By Michael J. Strong
in which either ALS and FTD happen in the comparable individual.
This quantity summarizes the advances in our knowing of those problems, in addition to the capability dating among the 2. Key themes comprise advances in our skill to clinically describe the frontotemporal syndromes, preclinical detection, neuroimaging, and genetics. The exploding box of recent markers in neuropathology is tested, as is the function of latest genetic mutations in DNA/RNA shipping platforms. This ebook is the basic reference textual content for this subject, and should be of
interest to neurologists and neurological trainees with a scientific or study curiosity within the FTDs or ALS, neuropsychologists, neuropathologists, and researchers.
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During the last ten years, there was an expanding acceptance that syndromes of frontotemporal disorder (FTD) are a standard prevalence in sufferers with amyotrophic lateral sclerosis (ALS). Such syndromes should 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.
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Amyotrophic Lateral Sclerosis and the Frontotemporal Dementias by Michael J. Strong
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