The case of a 48 year-old woman with bizarre and complex delusions.

PubWeight™: 0.89‹?›

🔗 View Article (PMID 20212429)

Published in Nat Rev Neurol on March 01, 2010

Authors

Clement T Loy1, Jillian J Kril, Julian N Trollor, Matthew C Kiernan, John B J Kwok, Steve Vucic, Glenda M Halliday, John R Hodges

Author Affiliations

1: Prince of Wales Medical Research Institute, Barker Street, Randwick, Sydney, NSW 2031, Australia.

Articles cited by this

Frontotemporal lobar degeneration: a consensus on clinical diagnostic criteria. Neurology (1998) 26.77

Familial amyotrophic lateral sclerosis with frontotemporal dementia is linked to a locus on chromosome 9p13.2-21.3. Brain (2006) 5.36

The Addenbrooke's Cognitive Examination Revised (ACE-R): a brief cognitive test battery for dementia screening. Int J Geriatr Psychiatry (2006) 4.73

Age of onset of mental disorders: a review of recent literature. Curr Opin Psychiatry (2007) 4.46

A new subtype of frontotemporal lobar degeneration with FUS pathology. Brain (2009) 4.40

Clinicopathological correlates in frontotemporal dementia. Ann Neurol (2004) 4.38

Pedigree with frontotemporal lobar degeneration--motor neuron disease and Tar DNA binding protein-43 positive neuropathology: genetic linkage to chromosome 9. BMC Neurol (2008) 2.34

Cortical hyperexcitability may precede the onset of familial amyotrophic lateral sclerosis. Brain (2008) 1.94

Development of methodology for conducting clinical trials in frontotemporal lobar degeneration. Brain (2008) 1.82

Selective impairment of verb processing associated with pathological changes in Brodmann areas 44 and 45 in the motor neurone disease-dementia-aphasia syndrome. Brain (2001) 1.78

A systematic review of neurotransmitter deficits and treatments in frontotemporal dementia. Neurology (2006) 1.62

Frontotemporal dementia presenting as schizophrenia-like psychosis in young people: clinicopathological series and review of cases. Br J Psychiatry (2009) 1.55

Progranulin mutations and amyotrophic lateral sclerosis or amyotrophic lateral sclerosis-frontotemporal dementia phenotypes. J Neurol Neurosurg Psychiatry (2007) 1.28

Time course of regional brain activation associated with onset of auditory/verbal hallucinations. Br J Psychiatry (2008) 1.24

Nature and course of cognitive function in late-life schizophrenia: a systematic review. Schizophr Res (2008) 1.17

Delusions in frontotemporal lobar degeneration. J Neurol (2009) 1.14

A comprehensive assessment of gray and white matter volumes and their relationship to outcome and severity in schizophrenia. Neuroimage (2007) 1.09

Distribution of brain atrophy in behavioral variant frontotemporal dementia. J Neurol Sci (2005) 1.02

Articles by these authors

Sensitivity of revised diagnostic criteria for the behavioural variant of frontotemporal dementia. Brain (2011) 9.90

Amyotrophic lateral sclerosis. Lancet (2011) 5.86

The Sydney multicenter study of Parkinson's disease: the inevitability of dementia at 20 years. Mov Disord (2008) 5.72

Common variants at 7p21 are associated with frontotemporal lobar degeneration with TDP-43 inclusions. Nat Genet (2010) 5.52

The Addenbrooke's Cognitive Examination Revised (ACE-R): a brief cognitive test battery for dementia screening. Int J Geriatr Psychiatry (2006) 4.73

Analysis of immune-related loci identifies 48 new susceptibility variants for multiple sclerosis. Nat Genet (2013) 4.62

Clinicopathological correlates in frontotemporal dementia. Ann Neurol (2004) 4.38

Clinical and pathological characterization of progressive aphasia. Ann Neurol (2006) 4.37

Mutations in the endosomal ESCRTIII-complex subunit CHMP2B in frontotemporal dementia. Nat Genet (2005) 4.21

Structure and deterioration of semantic memory: a neuropsychological and computational investigation. Psychol Rev (2004) 3.32

The pathological basis of semantic dementia. Brain (2005) 2.96

Hyperphagia, severe obesity, impaired cognitive function, and hyperactivity associated with functional loss of one copy of the brain-derived neurotrophic factor (BDNF) gene. Diabetes (2006) 2.87

