Gelsolin variant amyloidosis mimicking progressive bulbar palsy-Reference-Cited by-同舟云学术

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Gelsolin variant amyloidosis mimicking progressive bulbar palsy

Published:2022-09-21 Issue:5 Volume:66 Page:
ISSN:0148-639X
Container-title:Muscle & Nerve
language:en
Short-container-title:Muscle and Nerve

Author:

Park Jinseok¹²^ORCID,Kim Young‐Eun³,Oh Ki‐Wook¹²,Nahm Minyeop⁴,Kim Yu Jeong⁵,Kim Mi Jung⁶,Kim Seung Hyun¹²

Affiliation:

1. Department of Neurology College of Medicine, Hanyang University Seoul South Korea

2. Cell Therapy Center Hanyang University Hospital Seoul South Korea

3. Department of Laboratory Medicine College of Medicine, Hanyang University Seoul South Korea

4. Dementia Research Group, Korea Brain Research Institute Daegu South Korea

5. Department of Ophthalmology Hanyang University College of Medicine Seoul South Korea

6. Department of Rehabilitation Medicine Hanyang University College of Medicine Seoul South Korea

Funder

National Research Foundation of Korea

Publisher

Wiley

Subject

Physiology (medical),Cellular and Molecular Neuroscience,Neurology (clinical),Physiology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/mus.27714

Reference6 articles.

1. Natural course of Finnish gelsolin amyloidosis

2. Hereditary gelsolin amyloidosis (HGA): a neglected cause of bilateral progressive or recurrent facial palsy

3. Clinical and Histopathological Features of Gelsolin Amyloidosis Associated with a Novel GSN Variant p.Glu580Lys

4. Exome sequencing establishes a gelsolin mutation as the cause of inherited bulbar‐onset neuropathy

5. El Escorial revisited: Revised criteria for the diagnosis of amyotrophic lateral sclerosis

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