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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 […]

Henry Ma, ESOC 2019 – Meta-analysis of EXTEND, ECASS4-EXTEND and EPITHET trials

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Published Online: Jun 12th 2019

Henry Ma, on behalf of the EXTEND (Extending the Time for Thrombolysis in Emergency Neurological Deficits [International], NCT01580839), ECASS4-EXTEND (European Cooperative Acute Stroke Study-4: Extending the time for thrombolysis in emergency neurological deficits, ISRCTN71616222) and EPITHET (Echoplanar Imaging Thrombolysis Evaluation Trial, NCT00238537) Investigators, discusses important results presented at ESOC 2019 from a meta-analysis of individual patient data from these trials.

Content produced in Milan, Italy and shared with kind authorisation of the European Stroke Organisation (ESO) and the European Stroke Organisation Conference (ESOC 2019). 

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