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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 […]

EAN 2017 – Peter Goadsby Interview

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Published Online: Jul 2nd 2017

Prof. Peter Goadsby talks to us about premonitory-like symptomatology in migraine, the focus of his article recently published in European Neurological Review.

View his article here.

 

Speaker disclosures: nothing to disclose in relation to this video interview.

 

Filmed at the 3rd Congress of the European Academy of Neurology (EAN), Amsterdam, June 2017.

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