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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 […]

‘two-step approach’ for MS treatments-significant effect on immunity

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Published Online: May 4th 2014

Speaker: Hideki Garren, Roche (EFPIA)

Session 4: The population in multiple sclerosis and the staggered ‘two-step approach’

Workshop on the clinical investigation of new medicines for the treatment of multiple sclerosis

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