Browse by UCL people
Group by: Type | Date
Number of items: 6.
Article
Chelban, V;
Tucci, A;
Lynch, DS;
Polke, JM;
Santos, L;
Jonvik, H;
Groppa, S;
... Houlden, H; + view all
(2017)
Truncating mutations in SPAST patients are associated with a high rate of psychiatric comorbidities in hereditary spastic paraplegia.
Journal of Neurology Neurosurgery and Psychiatry
, 88
(8)
10.1136/jnnp-2017-315796.
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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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Lynch, DS;
Koutsis, G;
Tucci, A;
Panas, M;
Baklou, M;
Breza, M;
Karadima, G;
(2016)
Hereditary spastic paraplegia in Greece: characterisation of a previously unexplored population using next-generation sequencing.
European Journal of Human Genetics
, 24
(6)
pp. 857-863.
10.1038/ejhg.2015.200.
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Schottlaender, LV;
Polke, JM;
Ling, H;
MacDoanld, ND;
Tucci, A;
Nanji, T;
Pittman, A;
... Houlden, H; + view all
(2015)
The analysis of C9orf72 repeat expansions in a large series of clinically and pathologically diagnosed cases with atypical parkinsonism.
Neurobiol Aging
, 36
(2)
1221.e1 - 1221.e6.
10.1016/j.neurobiolaging.2014.08.024.
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Tucci, A;
Charlesworth, G;
Sheerin, UM;
Plagnol, V;
Wood, NW;
Hardy, J;
(2012)
Study of the genetic variability in a Parkinson's Disease gene: EIF4G1.
Neurosci Lett
, 518
(1)
19 - 22.
10.1016/j.neulet.2012.04.033.
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Thesis
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Tucci, A;
(2013)
The use of next generation sequencing technologies to dissect the aetiologies of neurodegenerative diseases.
Doctoral thesis (PhD), UCL (University College London).
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