By Michael J. Strong
During the last ten years, there was an expanding popularity that syndromes of frontotemporal disorder (FTD) are a typical prevalence in sufferers with amyotrophic lateral sclerosis (ALS). Such syndromes might 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 well-known. this implies that to some degree there are overlapping syndromes within which either ALS and FTD ensue in the related person.
This quantity summarizes the advances in our knowing of those problems, in addition to the aptitude dating among the 2. Key subject matters 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 delivery structures. This publication is the fundamental reference textual content for this subject, and may be of curiosity to neurologists and neurological trainees with a scientific or study curiosity within the FTDs or ALS, neuropsychologists, neuropathologists, and researchers.
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Additional resources for Amyotrophic Lateral Sclerosis and the Frontotemporal Dementias
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