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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 […]

AAN 2017 – Said Beydoun Interview – Part 2

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Published Online: May 12th 2017

 

Editor-in-Chief of US Neurology, Prof. Said Beydoun, reviews the differential diagnoses for multifocal motor neuropathy (MMN), and summarizes the emerging technologies for the diagnosis of MMN.
Part 2 of 2

View part 1 here.

Speaker disclosures: Consultant: Grifols, Shire. Speaker: Grifols. Research Grant: CSL

Filmed at the American Academy of Neurology (AAN) Annual Meeting, Boston, US, April 2017

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