FTLD-TDP with motor neuron disease, visuospatial impairment and a progressive supranuclear palsy-like syndrome: broadening the clinical phenotype of TDP-43 proteinopathies. A report of three cases
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J. Hort | I. Holmerová | G. Kovacs | R. Rusina | P. Ridzoň | R. Matěj | T. Ströbel | Jindřich Fiala