Co‐incidental C9orf72 expansion mutation‐related frontotemporal lobar degeneration pathology and sporadic Creutzfeldt−Jakob disease-Reference-Cited by-同舟云学术

Co‐incidental C9orf72 expansion mutation‐related frontotemporal lobar degeneration pathology and sporadic Creutzfeldt−Jakob disease

Published:2020-12 Issue:3 Volume:28 Page:1009-1015
ISSN:1351-5101
Container-title:European Journal of Neurology
language:en
Short-container-title:Eur J Neurol

Author:

Klotz Sigrid¹²^ORCID,König Theresa³,Erdler Marcus⁴,Ulram Andreas⁵,Nguyen Anita¹,Ströbel Thomas¹²,Zimprich Alexander³,Stögmann Elisabeth³,Regelsberger Günther¹²,Höftberger Romana¹,Budka Herbert¹²,Kovacs Gabor G.⁶⁷⁸^ORCID,Gelpi Ellen¹²^ORCID

Affiliation:

1. Division of Neuropathology and Neurochemistry Department of Neurology Medical University of Vienna Vienna Austria

2. Austrian Reference Center for Human Prion Diseases (OERPE) Vienna Austria

3. Department of Neurology Medical University of Vienna Vienna Austria

4. Department of Neurology Klinik Donaustadt mit Ludwig‐Boltzmann‐Institut Vienna Austria

5. Department of Neurosurgery Krankenanstalt Rudolfstiftung Vienna Austria

6. Tanz Centre for Research in Neurodegenerative Disease University of Toronto Toronto ON Canada

7. Department of Laboratory Medicine and Pathobiology and Department of Medicine University of Toronto Toronto ON Canada

8. Laboratory Medicine Program & Krembil Brain Institute University Health Network Toronto ON Canada

Publisher

Wiley

Subject

Neurology (clinical),Neurology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/ene.14621

Reference48 articles.

1. Clinical and pathological features of familial frontotemporal dementia caused by C9ORF72 mutation on chromosome 9p

2. The neuropathology associated with repeat expansions in the C9ORF72 gene

3. Large C9orf72 Hexanucleotide Repeat Expansions Are Seen in Multiple Neurodegenerative Syndromes and Are More Frequent Than Expected in the UK Population

4. Corticobasal and ataxia syndromes widen the spectrum ofC9ORF72hexanucleotide expansion disease

5. Distinct clinical and pathological characteristics of frontotemporal dementia associated with C9ORF72 mutations

Cited by 2 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. Metabolic Brain Changes Can Predict the Underlying Pathology in Neurodegenerative Brain Disorders: A Case Report of Sporadic Creutzfeldt–Jakob Disease with Concomitant Parkinson’s Disease;International Journal of Molecular Sciences;2023-08-23

2. Cerebrospinal Fluid Biomarker Profile in TDP-43-Related Genetic Frontotemporal Dementia;Journal of Personalized Medicine;2022-10-21