Reduced glucocerebrosidase is associated with increased α-synuclein in sporadic Parkinson's disease. Brain (2014) 2.74

Neuropathological assessment of Parkinson's disease: refining the diagnostic criteria. Lancet Neurol (2009) 2.60

Controversies and priorities in amyotrophic lateral sclerosis. Lancet Neurol (2013) 2.52

Guillain-Barré syndrome: an update. J Clin Neurosci (2009) 2.46

Diagnostic criteria for the behavioral variant of frontotemporal dementia (bvFTD): current limitations and future directions. Alzheimer Dis Assoc Disord (2007) 2.43

The syndrome of transient epileptic amnesia. Ann Neurol (2007) 2.37

The effects of very early Alzheimer's disease on the characteristics of writing by a renowned author. Brain (2004) 2.34

Pedigree with frontotemporal lobar degeneration--motor neuron disease and Tar DNA binding protein-43 positive neuropathology: genetic linkage to chromosome 9. BMC Neurol (2008) 2.34

FUS pathology defines the majority of tau- and TDP-43-negative frontotemporal lobar degeneration. Acta Neuropathol (2010) 2.30

Neuropathologic correlates of white matter hyperintensities. Neurology (2008) 2.29

Limbic hypometabolism in Alzheimer's disease and mild cognitive impairment. Ann Neurol (2003) 2.26

Progressive non-fluent aphasia is associated with hypometabolism centred on the left anterior insula. Brain (2003) 2.25

Biomarkers in amyotrophic lateral sclerosis. Lancet Neurol (2009) 2.20

Specialization in the medial temporal lobe for processing of objects and scenes. Hippocampus (2005) 2.17

Theory of mind in patients with frontal variant frontotemporal dementia and Alzheimer's disease: theoretical and practical implications. Brain (2002) 2.17

Neuropathological background of phenotypical variability in frontotemporal dementia. Acta Neuropathol (2011) 2.17

GSK3B polymorphisms alter transcription and splicing in Parkinson's disease. Ann Neurol (2005) 2.14

Disease duration and the integrity of the nigrostriatal system in Parkinson's disease. Brain (2013) 2.09

Clinical diagnosis and management of amyotrophic lateral sclerosis. Nat Rev Neurol (2011) 2.08

Botulinum toxin modulates cortical maladaptation in post-stroke spasticity. Muscle Nerve (2013) 2.00

Frontotemporal dementia and motor neurone disease: overlapping clinic-pathological disorders. J Clin Neurosci (2009) 1.99

Advances in the early detection of Alzheimer's disease. Nat Med (2004) 1.97

Cortical hyperexcitability may precede the onset of familial amyotrophic lateral sclerosis. Brain (2008) 1.94

Subtypes of progressive aphasia: application of the International Consensus Criteria and validation using β-amyloid imaging. Brain (2011) 1.92

The ENIGMA Consortium: large-scale collaborative analyses of neuroimaging and genetic data. Brain Imaging Behav (2014) 1.90

What the left and right anterior fusiform gyri tell us about semantic memory. Brain (2010) 1.87

Perceptual deficits in amnesia: challenging the medial temporal lobe 'mnemonic' view. Neuropsychologia (2005) 1.83

An international consensus study of neuroleptic malignant syndrome diagnostic criteria using the Delphi method. J Clin Psychiatry (2011) 1.80

Multiple biological pathways link cognitive lifestyle to protection from dementia. Biol Psychiatry (2011) 1.79

Behavioural-variant frontotemporal dementia: diagnosis, clinical staging, and management. Lancet Neurol (2010) 1.79

Language function and dysfunction in corticobasal degeneration. Neurology (2003) 1.78

Left/right asymmetry of atrophy in semantic dementia: behavioral-cognitive implications. Neurology (2003) 1.76

Isolated bulbar phenotype of amyotrophic lateral sclerosis. Amyotroph Lateral Scler (2011) 1.75

The multiple sclerosis whole blood mRNA transcriptome and genetic associations indicate dysregulation of specific T cell pathways in pathogenesis. Hum Mol Genet (2010) 1.73

In vivo identification of human cortical areas using high-resolution MRI: an approach to cerebral structure-function correlation. Proc Natl Acad Sci U S A (2003) 1.72

