Browse by UCL people
Group by: Type | Date
Number of items: 16.
2023
Mok, Tze How;
(2023)
Defining the onset of prion infection and neurodegeneration in healthy individuals at risk of prion disease.
Doctoral thesis (M.D(Res)), UCL (University College London).
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2022
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Nihat, A;
Mok, TH;
Odd, H;
Thompson, AGB;
Caine, D;
McNiven, K;
O'Donnell, V;
... Mead, S; + view all
(2022)
Development of novel clinical examination scales for the measurement of disease severity in Creutzfeldt-Jakob disease.
Journal of Neurology, Neurosurgery & Psychiatry
10.1136/jnnp-2021-327722.
(In press).
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2021
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Brennecke, N;
Cali, I;
Mok, TH;
Speedy, H;
Consortium, GER;
Hosszu, LLP;
Stehmann, C;
... Appleby, BS; + view all
(2021)
Characterization of Prion Disease Associated with a Two-Octapeptide Repeat Insertion.
Viruses
, 13
(9)
, Article 1794. 10.3390/v13091794.
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Mengel, D;
Mok, TH;
Nihat, A;
Liu, W;
Rissman, RA;
Galasko, D;
Zetterberg, H;
... Walsh, DM; + view all
(2021)
NT1-Tau Is Increased in CSF and Plasma of CJD Patients, and Correlates with Disease Progression.
Cells
, 10
(12)
, Article 3514. 10.3390/cells10123514.
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Mok, TH;
Nihat, A;
Luk, C;
Sequeira, D;
Batchelor, M;
Mead, S;
Collinge, J;
(2021)
Bank vole prion protein extends the use of RT-QuIC assays to detect prions in a range of inherited prion diseases.
Scientific Reports
, 11
(1)
, Article 5231. 10.1038/s41598-021-84527-9.
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Mole, J;
Mead, S;
Rudge, P;
Nihat, A;
Mok, T;
Collinge, J;
Caine, D;
(2021)
Cognitive decline heralds onset of symptomatic inherited prion disease.
Brain
, 144
(3)
pp. 989-998.
10.1093/brain/awaa409.
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Thompson, AGB;
Anastasiadis, P;
Druyeh, R;
Whitworth, I;
Nayak, A;
Nihat, A;
Mok, TH;
... Mead, S; + view all
(2021)
Evaluation of plasma tau and neurofilament light chain biomarkers in a 12-year clinical cohort of human prion diseases.
Molecular Psychiatry
10.1038/s41380-021-01045-w.
(In press).
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2020
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Jones, E;
Hummerich, H;
Viré, E;
Uphill, J;
Dimitriadis, A;
Speedy, H;
Campbell, T;
... Mead, S; + view all
(2020)
Identification of novel risk loci and causal insights for sporadic Creutzfeldt-Jakob disease: a genome-wide association study.
The Lancet Neurology
, 19
(10)
pp. 840-848.
10.1016/S1474-4422(20)30273-8.
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Mok, TH;
Mead, S;
(2020)
Preclinical biomarkers of prion infection and neurodegeneration.
Current Opinion in Neurobiology
, 61
pp. 82-88.
10.1016/j.conb.2020.01.009.
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Norsworthy, PJ;
Thompson, AGB;
Mok, TH;
Guntoro, F;
Dabin, LC;
Nihat, A;
Paterson, RW;
... Viré, EA; + view all
(2020)
A blood miRNA signature associates with sporadic Creutzfeldt-Jakob disease diagnosis.
Nature Communications
, 11
(1)
, Article 3960. 10.1038/s41467-020-17655-x.
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2019
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Canas, LS;
Sudre, CH;
De Vita, E;
Nihat, A;
Mok, TH;
Slattery, CF;
Paterson, RW;
... Modat, M; + view all
(2019)
Prion disease diagnosis using subject-specific imaging biomarkers within a multi-kernel Gaussian process.
NeuroImage: Clinical
, Article 102051. 10.1016/j.nicl.2019.102051.
(In press).
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2018
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Koriath, C;
(2018)
Predictors for a dementia gene mutation based on gene-panel next-generation sequencing of a large dementia referral series.
Molecular Psychiatry
10.1038/s41380-018-0224-0.
(In press).
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Mok, TH;
Koriath, C;
Jaunmuktane, Z;
Campbell, T;
Joiner, S;
Wadsworth, JDF;
Hosszu, LLP;
... Mead, S; + view all
(2018)
Evaluating the causality of novel sequence variants in the prion protein gene by example.
Neurobiology of Aging
, 71
265.e1-265.e7.
10.1016/j.neurobiolaging.2018.05.011.
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2017
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Mok, T;
Jaunmuktane, Z;
Joiner, S;
Campbell, T;
Morgan, C;
Wakerley, B;
Golestani, F;
... Collinge, J; + view all
(2017)
Variant Creutzfeldt-Jakob Disease in a Patient with Heterozygosity at PRNP Codon 129.
The New England Journal of Medicine
, 376
(3)
pp. 292-294.
10.1056/NEJMc1610003.
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2016
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Luk, C;
Jones, S;
Thomas, C;
Fox, NC;
Mok, TH;
Mead, S;
Collinge, J;
(2016)
Diagnosing Sporadic Creutzfeldt-Jakob Disease by the Detection of Abnormal Prion Protein in Patient Urine.
JAMA Neurology
, 73
(12)
pp. 1454-1460.
10.1001/jamaneurol.2016.3733.
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Mead, S;
Burnell, M;
Lowe, J;
Thompson, A;
Lukic, A;
Porter, MC;
Carswell, C;
... Collinge, J; + view all
(2016)
Clinical Trial Simulations Based on Genetic Stratification and the Natural History of a Functional Outcome Measure in Creutzfeldt-Jakob Disease.
JAMA Neurology
, 73
(4)
pp. 447-455.
10.1001/jamaneurol.2015.4885.
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