Distinct clinical and pathological phenotypes in frontotemporal dementia associated with MAPT, PGRN and C9orf72 mutations-Reference-Cited by-同舟云学术

Distinct clinical and pathological phenotypes in frontotemporal dementia associated with MAPT, PGRN and C9orf72 mutations

Published:2015-10-16 Issue:7-8 Volume:16 Page:497-505
ISSN:2167-8421
Container-title:Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration
language:en
Short-container-title:Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration

Author:

Snowden Julie S.¹²,Adams Jennifer¹²,Harris Jennifer¹²,Thompson Jennifer C.¹²,Rollinson Sara²,Richardson Anna¹²,Jones Matthew¹²,Neary David¹,Mann David M.²,Pickering-Brown Stuart²

Affiliation:

1. Manchester Academic Health Sciences Centre, Cerebral Function Unit, Greater Manchester Neuroscience Centre, Salford Royal NHS Foundation Trust, Salford

2. Institute of Brain, Behaviour and Mental Health, Faculty of Human and Medical Sciences, University of Manchester, Manchester, UK

Publisher

Informa UK Limited

Subject

Neurology (clinical),Neurology

Link

https://www.tandfonline.com/doi/pdf/10.3109/21678421.2015.1074700

Reference40 articles.

1. Neuropathological background of phenotypical variability in frontotemporal dementia

2. Clinical, genetic and pathological heterogeneity of frontotemporal dementia: a review

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4. Sensitivity of revised diagnostic criteria for the behavioural variant of frontotemporal dementia

5. Syndromes of nonfluent primary progressive aphasia: A clinical and neurolinguistic analysis

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