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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 – Patrick Vermersch Interview – Part 3

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Published Online: May 11th 2017


Dr Patrick Vermersch gives us his thoughts on tailoring multiple sclerosis treatment to the individual patient. Part 3 of 3.

View part 1 here.

View part 2 here.

Speaker disclosures: Honoraria, consulting fees and research support from Roche, Biogen, Sanofi, Novartis, Servier, Merck, Alimera Sciences and Teva.

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

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