasia.

Authors:  N deSouza; R Chaudhuri; J Bingham; T Cox
Journal:  Neuroradiology       Date:  1994       Impact factor: 2.804
  4 in total

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