Andrew T King
Andrew T King
Professor of Neurosurgery, Salford Royal Hospital, MAHSC, University of Manchester
Verified email at manchester.ac.uk
Title
Cited by
Cited by
Year
Investigation of variant Creutzfeldt-Jakob disease and other human prion diseases with tonsil biopsy samples
AF Hill, RJ Butterworth, S Joiner, G Jackson, MN Rossor, DJ Thomas, ...
The Lancet 353 (9148), 183-189, 1999
8131999
p62 positive, TDP-43 negative, neuronal cytoplasmic and intranuclear inclusions in the cerebellum and hippocampus define the pathology of C9orf72-linked FTLD …
S Al-Sarraj, A King, C Troakes, B Smith, S Maekawa, I Bodi, B Rogelj, ...
Acta neuropathologica 122 (6), 691-702, 2011
4372011
The genetics and neuropathology of amyotrophic lateral sclerosis
A Al-Chalabi, A Jones, C Troakes, A King, S Al-Sarraj, LH Van Den Berg
Acta neuropathologica 124 (3), 339-352, 2012
3912012
Trends in head injury outcome from 1989 to 2003 and the effect of neurosurgical care: an observational study
HC Patel, O Bouamra, M Woodford, AT King, DW Yates, FE Lecky
The Lancet 366 (9496), 1538-1544, 2005
3842005
Staging of neurofibrillary pathology in Alzheimer's disease: a study of the BrainNet Europe Consortium
I Alafuzoff, T Arzberger, S Al‐Sarraj, I Bodi, N Bogdanovic, H Braak, ...
Brain pathology 18 (4), 484-496, 2008
3562008
Incidence of vestibular schwannoma and neurofibromatosis 2 in the North West of England over a 10-year period: higher incidence than previously thought
DGR Evans, A Moran, A King, S Saeed, N Gurusinghe, R Ramsden
Otology & Neurotology 26 (1), 93-97, 2005
3362005
Clinical and neuroanatomical signatures of tissue pathology in frontotemporal lobar degeneration
JD Rohrer, T Lashley, JM Schott, JE Warren, S Mead, AM Isaacs, J Beck, ...
Brain 134 (9), 2565-2581, 2011
2872011
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
2642014
Staging/typing of Lewy body related α-synuclein pathology: a study of the BrainNet Europe Consortium
I Alafuzoff, PG Ince, T Arzberger, S Al-Sarraj, J Bell, I Bodi, N Bogdanovic, ...
Acta neuropathologica 117 (6), 635-652, 2009
2252009
Management of the patient and family with neurofibromatosis 2: a consensus conference statement
DGR Evans, ME Baser, B O'reilly, J Rowe, M Gleeson, S Saeed, A King, ...
British journal of neurosurgery 19 (1), 5-12, 2005
2242005
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
2182018
A distinct clinical, neuropsychological and radiological phenotype is associated with progranulin gene mutations in a large UK series
J Beck, JD Rohrer, T Campbell, A Isaacs, KE Morrison, EF Goodall, ...
Brain 131 (3), 706-720, 2008
2172008
NEK1 variants confer susceptibility to amyotrophic lateral sclerosis
KP Kenna, PTC Van Doormaal, AM Dekker, N Ticozzi, BJ Kenna, ...
Nature genetics 48 (9), 1037-1042, 2016
1582016
Spinal meningiomas: a 20-year review
AT King, MM Sharr, RW Gullan, JR Bartlett
British journal of neurosurgery 12 (6), 521-526, 1998
1441998
Assessment of β-amyloid deposits in human brain: a study of the BrainNet Europe Consortium
I Alafuzoff, DR Thal, T Arzberger, N Bogdanovic, S Al-Sarraj, I Bodi, ...
Acta neuropathologica 117 (3), 309-320, 2009
1402009
Mutations in RYR1 are a common cause of exertional myalgia and rhabdomyolysis
N Dlamini, NC Voermans, S Lillis, K Stewart, EJ Kamsteeg, G Drost, ...
Neuromuscular Disorders 23 (7), 540-548, 2013
1362013
Aluminium in brain tissue in familial Alzheimer’s disease
A Mirza, A King, C Troakes, C Exley
Journal of Trace Elements in Medicine and Biology 40, 30-36, 2017
1332017
TDP‐43 is consistently co‐localized with ubiquitinated inclusions in sporadic and Guam amyotrophic lateral sclerosis but not in familial amyotrophic lateral sclerosis with and …
S Maekawa, PN Leigh, A King, E Jones, JC Steele, I Bodi, CE Shaw, ...
Neuropathology 29 (6), 672-683, 2009
1312009
Aluminium in brain tissue in autism
M Mold, D Umar, A King, C Exley
Journal of Trace Elements in Medicine and Biology 46, 76-82, 2018
1242018
An MND/ALS phenotype associated with C9orf72 repeat expansion: Abundant p62‐positive, TDP‐43‐negative inclusions in cerebral cortex, hippocampus and …
C Troakes, S Maekawa, L Wijesekera, B Rogelj, L Siklós, C Bell, B Smith, ...
Neuropathology 32 (5), 505-514, 2012
1172012
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