John Collinge, BSc, MB, ChB, MD, FRCP, FRS

Neurodegenerative Diseases University College London, London, United Kingdom 
"John Collinge"

Cross-listing: Neurotree - Neuropathology Tree

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Kenny J, Woollacott I, Koriath C, et al. (2017) A novel prion protein variant in a patient with semantic dementia. Journal of Neurology, Neurosurgery, and Psychiatry
Mok T, Jaunmuktane Z, Joiner S, et al. (2017) Variant Creutzfeldt-Jakob Disease in a Patient with Heterozygosity at PRNP Codon 129. The New England Journal of Medicine. 376: 292-294
Luk C, Jones S, Thomas C, et al. (2016) Diagnosing Sporadic Creutzfeldt-Jakob Disease by the Detection of Abnormal Prion Protein in Patient Urine. Jama Neurology
Collinge J, Jaunmuktane Z, Mead S, et al. (2016) Collinge et al. reply. Nature. 537: E7-9
Franko E, Wehner T, Joly O, et al. (2016) Quantitative EEG parameters correlate with the progression of human prion diseases. Journal of Neurology, Neurosurgery, and Psychiatry
Collinge J, Jaunmuktane Z, Mead S, et al. (2016) Collinge et al. reply. Nature. 535: E2-3
Properzi F, Badhan A, Klier S, et al. (2016) Physical, chemical and kinetic factors affecting prion infectivity. Prion. 0
Terry C, Wenborn A, Gros N, et al. (2016) Ex vivo mammalian prions are formed of paired double helical prion protein fibrils. Open Biology. 6
Balendra R, Uphill J, Collinson C, et al. (2016) Variants of PLCXD3 are not associated with variant or sporadic Creutzfeldt-Jakob disease in a large international study. Bmc Medical Genetics. 17: 28
Schott JM, Crutch SJ, Carrasquillo MM, et al. (2016) Genetic risk factors for the posterior cortical atrophy variant of Alzheimer's disease. Alzheimer's & Dementia : the Journal of the Alzheimer's Association
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