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Publications by Emilia J. Sitek

A Patient With Posterior Cortical Atrophy Possesses a Novel Mutation in the Presenilin 1 Gene

Multidisciplinary

English

Agraphia in Patients With Frontotemporal Dementia and Parkinsonism Linked to Chromosome 17 With P301LMAPTmutation: Dysexecutive, Aphasic, Apraxic or Spatial Phenomenon?

English