Diagnostic value of cerebrospinal fluid neurofilament light protein in neurology: a systematic review and meta-analysis

C Bridel, WN Van Wieringen, H Zetterberg… - JAMA …, 2019 - jamanetwork.com
Importance Neurofilament light protein (NfL) is elevated in cerebrospinal fluid (CSF) of a
number of neurological conditions compared with healthy controls (HC) and is a candidate …

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

H Seelaar, JD Rohrer, YAL Pijnenburg… - Journal of Neurology …, 2011 - jnnp.bmj.com
Frontotemporal dementia (FTD) is the second most common young-onset dementia and is
clinically characterised by progressive behavioural change, executive dysfunction and …

Tauopathies with parkinsonism: clinical spectrum, neuropathologic basis, biological markers, and treatment options

AC Ludolph, J Kassubek… - European journal of …, 2009 - Wiley Online Library
Tauopathies with parkinsonism represent a spectrum of disease entities unified by the
pathologic accumulation of hyperphosphorylated tau protein fragments within the central …

[PDF][PDF] A hexanucleotide repeat expansion in C9ORF72 is the cause of chromosome 9p21-linked ALS-FTD

AE Renton, E Majounie, A Waite, J Simón-Sánchez… - Neuron, 2011 - cell.com
The chromosome 9p21 amyotrophic lateral sclerosis-frontotemporal dementia (ALS-FTD)
locus contains one of the last major unidentified autosomal-dominant genes underlying …

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

K Rascovsky, JR Hodges, D Knopman, MF Mendez… - Brain, 2011 - academic.oup.com
Based on the recent literature and collective experience, an international consortium
developed revised guidelines for the diagnosis of behavioural variant frontotemporal …

Mutations in the DJ-1 Gene Associated with Autosomal Recessive Early-Onset Parkinsonism

V Bonifati, P Rizzu, MJ Van Baren, O Schaap… - Science, 2003 - science.org
The DJ-1 gene encodes a ubiquitous, highly conserved protein. Here, we show that DJ-1
mutations are associated with PARK7, a monogenic form of human parkinsonism. The …

Clinical diagnosis of progressive supranuclear palsy: the movement disorder society criteria

GU Höglinger, G Respondek, M Stamelou… - Movement …, 2017 - Wiley Online Library
Background: PSP is a neuropathologically defined disease entity. Clinical diagnostic criteria,
published in 1996 by the National Institute of Neurological Disorders and Stroke/Society for …

Interobserver agreement for the assessment of handicap in stroke patients.

JC van Swieten, PJ Koudstaal, MC Visser… - stroke, 1988 - Am Heart Assoc
Interobserver agreement for the assessment of handicap in stroke patients was investigated
in a group of 10 senior neurologists and 24 residents from two centers. One hundred …

[HTML][HTML] Frequency of the C9orf72 hexanucleotide repeat expansion in patients with amyotrophic lateral sclerosis and frontotemporal dementia: a cross-sectional study

E Majounie, AE Renton, K Mok, EGP Dopper… - The Lancet …, 2012 - thelancet.com
Background We aimed to accurately estimate the frequency of a hexanucleotide repeat
expansion in C9orf72 that has been associated with a large proportion of cases of …

Dietary intake of antioxidants and risk of Alzheimer disease

MJ Engelhart, MI Geerlings, A Ruitenberg… - Jama, 2002 - jamanetwork.com
ContextLaboratory findings have suggested that oxidative stress may contribute to the
pathogenesis of Alzheimer disease. Therefore, the risk of Alzheimer disease might be …