Recessively‐Inherited Adult‐Onset Alexander Disease Caused by a Homozygous Mutation in the GFAP Gene-Reference-Cited by-同舟云学术

Recessively‐Inherited Adult‐Onset Alexander Disease Caused by a Homozygous Mutation in the GFAP Gene

Published:2020-05-06 Issue:9 Volume:35 Page:1662-1667
ISSN:0885-3185
Container-title:Movement Disorders
language:en
Short-container-title:Mov Disord

Author:

Fu Mu‐Hui¹^ORCID,Chang Yung‐Yee¹²,Lin Ni‐Hsuan³,Yang Ai‐Wen³⁴,Chang Chiung‐Chih¹,Liu Jia‐Shou¹,Peng Cheng‐Huei¹,Wu Kay, L.H.⁵⁶,Perng Ming‐Der³⁴^ORCID,Lan Min‐Yu¹²

Affiliation:

1. Department of Neurology Chang Gung University College of Medicine Kaohsiung Taiwan

2. Center for Parkinson's Disease Kaohsiung Chang Gung Memorial Hospital, and Chang Gung University College of Medicine Kaohsiung Taiwan

3. Institute of Molecular Medicine, College of Life Sciences, National Tsing Hua University Hsinchu Taiwan

4. Department of Medical Science, College of Life Sciences National Tsing Hua University Hsinchu Taiwan

5. Institute for Translational Research in Biomedicine, Kaohsiung Chang Gung Memorial Hospital Kaohsiung Taiwan

6. Department of Senior Citizen Services National Tainan Institute of Nursing Tainan Taiwan

Funder

Ministry of Science and Technology, Taiwan

National Tsing Hua University

Publisher

Wiley

Subject

Neurology (clinical),Neurology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/mds.28099

Reference26 articles.

1. PROGRESSIVE FIBRINOID DEGENERATION OF FIBRILLARY ASTROCYTES ASSOCIATED WITH MENTAL RETARDATION IN A HYDROCEPHALIC INFANT

2. Alexander's disease: A report and reappraisal

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

4. Alexander disease: Ventricular garlands and abnormalities of the medulla and spinal cord

5. Adult-onset Alexander disease with typical "tadpole" brainstem atrophy and unusual bilateral basal ganglia involvement: a case report and review of the literature

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1. Adult-Onset Genetic Leukoencephalopathies With Movement Disorders;Journal of Movement Disorders;2023-05-31

2. Case report: Alexander's disease with “head drop” as the main symptom and literature review;Frontiers in Neurology;2022-12-19

3. Astrocyte contribution to dysfunction, risk and progression in neurodegenerative disorders;Nature Reviews Neuroscience;2022-10-31

4. Identification of a novel de novo pathogenic variant in GFAP in an Iranian family with Alexander disease by whole-exome sequencing;European Journal of Medical Research;2022-09-10

5. GFAP at 50;ASN Neuro;2020-01