The cognitive profile of prion disease: a prospective clinical and imaging study-Reference-Cited by-同舟云学术

The cognitive profile of prion disease: a prospective clinical and imaging study

Published:2015-04-07 Issue:5 Volume:2 Page:548-558
ISSN:2328-9503
Container-title:Annals of Clinical and Translational Neurology
language:en
Short-container-title:Ann Clin Transl Neurol

Author:

Caine Diana¹²³,Tinelli Renata J.²,Hyare Harpreet¹³,De Vita Enrico⁴⁵,Lowe Jessica³,Lukic Ana¹³,Thompson Andrew¹³,Porter Marie-Claire¹³,Cipolotti Lisa²,Rudge Peter¹⁶,Collinge John¹⁶,Mead Simon¹⁶

Affiliation:

1. NHS National Prion Clinic; National Hospital for Neurology and Neurosurgery (NHNN); University College London Hospitals NHS Foundation Trust; London United Kingdom

2. Department of Neuropsychology; NHNN; University College London Hospitals NHS Foundation Trust; London United Kingdom

3. Department of Neurodegenerative Disease; UCL Institute of Neurology; London United Kingdom

4. Academic Neuroradiological Unit; Department of Brain Repair and Rehabilitation; UCL Institute of Neurology; London United Kingdom

5. Lysholm Department of Neuroradiology; NHNN; University College London Hospitals NHS Foundation Trust; London United Kingdom

6. MRC Prion Unit; Department of Neurodegenerative Disease; UCL Institute of Neurology; London United Kingdom

Funder

Department of Health

UCLH/UCL Biomedical Research Centre

Medical Research Council

Publisher

Wiley

Subject

Neurology (clinical),General Neuroscience

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/acn3.195/fullpdf

Reference51 articles.

1. First hundred cases of variant Creutzfeldt-Jakob disease: retrospective case note review of early psychiatric and neurological features;Spencer;BMJ,2002

2. Iatrogenic Creutzfeldt-Jakob disease at the millennium;Brown;Neurology,2000

3. Early cognitive decline in Creutzfeldt-Jakob disease associated with human growth hormone treatment;Cordery;J Neurol Neurosurg Psychiatry,2003

4. Linkage of a prion protein missense variant to Gerstmann-Straussler syndrome;Hsiao;Nature,1989

5. Phenotypic heterogeneity and genetic modification of P102L inherited prion disease in an international series;Webb;Brain,2008

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