Browse by UCL people
Group by: Type | Date
Number of items: 11.
2021
Koriath, CAM;
Kenny, J;
Ryan, NS;
Rohrer, JD;
Schott, JM;
Houlden, H;
Fox, NC;
... Mead, S; + view all
(2021)
Genetic testing in dementia — utility and clinical strategies.
Nature Reviews Neurology
, 17
pp. 23-36.
10.1038/s41582-020-00416-1.
|
|
O'Connor, A;
Abel, E;
Fraser, MR;
Ryan, NS;
Jiménez, DA;
Koriath, C;
Chávez-Gutiérrez, L;
... Fox, NC; + view all
(2021)
A novel presenilin 1 duplication mutation (Ile168dup) causing Alzheimer's disease associated with myoclonus, seizures and pyramidal features.
Neurobiology of Aging
, 103
137.e1-137.e5.
10.1016/j.neurobiolaging.2021.01.032.
|
2020
|
Koriath, Carolin Anna Maria;
(2020)
Next‐generation sequencing in the diagnosis of Dementia and Huntington’s disease Phenocopy Syndromes.
Doctoral thesis (Ph.D), UCL (University College London).
|
 |
2019
|
Convery, RS;
Jiao, J;
Clarke, MTM;
Moore, KM;
Koriath, CAM;
Woollacott, IOC;
Weston, PSJ;
... Rohrer, JD; + view all
(2019)
Longitudinal (¹⁸F)AV-1451 PET imaging in a patient with frontotemporal dementia due to a Q351R MAPT mutation.
Journal of Neurology, Neurosurgery & Psychiatry
10.1136/jnnp-2019-320904.
(In press).
|
|
Koriath, C;
Lashley, T;
Taylor, W;
Druyeh, R;
Dimitriadis, A;
Denning, N;
Williams, J;
... Mead, S; + view all
(2019)
ApoE4 lowers age at onset in patients with frontotemporal dementia and tauopathy independent of amyloid-β copathology.
Alzheimer's and Dementia: Diagnosis, Assessment and Disease Monitoring
, 11
pp. 277-280.
10.1016/j.dadm.2019.01.010.
|
|
|
Thaler, FS;
Koriath, C;
Vollmar, C;
Bardins, S;
Kremmyda, O;
Danek, A;
(2019)
Acute frontal eye field infarction: A topodiagnostic challenge.
Neurology
, 92
(4)
pp. 193-195.
10.1212/WNL.0000000000006813.
|
2018
|
Jaunmuktane, Z;
Quaegebeur, A;
Taipa, R;
Viana-Baptista, M;
Barbosa, R;
Koriath, C;
Sciot, R;
... Brandner, S; + view all
(2018)
Evidence of amyloid-β cerebral amyloid angiopathy transmission through neurosurgery.
Acta Neuropathologica
, 135
(5)
pp. 671-679.
10.1007/s00401-018-1822-2.
|
|
|
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).
|
|
|
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.
|
|
2017
|
Kenny, J;
Woollacott, I;
Koriath, C;
Hosszu, L;
Adamson, G;
Rudge, P;
Rossor, MN;
... Mead, S; + view all
(2017)
A novel prion protein variant in a patient with semantic dementia.
[Letter].
Journal of Neurology Neurosurgery and Psychiatry
, 2017
(88)
pp. 890-892.
10.1136/jnnp-2017-315577.
|
|
2016
|
Koriath, CAM;
Bocchetta, M;
Brotherhood, E;
Woollacott, I;
Norsworthy, P;
Simon-Sanchez, J;
Blauwendraat, C;
... Rohrer, J; + view all
(2016)
The clinical, neuroanatomical, and neuropathologic phenotype of TBK1-associated frontotemporal dementia: A longitudinal case report.
Alzheimer's and Dementia
, 6
pp. 75-81.
10.1016/j.dadm.2016.10.003.
|
|
