Browse by UCL people
Group by: Type | Date
Number of items: 16.
Article
Kara, E;
Crimi, A;
Wiedmer, A;
Emmenegger, M;
Manzoni, C;
Bandres-Ciga, S;
D'Sa, K;
... Aguzzi, A; + view all
(2021)
An integrated genomic approach to dissect the genetic landscape regulating the cell-to-cell transfer of α-synuclein.
Cell Reports
, 35
(10)
, Article 109189. 10.1016/j.celrep.2021.109189.
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Kara, E;
Hardy, J;
Houlden, H;
(2013)
The pallidopyramidal syndromes: Nosology, aetiology and pathogenesis.
Current Opinion in Neurology
, 26
(4)
381 - 394.
10.1097/WCO.0b013e3283632e83.
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Kara, E;
Lewis, PA;
Ling, H;
Proukakis, C;
Houlden, H;
Hardy, J;
(2013)
α-Synuclein mutations cluster around a putative protein loop.
Neurosci Lett
, 546
67 - 70.
10.1016/j.neulet.2013.04.058.
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Kara, E;
Ling, H;
Pittman, AM;
Shaw, K;
de Silva, R;
Simone, R;
Holton, JL;
... Revesz, T; + view all
(2012)
The MAPT p.A152T variant is a risk factor associated with tauopathies with atypical clinical and neuropathological features.
Neurobioly of Aging
, 33
(9)
2231.e7 - 2231.e14.
10.1016/j.neurobiolaging.2012.04.006.
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Kara, E;
Tucci, A;
Manzoni, C;
Lynch, DS;
Elpidorou, M;
Bettencourt, C;
Chelban, V;
... Houlden, H; + view all
(2016)
Genetic and phenotypic characterization of complex hereditary spastic paraplegia.
Brain
, 139
(7)
pp. 1904-1918.
10.1093/brain/aww111.
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Kiely, AP;
Asi, YT;
Kara, E;
Limousin, P;
Ling, H;
Lewis, P;
Proukakis, C;
... Holton, JL; + view all
(2013)
α-Synucleinopathy associated with G51D SNCA mutation: a link between Parkinson's disease and multiple system atrophy?
Acta Neuropathologica
, 125
(5)
753 - 769.
10.1007/s00401-013-1096-7.
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Kiely, AP;
Ling, H;
Asi, YT;
Kara, E;
Proukakis, C;
Schapira, AH;
Morris, HR;
... Holton, JL; + view all
(2015)
Distinct clinical and neuropathological features of G51D SNCA mutation cases compared with SNCA duplication and H50Q mutation.
Molecular Neurodegeneration
, 10
, Article 41. 10.1186/s13024-015-0038-3.
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Ling, H;
Kara, E;
Bandopadhyay, R;
Hardy, J;
Holton, J;
Xiromerisiou, G;
Lees, A;
... Revesz, T; + view all
(2013)
TDP-43 pathology in a patient carrying G2019S LRRK2 mutation and a novel p.Q124E MAPT.
Neurobiol Aging
, 34
(12)
2889.e5 - 2889.e9.
10.1016/j.neurobiolaging.2013.04.011.
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Ling, H;
Kara, E;
Revesz, T;
Lees, AJ;
Plant, GT;
Martino, D;
Houlden, H;
... Holton, JL; + view all
(2014)
Concomitant progressive supranuclear palsy and chronic traumatic encephalopathy in a boxer.
Acta Neuropathol Commun
, 2
(1)
, Article 24. 10.1186/2051-5960-2-24.
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Mackenzie, Strachan;
Shafat, Manar;
Roddy, Harriet;
Hyare, Harpreet;
Neill, Lorna;
Marzolini, Maria AV;
Gilhooley, Michael;
... Roddie, Claire; + view all
(2021)
Pembrolizumab for the treatment of progressive multifocal leukoencephalopathy following anti-CD19 CAR-T therapy: a case report.
EJHaem
, 2
(4)
pp. 848-853.
10.1002/jha2.274.
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Manzoni, C;
Mamais, A;
Dihanich, S;
McGoldrick, P;
Devine, MJ;
Zerle, J;
Kara, E;
... Lewis, PA; + view all
(2013)
Pathogenic Parkinson's disease mutations across the functional domains of LRRK2 alter the autophagic/lysosomal response to starvation.
Biochemical and Biophysical Research Communications
, 441
(4)
pp. 862-866.
10.1016/j.bbrc.2013.10.159.
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Proukakis, C;
Shoaee, M;
Morris, J;
Brier, T;
Kara, E;
Sheerin, UM;
Charlesworth, G;
... Schapira, AH; + view all
(2014)
Analysis of Parkinson's disease brain-derived DNA for alpha-synuclein coding somatic mutations.
Mov Disord
, 29
(8)
060-1064.
10.1002/mds.25883.
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Tuschl, K;
Meyer, E;
Valdivia, LE;
Zhao, N;
Dadswell, C;
Abdul-Sada, A;
Hung, CY;
... Wilson, SW; + view all
(2016)
Mutations in SLC39A14 disrupt manganese homeostasis and cause childhood-onset parkinsonism-dystonia.
Nature Communications
, 7
, Article 11601. 10.1038/ncomms11601.
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Vavouraki, N;
Tomkins, JE;
Kara, E;
Houlden, H;
Hardy, J;
Tindall, MJ;
Lewis, PA;
(2021)
Integrating protein networks and machine learning for disease stratification in the Hereditary Spastic Paraplegias.
iScience
, Article 102484. 10.1016/j.isci.2021.102484.
(In press).
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Xiromerisiou, G;
Dardiotis, E;
Tsironi, EE;
Hadjigeorgiou, G;
Ralli, S;
Kara, E;
Petalas, A;
... Houlden, H; + view all
(2013)
THAP1 mutations in a Greek primary blepharospasm series.
Parkinsonism & Related Disorders
, 19
(3)
404 - 405.
10.1016/j.parkreldis.2012.08.015.
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Thesis
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Kara, E;
(2014)
The genetic basis and pathogenesis of Parkinson's disease and complex parkinsonisms.
Doctoral thesis , UCL (University College London).
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