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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 […]

Neurosurgery and Epilepsy

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Published Online: Jul 22nd 2014

Professor John Duncan, Medical Director of the UK Epilepsy Society, discusses how epilepsy symptoms can be minimized with greater awareness of the condition among patients and physicians.

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