An English kindred with a novel recessive tauopathy and respiratory failure-Reference-Cited by-同舟云学术

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An English kindred with a novel recessive tauopathy and respiratory failure

Published:2003-10-23 Issue:5 Volume:54 Page:682-686
ISSN:0364-5134
Container-title:Annals of Neurology
language:en
Short-container-title:Ann Neurol.

Author:

Nicholl David J.,Greenstone Michael A.,Clarke Carl E.,Rizzu Patrizia,Crooks Daniel,Crowe Alex,Trojanowski John Q.,Lee Virginia M.-Y.,Heutink Peter

Publisher

Wiley

Subject

Clinical Neurology,Neurology

Reference19 articles.

1. Neurodegenerative Tauopathies

2. Untangling tau-related dementia

3. Association of missense and 5′-splice-site mutations in tau with the inherited dementia FTDP-17

4. Tau is a candidate gene for chromosome 17 frontotemporal dementia

5. Mutation in the tau gene in familial multiple system tauopathy with presenile dementia

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1. C9orf72 genetic screening in amyotrophic lateral sclerosis patients from Serbia;Genetika;2023

2. FTD-associated mutations in Tau result in a combination of dominant and recessive phenotypes;Neurobiology of Disease;2022-08

3. Tau mRNA Metabolism in Neurodegenerative Diseases: A Tangle Journey;Biomedicines;2022-01-23

4. C9ORF72 repeat expansion is not associated with atypical parkinsonism in the Serbian population;Genetika;2022

5. Ondine's Curse in Frontotemporal Dementia with Parkinsonism Linked to Chromosome 17 Caused by MAPT Variants;Movement Disorders Clinical Practice;2021-06-24

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