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Hypokinesia without decrement distinguishes progressive supranuclear palsy from Parkinson's disease

Brain (London, England : 1878), 2012-04, Vol.135 (Pt 4), p.1141-1153

2012

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Does corticobasal degeneration exist? A clinicopathological re-evaluation

Brain (London, England : 1878), 2010-07, Vol.133 (7), p.2045-2057

2010

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Conventional magnetic resonance imaging in confirmed progressive supranuclear palsy and multiple system atrophy

Movement disorders, 2012-12, Vol.27 (14), p.1754-1762

2012

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Nonmotor symptoms as presenting complaints in Parkinson's disease: A clinicopathological study

Movement disorders, 2008-01, Vol.23 (1), p.101-106

2008

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The midbrain to pons ratio: a simple and specific MRI sign of progressive supranuclear palsy

Neurology, 2013-05, Vol.80 (20), p.1856-1861

2013

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The genetic and clinico‐pathological profile of early‐onset progressive supranuclear palsy

Movement disorders, 2019-09, Vol.34 (9), p.1307-1314

2019

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278 Inspector norse

Journal of neurology, neurosurgery and psychiatry, 2018-10, Vol.89 (10), p.A41-A41

2018

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MM2 subtype of sporadic Creutzfeldt-Jakob disease may underlie the clinical presentation of progressive supranuclear palsy

Journal of neurology, 2013-04, Vol.260 (4), p.1031-1036

2013

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Targeting of the pedunculopontine nucleus by an MRI-guided approach: a cadaver study

Journal of Neural Transmission, 2011-10, Vol.118 (10), p.1487-1495

2011

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Compulsive versifying after treatment of transient epileptic amnesia

Neurocase, 2015-09, Vol.21 (5), p.548-553

2015

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Neurofilament light levels predict clinical progression and death in multiple system atrophy

Brain (London, England : 1878), 2022-12, Vol.145 (12), p.4398-4408

2022

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Specialist physiotherapy for functional motor disorder in England and Scotland (Physio4FMD): a pragmatic, multicentre, phase 3 randomised controlled trial

Lancet neurology, 2024-07, Vol.23 (7), p.675-686

2024

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Physio4FMD: protocol for a multicentre randomised controlled trial of specialist physiotherapy for functional motor disorder

BMC neurology, 2019-10, Vol.19 (1), p.242-242, Article 242

2019

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Parkinson’s disease with Onuf’s nucleus involvement mimicking multiple system atrophy

BMJ case reports, 2009, Vol.2009 (jan27 1), p.bcr0820080774-bcr0820080774

2009

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The unfolded protein response is activated in disease-affected brain regions in progressive supranuclear palsy and Alzheimer's disease

Acta neuropathologica communications, 2013-07, Vol.1 (1), p.31-31, Article 31

2013

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SEE NO EVIL, HEAR NO EVIL, SPEAK NO EVIL… KEEP IT A SICRET

Journal of neurology, neurosurgery and psychiatry, 2014-10, Vol.85 (10), p.e4.142-e4

2014

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Deep brain stimulation of the subthalamic nucleus: histological verification and 9.4-T MRI correlation

Acta neurochirurgica, 2015-12, Vol.157 (12), p.2143-2147

2015

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COMPULSIVE VERSIFYING IN TRANSIENT EPILEPTIC AMNESIA

Journal of neurology, neurosurgery and psychiatry, 2014-10, Vol.85 (10), p.e4.193-e4

2014

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Improving Conversations about Parkinson's Dementia

Movement disorders clinical practice (Hoboken, N.J.), 2024-07, Vol.11 (7), p.814-824

2024

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Kjellin syndrome: hereditary spastic paraplegia with pathognomonic macular appearance

Practical neurology, 2014-08, Vol.14 (4), p.278-279

2014

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Concomitant progressive supranuclear palsy and multiple system atrophy: More than a simple twist of fate?

Neuroscience letters, 2009-12, Vol.467 (3), p.208-211

2009

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Evidence for pre and postsynaptic nigrostriatal dysfunction in the fragile X tremor-Ataxia syndrome

Movement disorders, 2009-06, Vol.24 (8), p.1245-1247

2009

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Neurodegeneration: Cerebellum and Brain Stem

Imaging of the Brain, 2013, p.948-948

2013

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Evidence for pre and postsynaptic nigrostriatal dysfunction in the fragile X tremor-ataxia syndrome

Movement disorders : official journal of the Movement Disorder Society, 2009, Vol.24 (8), p.1245-1247

2009

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Hypokinesia without decrement distinguishes progressive supranuclear palsy from Parkinson's disease

Does corticobasal degeneration exist? A clinicopathological re-evaluation

Conventional magnetic resonance imaging in confirmed progressive supranuclear palsy and multiple system atrophy

Nonmotor symptoms as presenting complaints in Parkinson's disease: A clinicopathological study

The midbrain to pons ratio: a simple and specific MRI sign of progressive supranuclear palsy

The genetic and clinico‐pathological profile of early‐onset progressive supranuclear palsy

278 Inspector norse

MM2 subtype of sporadic Creutzfeldt-Jakob disease may underlie the clinical presentation of progressive supranuclear palsy

Targeting of the pedunculopontine nucleus by an MRI-guided approach: a cadaver study

Compulsive versifying after treatment of transient epileptic amnesia

Neurofilament light levels predict clinical progression and death in multiple system atrophy

Identification of common variants influencing risk of the tauopathy progressive supranuclear palsy

Specialist physiotherapy for functional motor disorder in England and Scotland (Physio4FMD): a pragmatic, multicentre, phase 3 randomised controlled trial

Physio4FMD: protocol for a multicentre randomised controlled trial of specialist physiotherapy for functional motor disorder

Parkinson’s disease with Onuf’s nucleus involvement mimicking multiple system atrophy

The unfolded protein response is activated in disease-affected brain regions in progressive supranuclear palsy and Alzheimer's disease

SEE NO EVIL, HEAR NO EVIL, SPEAK NO EVIL… KEEP IT A SICRET

Deep brain stimulation of the subthalamic nucleus: histological verification and 9.4-T MRI correlation

COMPULSIVE VERSIFYING IN TRANSIENT EPILEPTIC AMNESIA

Improving Conversations about Parkinson's Dementia

Kjellin syndrome: hereditary spastic paraplegia with pathognomonic macular appearance

Concomitant progressive supranuclear palsy and multiple system atrophy: More than a simple twist of fate?

Evidence for pre and postsynaptic nigrostriatal dysfunction in the fragile X tremor-Ataxia syndrome

Neurodegeneration: Cerebellum and Brain Stem

Evidence for pre and postsynaptic nigrostriatal dysfunction in the fragile X tremor-ataxia syndrome

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