By Michael J. Strong
Over the last ten years, there was an expanding popularity that syndromes of frontotemporal disorder (FTD) are a standard incidence in sufferers with amyotrophic lateral sclerosis (ALS). Such syndromes could be found in as many as 60% of sufferers with ALS. Conversely, the prevalence of motor neuron disorder in sufferers with clinically natural frontotemporal dementia is more and more famous. this means that to some degree there are overlapping syndromes during which either ALS and FTD happen in the comparable person.
This quantity summarizes the advances in our knowing of those issues, in addition to the aptitude dating among the 2. Key subject matters contain advances in our skill to clinically describe the frontotemporal syndromes, preclinical detection, neuroimaging, and genetics. The exploding box of latest markers in neuropathology is tested, as is the function of latest genetic mutations in DNA/RNA shipping platforms. This booklet is the fundamental reference textual content for this subject, and may be of curiosity to neurologists and neurological trainees with a medical or examine curiosity within the FTDs or ALS, neuropsychologists, neuropathologists, and researchers.
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Extra resources for Amyotrophic Lateral Sclerosis and the Frontotemporal Dementias
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