Neuroimaging Pearls from the <scp>MDS</scp> Congress Video Challenge. Part 1: Genetic Disorders-Reference-Cited by-同舟云学术

Neuroimaging Pearls from the MDS Congress Video Challenge. Part 1: Genetic Disorders

Published:2022-02-03 Issue:3 Volume:9 Page:297-310
ISSN:2330-1619
Container-title:Movement Disorders Clinical Practice
language:en
Short-container-title:Movement Disord Clin Pract

Author:

Olszewska Diana A.¹^ORCID,Rawal Sapna²,Fearon Conor¹,Alcaide‐Leon Paula²,Stell Rick³,Paramanandan Vijayashankar⁴,Lynch Tim⁵⁶,Jawad Tania⁷,Vittal Padmaja⁸,Barton Brandon⁹¹⁰,Miyajima Hiroaki¹¹,Kono Satoshi¹²,Kandadai Rukmini Mridula¹³^ORCID,Borgohain Rupam¹³,Lang Anthony E.¹

Affiliation:

1. Edmond J. Safra Program in Parkinson's Disease, Morton and Gloria Shulman Movement Disorders Clinic, Toronto Western Hospital—UHN, Division of Neurology University of Toronto Toronto Ontario Canada

2. Division of Neuroradiology, Joint Department of Medical Imaging, Toronto Western Hospital University Health Network Toronto Ontario Canada

3. Movement Disorders Unit, Perron Institute of Neurological Translational Science Sir Charles Gairdner Hospital Perth Western Australia Australia

4. Apollo Hospitals Chennai India

5. Centre for Brain Health Dublin Neurological Institute at the Mater Misericordiae University Hospital Dublin Ireland

6. School of Medicine and Medical Science University College Dublin Dublin Ireland

7. Department of Neurology The Royal Free Hospital London United Kingdom

8. Northwestern Medicine Central Dupage Hospital Neurodegenerative Diseases Center Winfield Illinois USA

9. Rush University Medical Center Chicago Illinois USA

10. Parkinson's Disease Research, Education, and Clinical Care Consortium Jesse Brown VA Medical Center Chicago Illinois USA

11. First Department of Medicine Hamamatsu University School of Medicine Hamamatsu Japan

12. Kono Neurology Clinic Hamamatsu Japan

13. Department of Neurology Nizam's Institute of Medical Sciences Hyderabad India

Publisher

Wiley

Subject

Neurology (clinical),Neurology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/mdc3.13412

Reference79 articles.

1. We‐102. Adult onset Alexander's disease with cognitive impairment and autosomal dominant transmission associated with a novel mutation in the GFAP gene. Abstracts of the Movement Disorder Society's thirteenth international congress of Parkinson's disease and movement disorders;Rodrigues JP;Movement Dis,2009

2. Molecular findings in symptomatic and pre-symptomatic Alexander disease patients

3. Adult-onset Alexander disease: a series of eleven unrelated cases with review of the literature

4. Can MR Imaging Diagnose Adult-Onset Alexander Disease?

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