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CLINICAL MANIFESTATIONS The clinical presentation buy levitra canada of FTLD is heterogeneous, driven by the variable involvement of the left or right frontal or temporal regions. Mann, South, Snowden, & Neary, 1991. Whereas SD is the least familial , fTD and FTD with amyotrophic lateral sclerosis are the most genetic forms of FTLD. Table 21.1 describes the demographic features of patients with the different FTLD subtypes.
Tolnay & Probst, 2003. Wilhelmsen, 1999). Additionally, the basal ganglia, motor neurons, and spinal cord are vulnerable in FTLD (Brun, 1985. 1997), tolnay & Probst.
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