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Knowledge of famous faces and names in semantic dementia

Brain (London, England : 1878), 2004-04, Vol.127 (4), p.860-872

2004

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The role of lysosomes and autophagosomes in frontotemporal lobar degeneration

Neuropathology and applied neurobiology, 2019-04, Vol.45 (3), p.244-261

2019

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Emotion recognition in Huntington's disease and frontotemporal dementia

Neuropsychologia, 2008-09, Vol.46 (11), p.2638-2649

2008

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Progranulin gene mutations associated with frontotemporal dementia and progressive non-fluent aphasia

Brain (London, England : 1878), 2006-11, Vol.129 (11), p.3091-3102

2006

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Distinct behavioural profiles in frontotemporal dementia and semantic dementia

Journal of neurology, neurosurgery and psychiatry, 2001-03, Vol.70 (3), p.323-332

2001

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Frontotemporal lobar degeneration: a consensus on clinical diagnostic criteria

Neurology, 1998-12, Vol.51 (6), p.1546-1554

1998

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Qualitative neuropsychological performance characteristics in frontotemporal dementia and Alzheimer’s disease

Journal of neurology, neurosurgery and psychiatry, 2005-07, Vol.76 (7), p.920-927

2005

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Accuracy of single-photon emission computed tomography in differentiating frontotemporal dementia from Alzheimer’s disease

Journal of neurology, neurosurgery and psychiatry, 2007-04, Vol.78 (4), p.350-355

2007

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Evaluation of the NINCDS-ADRDA criteria in the differentiation of Alzheimer’s disease and frontotemporal dementia

Journal of neurology, neurosurgery and psychiatry, 1999-02, Vol.66 (2), p.184-188

1999

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Behaviour in frontotemporal dementia, Alzheimer's disease and vascular dementia

Acta neurologica Scandinavica, 2001-06, Vol.103 (6), p.367-378

2001

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Cognitive change in motor neurone disease/amyotrophic lateral sclerosis (MND/ALS)

Journal of the Neurological Sciences, 2000-11, Vol.180 (1), p.15-20

2000

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Arithmetic knowledge in semantic dementia: Is it invariably preserved?

Neuropsychologia, 2008-09, Vol.46 (11), p.2732-2744

2008

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Social cognition in frontotemporal dementia and Huntington’s disease

Neuropsychologia, 2003, Vol.41 (6), p.688-701

2003

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Foreign accent syndrome as the initial sign of primary progressive aphasia

Journal of neurology, neurosurgery and psychiatry, 2008-01, Vol.79 (1), p.79-81

2008

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Imbalance of a serotonergic system in frontotemporal dementia: implication for pharmacotherapy

Psychopharmacologia, 2008-03, Vol.196 (4), p.603-610

2008

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Diagnostic patterns of regional atrophy on MRI and regional cerebral blood flow change on SPECT in young onset patients with Alzheimer's disease, frontotemporal dementia and vascular dementia

Acta neurologica Scandinavica, 2002-04, Vol.105 (4), p.261-269

2002

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Nuclear carrier and RNA-binding proteins in frontotemporal lobar degeneration associated with fused in sarcoma (FUS) pathological changes

Neuropathology and applied neurobiology, 2013-02, Vol.39 (2), p.157-165

2013

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Frontotemporal dementia with Pick‐type histology associated with Q336R mutation in the tau gene

Brain (London, England : 1878), 2004-06, Vol.127 (6), p.1415-1426

2004

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Psychomotor, Executive, and Memory Function in Preclinical Huntington's Disease

Journal of clinical and experimental neuropsychology, 2002-04, Vol.24 (2), p.133-145

2002

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Inferring thought and action in motor neurone disease

Neuropsychologia, 2007-01, Vol.45 (6), p.1196-1207

2007

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Inherited frontotemporal dementia in nine british families associated with intronic mutations in the tau gene

Brain (London, England : 1878), 2002-04, Vol.125 (Pt 4), p.732-751

2002

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Psychiatric disorders in preclinical Huntington’s disease

Journal of neurology, neurosurgery and psychiatry, 2007-09, Vol.78 (9), p.939-943

2007

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Genetic associations between cathepsin D exon 2 C→T polymorphism and Alzheimer’s disease, and pathological correlations with genotype

Journal of neurology, neurosurgery and psychiatry, 2006-04, Vol.77 (4), p.515-517

2006

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Neurodegeneration in frontotemporal lobar degeneration and motor neurone disease associated with expansions in C9orf72 is linked to TDP-43 pathology and not associated with aggregated forms of dipeptide repeat proteins

Neuropathology and applied neurobiology, 2016-04, Vol.42 (3), p.242-254

2016

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Autopsy proven sporadic frontotemporal dementia due to microvacuolar-type histology, with onset at 21 years of age

Journal of neurology, neurosurgery and psychiatry, 2004-09, Vol.75 (9), p.1337-1339

2004

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Knowledge of famous faces and names in semantic dementia

The role of lysosomes and autophagosomes in frontotemporal lobar degeneration

Emotion recognition in Huntington's disease and frontotemporal dementia

Progranulin gene mutations associated with frontotemporal dementia and progressive non-fluent aphasia

Distinct behavioural profiles in frontotemporal dementia and semantic dementia

Frontotemporal lobar degeneration: a consensus on clinical diagnostic criteria

Qualitative neuropsychological performance characteristics in frontotemporal dementia and Alzheimer’s disease

Accuracy of single-photon emission computed tomography in differentiating frontotemporal dementia from Alzheimer’s disease

Evaluation of the NINCDS-ADRDA criteria in the differentiation of Alzheimer’s disease and frontotemporal dementia

Behaviour in frontotemporal dementia, Alzheimer's disease and vascular dementia

Cognitive change in motor neurone disease/amyotrophic lateral sclerosis (MND/ALS)

Arithmetic knowledge in semantic dementia: Is it invariably preserved?

Social cognition in frontotemporal dementia and Huntington’s disease

Foreign accent syndrome as the initial sign of primary progressive aphasia

Imbalance of a serotonergic system in frontotemporal dementia: implication for pharmacotherapy

Diagnostic patterns of regional atrophy on MRI and regional cerebral blood flow change on SPECT in young onset patients with Alzheimer's disease, frontotemporal dementia and vascular dementia

Nuclear carrier and RNA-binding proteins in frontotemporal lobar degeneration associated with fused in sarcoma (FUS) pathological changes

Frontotemporal dementia with Pick‐type histology associated with Q336R mutation in the tau gene

Psychomotor, Executive, and Memory Function in Preclinical Huntington's Disease

Inferring thought and action in motor neurone disease

Inherited frontotemporal dementia in nine british families associated with intronic mutations in the tau gene

Psychiatric disorders in preclinical Huntington’s disease

Genetic associations between cathepsin D exon 2 C→T polymorphism and Alzheimer’s disease, and pathological correlations with genotype

Neurodegeneration in frontotemporal lobar degeneration and motor neurone disease associated with expansions in C9orf72 is linked to TDP-43 pathology and not associated with aggregated forms of dipeptide repeat proteins

Autopsy proven sporadic frontotemporal dementia due to microvacuolar-type histology, with onset at 21 years of age

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