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Therapeutic Approaches for the Treatment of Chorea in Huntington’s Disease

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 […]

touchREVIEWS in Neurology. 2025;21(1):Online ahead of journal publication

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THE EVOLVING MANAGEMENT OF ADVANCED PARKINSON’S DISEASE – SUMMER 2012

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MULTIPLE SCLEROSIS – INSIGHTS FOR 2013 – SUMMER 2013

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