Adult‐onset Alexander disease with unusual inflammatory features and a novel GFAP mutation in two patients-Reference-Cited by-同舟云学术

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Adult‐onset Alexander disease with unusual inflammatory features and a novel GFAP mutation in two patients

Published:2023-08 Issue:4 Volume:49 Page:
ISSN:0305-1846
Container-title:Neuropathology and Applied Neurobiology
language:en
Short-container-title:Neuropathology Appl Neurobio

Author:

Ziad Fouzia¹^ORCID,Cypers Gert²,Phillips Matthew³,Vanhoenacker Piet⁴,Hostens Arne²,Yadavraj Satish³,Lamont Duncan¹,Robertson Thomas⁵

Affiliation:

1. Department of Pathology Waikato Hospital Hamilton New Zealand

2. Department of Neurology Onze‐Lieve‐Vrouwziekenhuis Aalst Belgium

3. Department of Neurology Waikato Hospital Hamilton New Zealand

4. Department of Radiology University Hospital Ghent Belgium

5. Pathology Queensland Royal Brisbane and Women's Hospital Herston Australia

Publisher

Wiley

Subject

Physiology (medical),Neurology (clinical),Neurology,Histology,Pathology and Forensic Medicine

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/nan.12927

Reference16 articles.

1. Alexander disease: models, mechanisms, and medicine

2. GFAP mutations, age at onset, and clinical subtypes in Alexander disease

3. Waisman Center.University of Wisconsin‐Madison. Alexander disease. GFAP mutations associated with Alexander disease. Available at:http://www.waisman.wisc.edu/alexander-disease

Cited by 1 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Alexander disease genetics: Beyond GFAP exon sequencing?;Journal of Neuropathology & Experimental Neurology;2023-11-21

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