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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 […]

Revised Consensus Statement on Restless Legs Syndrome

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Published Online: Apr 6th 2014

Dr. Michael Silber, a Professor of Neurology at Mayo Clinic in Rochester, MN, and Chair of the Willis-Ekbom Disease Foundation Medical Advisory Board, in the September 2013 issue of Mayo Clinic Proceedings, provides an updated consensus recommendation on the management of restless legs syndrome (Willis-Ekbom disease), noting new treatment options and greater understanding for patients with this common, underdiagnosed, and often misunderstood condition.

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