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Kevin Talbot
Kevin Talbot
Professor of Neurology, Oxford University
Bestätigte E-Mail-Adresse bei ndcn.ox.ac.uk
Titel
Zitiert von
Zitiert von
Jahr
Frequency of the C9orf72 hexanucleotide repeat expansion in patients with amyotrophic lateral sclerosis and frontotemporal dementia: a cross-sectional study
E Majounie, AE Renton, K Mok, EGP Dopper, A Waite, S Rollinson, ...
The Lancet Neurology 11 (4), 323-330, 2012
12012012
Mutant small heat-shock protein 27 causes axonal Charcot-Marie-Tooth disease and distal hereditary motor neuropathy
OV Evgrafov, I Mersiyanova, J Irobi, L Van Den Bosch, I Dierick, CL Leung, ...
Nature genetics 36 (6), 602-606, 2004
7172004
Controversies and priorities in amyotrophic lateral sclerosis
MR Turner, O Hardiman, M Benatar, BR Brooks, A Chio, M De Carvalho, ...
The Lancet Neurology 12 (3), 310-322, 2013
5922013
Transgenics, toxicity and therapeutics in rodent models of mutant SOD1-mediated familial ALS
BJ Turner, K Talbot
Progress in neurobiology 85 (1), 94-134, 2008
5922008
Biomarkers in amyotrophic lateral sclerosis
MR Turner, MC Kiernan, PN Leigh, K Talbot
The Lancet Neurology 8 (1), 94-109, 2009
4952009
Hot-spot residue in small heat-shock protein 22 causes distal motor neuropathy
J Irobi, KV Impe, P Seeman, A Jordanova, I Dierick, N Verpoorten, ...
Nature genetics 36 (6), 597-601, 2004
4832004
Genome-wide analyses identify KIF5A as a novel ALS gene
A Nicolas, KP Kenna, AE Renton, N Ticozzi, F Faghri, R Chia, ...
Neuron 97 (6), 1268-1283. e6, 2018
4812018
Neurofilament light chain: a prognostic biomarker in amyotrophic lateral sclerosis
CH Lu, C Macdonald-Wallis, E Gray, N Pearce, A Petzold, N Norgren, ...
Neurology 84 (22), 2247-2257, 2015
4382015
Selective vulnerability of motor neurons and dissociation of pre-and post-synaptic pathology at the neuromuscular junction in mouse models of spinal muscular atrophy
LM Murray, LH Comley, D Thomson, N Parkinson, K Talbot, ...
Human molecular genetics 17 (7), 949-962, 2008
4092008
Exome-wide rare variant analysis identifies TUBA4A mutations associated with familial ALS
BN Smith, N Ticozzi, C Fallini, AS Gkazi, S Topp, KP Kenna, EL Scotter, ...
Neuron 84 (2), 324-331, 2014
3782014
Long-term effectiveness of dopamine agonists and monoamine oxidase B inhibitors compared with levodopa as initial treatment for Parkinson's disease (PD MED): a large, open …
PD Med Collaborative Group
The Lancet 384 (9949), 1196-1205, 2014
3642014
Unbiased screen for interactors of leucine-rich repeat kinase 2 supports a common pathway for sporadic and familial Parkinson disease
A Beilina, IN Rudenko, A Kaganovich, L Civiero, H Chau, SK Kalia, ...
Proceedings of the National Academy of Sciences 111 (7), 2626-2631, 2014
3622014
Loss of VPS13C function in autosomal-recessive parkinsonism causes mitochondrial dysfunction and increases PINK1/Parkin-dependent mitophagy
S Lesage, V Drouet, E Majounie, V Deramecourt, M Jacoupy, A Nicolas, ...
The American Journal of Human Genetics 98 (3), 500-513, 2016
3442016
Prognosis for patients with amyotrophic lateral sclerosis: development and validation of a personalised prediction model
HJ Westeneng, TPA Debray, AE Visser, RPA van Eijk, JPK Rooney, ...
The Lancet Neurology 17 (5), 423-433, 2018
3432018
Excessive burden of lysosomal storage disorder gene variants in Parkinson’s disease
LA Robak, IE Jansen, J Van Rooij, AG Uitterlinden, R Kraaij, J Jankovic, ...
Brain 140 (12), 3191-3203, 2017
3262017
Corpus callosum involvement is a consistent feature of amyotrophic lateral sclerosis
N Filippini, G Douaud, CE Mackay, S Knight, K Talbot, MR Turner
Neurology 75 (18), 1645-1652, 2010
3072010
ER Stress and Autophagic Perturbations Lead to Elevated Extracellular α-Synuclein in GBA-N370S Parkinson's iPSC-Derived Dopamine Neurons
HJR Fernandes, EM Hartfield, HC Christian, E Emmanoulidou, Y Zheng, ...
Stem cell reports 6 (3), 342-356, 2016
3012016
Extracellular vesicles in neurodegenerative disease—pathogenesis to biomarkers
AG Thompson, E Gray, SM Heman-Ackah, I Mäger, K Talbot, ...
Nature Reviews Neurology 12 (6), 346-357, 2016
2972016
Deletions in the survival motor neuron gene on 5q13 in autosomal recessive spinal muscular atrophy
NR Rodrigues, N Owen, K Talbot, J Ignatius, V Dubowitz, KE Davies
Human Molecular Genetics 4 (4), 631-634, 1995
2901995
The influence of age and gender on motor and non-motor features of early Parkinson's disease: initial findings from the Oxford Parkinson Disease Center (OPDC) discovery cohort
K Szewczyk-Krolikowski, P Tomlinson, K Nithi, R Wade-Martins, K Talbot, ...
Parkinsonism & related disorders 20 (1), 99-105, 2014
2822014
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