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See Latest ArticlesPurkinje Cell Loss in the Cerebellar Flocculus in Patients with Ataxia with Ocular Motor Apraxia Type 1/Early-Onset Ataxia with Ocular Motor Apraxia and Hypoalbuminemia
European Neurology, 10/11/07
Sugawara, M., et al. - We genetically screened patients with ataxia with ocular motor apraxia type 1 (AOA1)/early-onset ataxia with ocular motor apraxia and hypoalbuminemia (EAOH), with a Japanese variant form of Friedreich's ataxia. Three patients were found to have a homozygous insertion mutation of the aprataxin gene (689insT). An elder sister of a patient in this series died of cerebral hemorrhage at the age of 45, and underwent autopsy
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Posterior Reversible Encephalopathy Syndrome - Long-term follow-up
Journal of Neurology, Neurosurgery, and Psychiatry , 12/18/09
Improving fatigue assessment in immune-mediated neuropathies: the modified Rasch-built fatigue severity scale
Journal of the Peripheral Nervous System, 12/18/09
The profile of motor unit number estimation (MUNE) in spinal and bulbar muscular atrophy
Journal of Neurology, Neurosurgery, and Psychiatry , 12/18/09
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