A new MAPT deletion in a case of speech apraxia leading to corticobasal syndrome-Reference-Cited by-同舟云学术

A new MAPT deletion in a case of speech apraxia leading to corticobasal syndrome

Published:2018-05-04 Issue:3 Volume:24 Page:140-144
ISSN:1355-4794
Container-title:Neurocase
language:en
Short-container-title:Neurocase

Author:

Mazzon Giulia¹^ORCID,Menichelli Alina²,Fabretto Antonella³,Cattaruzza Tatiana¹,Manganotti Paolo¹

Affiliation:

1. Neurological Clinic, Department of Medical, Surgical and Health Sciences, University of Trieste, Trieste, Italy

2. Neuropsychology Unit, Department of Rehabilitation Medicine, University of Trieste, Trieste, Italy

3. Department of Advanced Diagnostic and Clinical Trials – Medical Genetics, Institute for Maternal and Child Health – IRCCS Burlo Garofolo, Trieste, Italy

Publisher

Informa UK Limited

Subject

Neurology (clinical),Arts and Humanities (miscellaneous)

Link

https://www.tandfonline.com/doi/pdf/10.1080/13554794.2018.1492729

Reference37 articles.

1. Validation of the new consensus criteria for the diagnosis of corticobasal degeneration

2. The Frontal Assessment Battery (FAB): normative values in an Italian population sample

3. Criteria for the diagnosis of corticobasal degeneration

4. Progressive Crossed-Apraxia of Speech as a First Manifestation of a Probable Corticobasal Degeneration

5. “Whose face is this?”: Italian norms of naming celebrities

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