Time to redefine PD? Introductory statement of the MDS Task Force on the definition of Parkinson's disease. Mov Disord (2014) 1.63

Segmental facial anhidrosis and tonic pupils with preserved deep tendon reflexes: a novel autonomic neuropathy. J Neuroophthalmol (2005) 1.63

Cognitive, extrapyramidal, and magnetic resonance imaging predictors of functional impairment in nondemented older community dwellers: the Sydney Older Person Study. J Am Geriatr Soc (2006) 1.63

Diagnostic criteria for corticobasal syndrome: a comparative study. J Neurol Neurosurg Psychiatry (2011) 1.61

Cortical excitability distinguishes ALS from mimic disorders. Clin Neurophysiol (2011) 1.59

Declarative memory impairments in Alzheimer's disease and semantic dementia. Neuroimage (2005) 1.59

Neural correlates of semantic and behavioural deficits in frontotemporal dementia. Neuroimage (2004) 1.58

Naming of objects, faces and buildings in mild cognitive impairment. Cortex (2007) 1.58

Social reasoning, emotion and empathy in frontotemporal dementia. Neuropsychologia (2005) 1.57

A possible role for humoral immunity in the pathogenesis of Parkinson's disease. Brain (2005) 1.57

Small-vessel disease in patients with Parkinson's disease: a clinicopathological study. Mov Disord (2012) 1.56

Modulatory effects on axonal function after intravenous immunoglobulin therapy in chronic inflammatory demyelinating polyneuropathy. Arch Neurol (2011) 1.55

Cortical excitability testing distinguishes Kennedy's disease from amyotrophic lateral sclerosis. Clin Neurophysiol (2008) 1.54

Split-hand index for the diagnosis of amyotrophic lateral sclerosis. Clin Neurophysiol (2012) 1.52

Abnormalities of the fornix in mild cognitive impairment are related to episodic memory loss. J Alzheimers Dis (2012) 1.52

Oxaliplatin-induced neurotoxicity: changes in axonal excitability precede development of neuropathy. Brain (2009) 1.50

Changes in human sensory axonal excitability induced by an ischaemic insult. Clin Neurophysiol (2008) 1.49

Progressive axonal dysfunction and clinical impairment in amyotrophic lateral sclerosis. Clin Neurophysiol (2012) 1.49

Novel threshold tracking techniques suggest that cortical hyperexcitability is an early feature of motor neuron disease. Brain (2006) 1.47

Corticomotoneuronal function in asymptomatic SOD-1 mutation carriers. Clin Neurophysiol (2010) 1.47

Progression in frontotemporal dementia: identifying a benign behavioral variant by magnetic resonance imaging. Arch Neurol (2006) 1.47

Validation of the Addenbrooke's Cognitive Examination III in frontotemporal dementia and Alzheimer's disease. Dement Geriatr Cogn Disord (2013) 1.47

Argyrophilic staining of nucleolar organizer region count and morphometry in benign and malignant melanocytic lesions. Am J Dermatopathol (2003) 1.44

Variability in neuronal expression of dopamine receptors and transporters in the substantia nigra. Mov Disord (2013) 1.44

C9ORF72 repeat expansion in clinical and neuropathologic frontotemporal dementia cohorts. Neurology (2012) 1.44

FUS mutations in amyotrophic lateral sclerosis: clinical, pathological, neurophysiological and genetic analysis. J Neurol Neurosurg Psychiatry (2009) 1.44

Detecting dementia: novel neuropsychological markers of preclinical Alzheimer's disease. Dement Geriatr Cogn Disord (2003) 1.43

P25alpha immunoreactive but alpha-synuclein immunonegative neuronal inclusions in multiple system atrophy. Acta Neuropathol (2006) 1.43

Mutations in progranulin explain atypical phenotypes with variants in MAPT. Brain (2006) 1.43

Riluzole: a glimmer of hope in the treatment of motor neurone disease. Med J Aust (2005) 1.42

Prevalence and predictors of “subjective cognitive complaints” in the Sydney Memory and Ageing Study. Am J Geriatr Psychiatry (2010) 1.41

Regional differences in ulnar nerve excitability may predispose to the development of entrapment neuropathy. Clin Neurophysiol (2010) 1.41