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Quoted phrase not found in phrase index: "Neurodegeneration with ataxia and late-onset optic atrophy"
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The clinical features and classification of the late onset autosomal dominant cerebellar ataxias. A study of 11 families, including descendants of the 'the Drew family of Walworth'.
Harding AE. Harding AE. Brain. 1982 Mar;105(Pt 1):1-28. doi: 10.1093/brain/105.1.1. Brain. 1982. PMID: 7066668
The clinical features of 11 families containing 73 individuals with dominantly inherited cerebellar ataxia of late onset are described. Many of the patients had physical signs in addition to cerebellar ataxia, which included dementia, supranuclear opht …
The clinical features of 11 families containing 73 individuals with dominantly inherited cerebellar ataxia of late onset …
Clinical spectrum of Hallervorden-Spatz syndrome in India.
Sachin S, Goyal V, Singh S, Shukla G, Sharma MC, Gaikwed S, Behari M. Sachin S, et al. J Clin Neurosci. 2009 Feb;16(2):253-8. doi: 10.1016/j.jocn.2008.04.004. Epub 2008 Dec 3. J Clin Neurosci. 2009. PMID: 19056277
The patients with early onset had more frequent truncal and axial dystonia, including retrocollis, oromandibular-facial dystonia and chorea, dysarthria, pyramidal signs, gait disturbance, cognitive impairment, delay in milestones, retinitis pigmentosa, optic atrophy …
The patients with early onset had more frequent truncal and axial dystonia, including retrocollis, oromandibular-facial dystonia and chorea, …