Cerebellar ataxia, anterior horn cell disease, learning difficulties, and dystonia: a new syndrome.
Author:
Publisher
Wiley
Subject
Neurology (clinical),Developmental Neuroscience,Pediatrics, Perinatology and Child Health
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1469-8749.2000.tb00042.x/fullpdf
Reference14 articles.
1. Pontocerebellar hypoplasias. An overview of a group of inherited neurodegenerative disorders with fetal onset;Barth;Brain and Development,1993
2. The syndrome of autosomal recessive pontocerebellar hypoplasia, microcephaly, and extrapyramidal dyskinesia (pontocerebellar hypoplasia type 2): compiled data from 10 pedigrees;Barth;Neurology,1995
3. Infantile olivopontocerebellar atrophy with spinal muscular atrophy (infantile OPCA +SMA);Chou;Clinical Neuropathology,1990
4. Olivopontocerebellar atrophy in children: a report of seven cases in two families;Colan;Annals of Neurology,1981
5. Olivopontocerebellar hypoplasia with anterior horn cell involvement (SMA) does not localise to chromosome 5q;Dubowitz;Neuromuscular Disorders,1995
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