Agraphia in patients with frontotemporal dementia and parkinsonism linked to chromosome 17 with P301L MAPT mutation: dysexecutive, aphasic, apraxic or spatial phenomenon?

Παρόμοια τεκμήρια

• A Novel MAPT Mutation, G55R, in a Frontotemporal Dementia Patient Leads to Altered Tau Function
  ανά: Iyer, Abhinaya, κ.ά.
  Έκδοση: (2013)
• Drawing analysis in the assessment of patients with neurodegenerative diseases
  ανά: Sitek, Emilia J., κ.ά.
  Έκδοση: (2017)
• Apraxic agraphia: An insight into the writing disturbances of posterior aphasias
  ανά: Krishnan, Gopee, κ.ά.
  Έκδοση: (2009)
• Neuroimaging in the Differential Diagnosis of Primary Progressive Aphasia – Illustrative Case Series in the Light of New Diagnostic Criteria
  ανά: Sitek, Emilia J., κ.ά.
  Έκδοση: (2014)
• A Patient with Posterior Cortical Atrophy Possesses a Novel Mutation in the Presenilin 1 Gene
  ανά: Sitek, Emilia J., κ.ά.
  Έκδοση: (2013)