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

…, YAL Pijnenburg, NC Fox, JC Van Swieten - 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 …

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

…, M Troiano, MR Turner, JC van Swieten… - 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 …

Recommendations to distinguish behavioural variant frontotemporal dementia from psychiatric disorders

…, J Van Swieten, M Hornberger, H Rosen, J Hodges… - Brain, 2020 - academic.oup.com
The behavioural variant of frontotemporal dementia (bvFTD) is a frequent cause of early-onset
dementia. The diagnosis of bvFTD remains challenging because of the limited accuracy …

Interobserver agreement for the assessment of handicap in stroke patients.

JC van Swieten, PJ Koudstaal, MC Visser… - stroke, 1988 - Am Heart Assoc
… Rankin J: Cerebral vascular accidents in patients over the age of 60. 2. Prognosis. … M,
Teasdale GM, van Crevel H, van Gijn J: Antifibrinorytic treatment in subarachnoid hemorrhage. …

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

…, F Owen, BA Oostra, J Hardy, A Goate, J van Swieten… - Nature, 1998 - nature.com
Thirteen families have been described with an autosomal dominantly inherited dementia
named frontotemporal dementia and parkinsonism linked to chromosome 17 (FTDP-17) 1 , 2 , 3 …

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

…, JW van Dongen, N Vanacore, JC van Swieten… - 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 function …

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

…, JC Schymick, H Laaksovirta, JC Van Swieten… - 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 these …

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

…, JL Whitwell, J Levin, J van Swieten… - 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 …

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

…, MF Mendez, JH Kramer, J Neuhaus, JC Van Swieten… - 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 dementia. The …

Cerebral white matter lesions, vascular risk factors, and cognitive function in a population‐based study: the Rotterdam Study

MMB Breteler, JC Van Swieten, ML Bots, DE Grobbee… - Neurology, 1994 - AAN Enterprises
Cerebral white matter lesions are a common finding on MRI in elderly persons. We studied
the prevalence of white matter lesions and their relation with classic cardiovascular risk …