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- W1998312103 abstract "<b>Objective:</b> Spinocerebellar ataxia type 6 (SCA6) is a rare autosomal dominant neurodegenerative movement disorder, part of the group of CAG repeat diseases. Parkinsonism has been reported in SCA6 as well as several other SCAs, but pathological information regarding this association has been rarely described in the literature. - <b>Background:</b> The patient was a 69-year-old woman, who presented with gait ataxia and diagnosed with SCA6 expansion of 22 repeats. She then developed a unilateral resting hand tremor that was partially levodopa-responsive. She subsequently deteriorated rapidly, becoming immobile with rapid cognitive decline and died three years later. - <b>Methods:</b> Laboratory ataxia evaluation and restricted autopsy performed at the request of the patient9s family to evaluate for concomitant neurodegenerative disorders. - <b>Results:</b> Histological examination of the brain confirmed substantial Purkinje cell loss, typically found in cases of SCA6. Polyglutamine related inclusions were not seen, but rather, typical Lewy body pathology and loss of pigmented neurons was found in substantia nigra and other brain stem regions. - <b>Conclusions:</b> These results suggest that parkinsonism associated with SCA6 is pathologically similar to idiopathic Parkinson9s disease. <b>Disclosure:</b> Dr. Kaul has nothing to disclose. Dr. Morley has nothing to disclose. Dr. Pakalniskis has nothing to disclose. Dr. Hickey has nothing to disclose. Dr. Lee has nothing to disclose." @default.
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- W1998312103 title "Sulphur bath and mud pack treatment for rheumatoid arthritis at the Dead Sea area." @default.
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- W1998312103 doi "https://doi.org/10.1136/ard.49.2.99" @default.
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