Maria Stamelou MD, PhD, Movement Disorders, Volume 31, Issue 1, pages 7–8, January 2016, DOI: 10.1002/mds.26508
One should not forget that FA may present later in life with a predominant nonataxic phenotype, such as with a Huntington’s disease phenocopy. Moreover, future studies should provide larger number of patients and more detailed clinical information on further neurological signs such as cognition or autonomic function.
Sunday, January 24, 2016
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