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Beyond the Blue Economy: Creative Industries and Sustainable Development in Small Island Developing States

Rudge, Peter

1, 2021

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Sleep symptomatology in the National prion monitoring cohort

Journal of neurology, neurosurgery and psychiatry, 2023-11, Vol.94 (Suppl 1), p.A1-A2

2023

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Detection of prion infection in variant Creutzfeldt-Jakob disease: a blood-based assay

The Lancet (British edition), 2011-02, Vol.377 (9764), p.487-493

2011

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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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The language disorder of prion disease is characteristic of a dynamic aphasia and is rarely an isolated clinical feature

PloS one, 2018-01, Vol.13 (1), p.e0190818-e0190818

2018

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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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Variant CJD in an individual heterozygous for PRNP codon 129

The Lancet (British edition), 2009-12, Vol.374 (9707), p.2128-2128

2009

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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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Recollection and familiarity in dense hippocampal amnesia: A case study

Neuropsychologia, 2006, Vol.44 (3), p.489-506

2006

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CJD mimics and chameleons

Practical Neurology, 2017-04, Vol.17 (2), p.113-121

2017

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Predictive testing for inherited prion disease: report of 22 years experience

European journal of human genetics : EJHG, 2014-12, Vol.22 (12), p.1351-1356

2014

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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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Zidovudine plus lamivudine in Human T-Lymphotropic Virus type-I-associated myelopathy: a randomised trial

Retrovirology, 2006-09, Vol.3 (1), p.63-63, Article 63

2006

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Neuroanatomical correlates of prion disease progression - a 3T longitudinal voxel-based morphometry study

NeuroImage clinical, 2017-01, Vol.13 (C), p.89-96

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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Evidence for human transmission of amyloid-β pathology and cerebral amyloid angiopathy

Nature (London), 2015-09, Vol.525 (7568), p.247-250

2015

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Transmission of amyloid-β protein pathology from cadaveric pituitary growth hormone

Nature (London), 2018-12, Vol.564 (7736), p.415-419

2018

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Estimation of the number of inherited prion disease mutation carriers in the UK

European journal of human genetics : EJHG, 2022-10, Vol.30 (10), p.1167-1170

2022

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Iatrogenic Alzheimer's disease in recipients of cadaveric pituitary-derived growth hormone

Nature medicine, 2024-02, Vol.30 (2), p.394-402

2024

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Assessing initial MRI reports for suspected CJD patients

Journal of neurology, 2022-08, Vol.269 (8), p.4452-4458

2022

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Are multiplication facts implemented by the left supramarginal and angular gyri?

Neuropsychologia, 2002, Vol.40 (11), p.1786-1793

2002

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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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Beyond the Blue Economy: Creative Industries and Sustainable Development in Small Island Developing States

Sleep symptomatology in the National prion monitoring cohort

Detection of prion infection in variant Creutzfeldt-Jakob disease: a blood-based assay

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

The language disorder of prion disease is characteristic of a dynamic aphasia and is rarely an isolated clinical feature

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

Variant CJD in an individual heterozygous for PRNP codon 129

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

Recollection and familiarity in dense hippocampal amnesia: A case study

CJD mimics and chameleons

Predictive testing for inherited prion disease: report of 22 years experience

Imaging and CSF analyses effectively distinguish CJD from its mimics

Zidovudine plus lamivudine in Human T-Lymphotropic Virus type-I-associated myelopathy: a randomised trial

Neuroanatomical correlates of prion disease progression - a 3T longitudinal voxel-based morphometry study

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

Evidence for human transmission of amyloid-β pathology and cerebral amyloid angiopathy

Transmission of amyloid-β protein pathology from cadaveric pituitary growth hormone

Estimation of the number of inherited prion disease mutation carriers in the UK

Iatrogenic Alzheimer's disease in recipients of cadaveric pituitary-derived growth hormone

Assessing initial MRI reports for suspected CJD patients

Are multiplication facts implemented by the left supramarginal and angular gyri?

Cognitive decline heralds onset of symptomatic inherited prion disease

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