White matter lesions in FTLD: distinct phenotypes characterizeGRNandC9ORF72mutations-Reference-Cited by-同舟云学术

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White matter lesions in FTLD: distinct phenotypes characterizeGRNandC9ORF72mutations

Published:2016-01-28 Issue:1 Volume:2 Page:e47
ISSN:2376-7839
Container-title:Neurology Genetics
language:en
Short-container-title:Neurol Genet

Author:

Ameur Fatima,Colliot Olivier,Caroppo Paola,Ströer Sebastian,Dormont Didier,Brice Alexis,Azuar Carole,Dubois Bruno,Le Ber Isabelle,Bertrand Anne

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Genetics (clinical),Neurology (clinical)

Reference7 articles.

1. Extensive white matter involvement in patients with frontotemporal lobar degeneration: think progranulin;Caroppo;JAMA Neurol,2014

2. Prominent phenotypic variability associated with mutations in Progranulin

3. Mutations in progranulin (GRN) within the spectrum of clinical and pathological phenotypes of frontotemporal dementia

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

5. Clinical Significance of Lobar Atrophy in Frontotemporal Dementia: Application of an MRI Visual Rating Scale

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1. The role of brain perfusion SPECT in the diagnosis of frontotemporal dementia: A systematic review;Journal of Neuroimaging;2024-01-08

2. Atypical White Matter Hyperintensities Markedly Impact Plasma Neurofilament Light Chain Variability in GRN Patients;Journal of Alzheimer's Disease;2023-08-15

3. Disrupted myelin lipid metabolism differentiates frontotemporal dementia caused by GRN and C9orf72 gene mutations;Acta Neuropathologica Communications;2023-03-27

4. Dissecting the Many Faces of Frontotemporal Dementia: An Imaging Perspective;International Journal of Molecular Sciences;2022-10-25

5. Diagnóstico da demência frontotemporal: recomendações do Departamento Científico de Neurologia Cognitiva e do Envelhecimento da Academia Brasileira de Neurologia;Dementia & Neuropsychologia;2022-09

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