<scp><i>MAPT</i></scp>‐Associated Familial Progressive Supranuclear Palsy with Typical Corticobasal Degeneration Neuropathology: A Clinicopathological Report-Reference-Cited by-同舟云学术

MAPT‐Associated Familial Progressive Supranuclear Palsy with Typical Corticobasal Degeneration Neuropathology: A Clinicopathological Report

Published:2023-03-11 Issue:4 Volume:10 Page:691-694
ISSN:2330-1619
Container-title:Movement Disorders Clinical Practice
language:en
Short-container-title:Movement Disord Clin Pract

Author:

Cullinane Patrick W.¹²^ORCID,Fumi Riona¹,Theilmann Jensen Marte¹,Jabbari Edwin¹^ORCID,Warner Thomas T.¹²³^ORCID,Revesz Tamas²,Morris Huw R.¹³^ORCID,Rohrer Jonathan D.⁴,Jaunmuktane Zane¹²⁵

Affiliation:

1. Department of Clinical and Movement Neurosciences UCL Queen Square Institute of Neurology, University College London London UK

2. Queen Square Brain Bank for Neurological Disorders, UCL Queen Square Institute of Neurology London UK

3. Queen Square Movement Disorders Centre UCL Queen Square Institute of Neurology London UK

4. Dementia Research Centre UCL Queen Square Institute of Neurology, University College London London UK

5. Division of Neuropathology, National Hospital for Neurology and Neurosurgery University College London NHS Foundation Trust London UK

Publisher

Wiley

Subject

Neurology (clinical),Neurology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/mdc3.13706

Reference10 articles.

1. Criteria for the diagnosis of corticobasal degeneration

2. Novel mutation in MAPT exon 13 (p.N410H) causes corticobasal degeneration

3. Novel L284R MAPT Mutation in a Family with an Autosomal Dominant Progressive Supranuclear Palsy Syndrome

4. Clinical diagnosis of progressive supranuclear palsy: The movement disorder society criteria

5. Retiring the term FTDP-17 as MAPT mutations are genetic forms of sporadic frontotemporal tauopathies

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