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Imaging and CSF analyses effectively distinguish CJD from its mimics

Journal of neurology, neurosurgery and psychiatry, 2018-05, Vol.89 (5), p.461-466

2018

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Safety and efficacy of quinacrine in human prion disease (PRION-1 study): a patient-preference trial

Lancet neurology, 2009-04, Vol.8 (4), p.334-344

2009

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Infratentorial superficial siderosis: Classification, diagnostic criteria, and rational investigation pathway

Annals of neurology, 2017-03, Vol.81 (3), p.333-343

2017

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Neuronal antibodies in patients with suspected or confirmed sporadic Creutzfeldt-Jakob disease

Journal of neurology, neurosurgery and psychiatry, 2015-06, Vol.86 (6), p.692-694

2015

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Prevalence and Treatments of Movement Disorders in Prion Diseases: A Longitudinal Cohort Study

Movement disorders, 2022-09, Vol.37 (9), p.1893-1903

2022

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Cognitive decline heralds onset of symptomatic inherited prion disease

Brain (London, England : 1878), 2021-04, Vol.144 (3), p.989-998

2021

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Early neurophysiological biomarkers and spinal cord pathology in inherited prion disease

Brain (London, England : 1878), 2019-03, Vol.142 (3), p.760-770

2019

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Iatrogenic cerebral amyloid angiopathy: an emerging clinical phenomenon

Journal of neurology, neurosurgery and psychiatry, 2022-07, Vol.93 (7), p.693-700

2022

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Transmissibility of Alzheimer’s? Evidence from recipients of human growth hormone

The Neuroscientist (Baltimore, Md.), 2024-08, Vol.30 (4), p.397-397

2024

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Clinical Trial Simulations Based on Genetic Stratification and the Natural History of a Functional Outcome Measure in Creutzfeldt-Jakob Disease

JAMA neurology, 2016-04, Vol.73 (4), p.447

2016

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The Medical Research Council Prion Disease Rating Scale: a new outcome measure for prion disease therapeutic trials developed and validated using systematic observational studies

Brain (London, England : 1878), 2013-04, Vol.136 (Pt 4), p.1116-1127

2013

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Iatrogenic CJD due to pituitary-derived growth hormone with genetically determined incubation times of up to 40 years

Brain (London, England : 1878), 2015-11, Vol.138 (Pt 11), p.3386-3399

2015

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High-b-Value Diffusion MR Imaging and Basal Nuclei Apparent Diffusion Coefficient Measurements in Variant and Sporadic Creutzfeldt-Jakob Disease

American journal of neuroradiology : AJNR, 2010-03, Vol.31 (3), p.521-526

2010

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Immunotherapy-responsive seizure-like episodes with potassium channel antibodies

Neurology, 2008-11, Vol.71 (20), p.1647-1648

2008

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Early neurophysiological biomarkers and spinal cord pathology in inherited prion disease

Brain (London, England : 1878), 2019-05, Vol.142 (5), p.e21-e21

2019

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MRI findings are often missed in the diagnosis of Creutzfeldt-Jakob disease

BMC neurology, 2012-12, Vol.12 (1), p.153-153, Article 153

2012

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Evolution of Diffusion-Weighted Magnetic Resonance Imaging Signal Abnormality in Sporadic Creutzfeldt-Jakob Disease, With Histopathological Correlation

JAMA neurology, 2016-01, Vol.73 (1), p.76

2016

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Development of novel clinical examination scales for the measurement of disease severity in Creutzfeldt-Jakob disease

Journal of neurology, neurosurgery and psychiatry, 2022-04, Vol.93 (4), p.404-412

2022

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Pelvic floor muscle training for women with lumbopelvic pain: A systematic review and meta‐analysis

European journal of pain, 2020-11, Vol.24 (10), p.1865-1879

2020

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Neurological complications in Behçet's syndrome

Brain (London, England : 1878), 1999-11, Vol.122 ( Pt 11) (11), p.2183-2183

1999

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Autoantibodies in sporadic Creutzfeldt-Jakob disease

JAMA neurology, 2013-07, Vol.70 (7), p.919

2013

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Quantitative EEG parameters correlate with the progression of human prion diseases

Journal of neurology, neurosurgery and psychiatry, 2016-10, Vol.87 (10), p.1061-1067

2016

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The inner ear and the neurologist

Journal of neurology, neurosurgery and psychiatry, 2007-02, Vol.78 (2), p.114-122

2007

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Visual vertigo: symptom assessment, spatial orientation and postural control

Brain (London, England : 1878), 2001-08, Vol.124 (8), p.1646-1656

2001

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Seed amplification and neurodegeneration marker trajectories in individuals at risk of prion disease

Brain (London, England : 1878), 2023-06, Vol.146 (6), p.2570-2583

2023

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Imaging and CSF analyses effectively distinguish CJD from its mimics

Safety and efficacy of quinacrine in human prion disease (PRION-1 study): a patient-preference trial

Infratentorial superficial siderosis: Classification, diagnostic criteria, and rational investigation pathway

Neuronal antibodies in patients with suspected or confirmed sporadic Creutzfeldt-Jakob disease

Prevalence and Treatments of Movement Disorders in Prion Diseases: A Longitudinal Cohort Study

Cognitive decline heralds onset of symptomatic inherited prion disease

Early neurophysiological biomarkers and spinal cord pathology in inherited prion disease

Iatrogenic cerebral amyloid angiopathy: an emerging clinical phenomenon

Transmissibility of Alzheimer’s? Evidence from recipients of human growth hormone

Clinical Trial Simulations Based on Genetic Stratification and the Natural History of a Functional Outcome Measure in Creutzfeldt-Jakob Disease

The Medical Research Council Prion Disease Rating Scale: a new outcome measure for prion disease therapeutic trials developed and validated using systematic observational studies

Iatrogenic CJD due to pituitary-derived growth hormone with genetically determined incubation times of up to 40 years

High-b-Value Diffusion MR Imaging and Basal Nuclei Apparent Diffusion Coefficient Measurements in Variant and Sporadic Creutzfeldt-Jakob Disease

Immunotherapy-responsive seizure-like episodes with potassium channel antibodies

Early neurophysiological biomarkers and spinal cord pathology in inherited prion disease

MRI findings are often missed in the diagnosis of Creutzfeldt-Jakob disease

Evolution of Diffusion-Weighted Magnetic Resonance Imaging Signal Abnormality in Sporadic Creutzfeldt-Jakob Disease, With Histopathological Correlation

Development of novel clinical examination scales for the measurement of disease severity in Creutzfeldt-Jakob disease

Pelvic floor muscle training for women with lumbopelvic pain: A systematic review and meta‐analysis

Neurological complications in Behçet's syndrome

Autoantibodies in sporadic Creutzfeldt-Jakob disease

Quantitative EEG parameters correlate with the progression of human prion diseases

The inner ear and the neurologist

Visual vertigo: symptom assessment, spatial orientation and postural control

Seed amplification and neurodegeneration marker trajectories in individuals at risk of prion disease

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