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Joseph Samaha, Jim Dagher, Shayan Abdollah Zadegan

Huntington’s disease (HD) is a neurodegenerative disease inherited in an autosomal dominant manner. It is caused by an expansion of cytosine, adenine, guanine (CAG) repeats within the huntingtin (HTT) gene, which is located on chromosome 4. This pathological expansion of CAG repeats results in the production of a mutant huntingtin protein with an abnormally long polyglutamine […]

Assessing Cognitive Changes

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Published Online: Mar 1st 2016

Dr Frederick W. Foley and Dr Anthony Feinstein discuss the assessment of cognetive changes in multiple sclerosis.

Video credit: National MS Society.

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