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Serum Neurofilament Light in Patients with Frontotemporal Dementia Caused by CHMP2B Mutation

Serum Neurofilament Light in Patients with Frontotemporal Dementia Caused by CHMP2B Mutation

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_crossref_primary_10_1159_000513877

Serum Neurofilament Light in Patients with Frontotemporal Dementia Caused by CHMP2B Mutation

About this item

Full title

Serum Neurofilament Light in Patients with Frontotemporal Dementia Caused by CHMP2B Mutation

Publisher

Basel, Switzerland: S. Karger AG

Journal title

Dementia and geriatric cognitive disorders, 2021-04, Vol.49 (6), p.533-538

Language

English

Formats

Publication information

Publisher

Basel, Switzerland: S. Karger AG

More information

Scope and Contents

Contents

Introduction: The potential of neurofilament light (NfL) as a blood-based biomarker is currently being investigated in autosomal dominant neurodegenerative disease. This study explores the clinical utility of serum-NfL in frontotemporal dementia due to CHMP2B mutation (FTD-3). Methods: This cross-sectional study included serum and CSF data from 38...

Alternative Titles

Full title

Serum Neurofilament Light in Patients with Frontotemporal Dementia Caused by CHMP2B Mutation

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_crossref_primary_10_1159_000513877

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_crossref_primary_10_1159_000513877

Other Identifiers

ISSN

1420-8008

E-ISSN

1421-9824

DOI

10.1159/000513877

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