Michael Farrell
Michael Farrell
Neznámá organizace
E-mailová adresa ověřena na:
Amyloid-β protein dimers isolated directly from Alzheimer's brains impair synaptic plasticity and memory
GM Shankar, S Li, TH Mehta, A Garcia-Munoz, NE Shepardson, I Smith, ...
Nature medicine 14 (8), 837-842, 2008
DNA methylation-based classification of central nervous system tumours
D Capper, DTW Jones, M Sill, V Hovestadt, D Schrimpf, D Sturm, ...
Nature 555 (7697), 469-474, 2018
Integrated molecular meta-analysis of 1,000 pediatric high-grade and diffuse intrinsic pontine glioma
A Mackay, A Burford, D Carvalho, E Izquierdo, J Fazal-Salom, KR Taylor, ...
Cancer cell 32 (4), 520-537. e5, 2017
Silencing microRNA-134 produces neuroprotective and prolonged seizure-suppressive effects
EM Jimenez-Mateos, T Engel, P Merino-Serrais, RC McKiernan, ...
Nature medicine 18 (7), 1087-1094, 2012
MCP-1, MCP-2 and MCP-3 expression in multiple sclerosis lesions: an immunohistochemical and in situ hybridization study
C McManus, JW Berman, FM Brett, H Staunton, M Farrell, CF Brosnan
Journal of neuroimmunology 86 (1), 20-29, 1998
Microdysgenesis in resected temporal neocortex: incidence and clinical significance in focal epilepsy
O Hardiman, T Burke, J Phillips, S Murphy, B O'moore, H Staunton, ...
Neurology 38 (7), 1041-1041, 1988
Progressive myoclonic epilepsies: a review of genetic and therapeutic aspects
A Shahwan, M Farrell, N Delanty
The Lancet Neurology 4 (4), 239-248, 2005
Alzheimer's disease brain-derived amyloid-β-mediated inhibition of LTP in vivo is prevented by immunotargeting cellular prion protein
AE Barry, I Klyubin, JM Mc Donald, AJ Mably, MA Farrell, M Scott, ...
Journal of Neuroscience 31 (20), 7259-7263, 2011
Infant high-grade gliomas comprise multiple subgroups characterized by novel targetable gene fusions and favorable outcomes
M Clarke, A Mackay, B Ismer, JC Pickles, RG Tatevossian, S Newman, ...
Cancer discovery 10 (7), 942-963, 2020
Neuropathologic findings in cortical resections (including hemispherectomies) performed for the treatment of intractable childhood epilepsy
MA Farrell, MJ DeRosa, JG Curran, D Lenard Secor, ME Cornford, ...
Acta neuropathologica 83, 246-259, 1992
Adenosine monophosphate-activated protein kinase disease mimicks hypertrophic cardiomyopathy and Wolff-Parkinson-White syndrome: natural history
RT Murphy, J Mogensen, K McGarry, A Bahl, A Evans, E Osman, P Syrris, ...
Journal of the American College of Cardiology 45 (6), 922-930, 2005
The ROAM/EORTC-1308 trial: radiation versus observation following surgical resection of atypical meningioma: study protocol for a randomised controlled trial
MD Jenkinson, M Javadpour, BJ Haylock, B Young, H Gillard, J Vinten, ...
Trials 16, 1-8, 2015
A prospective study of complications associated with cuffed, tunnelled haemodialysis catheters
MA Little, A O'Riordan, B Lucey, M Farrell, M Lee, PJ Conlon, JJ Walshe
Nephrology Dialysis Transplantation 16 (11), 2194-2200, 2001
Kufs disease, the major adult form of neuronal ceroid lipofuscinosis, caused by mutations in CLN6
T Arsov, KR Smith, J Damiano, S Franceschetti, L Canafoglia, ...
The American Journal of Human Genetics 88 (5), 566-573, 2011
Methods and apparatus for monitoring the cardiovascular condition of patients with sleep disordered breathing
M Farrell, M Hebblewhite, D Stewart, A Tisthammer, M Vance, ...
US Patent 7,878,198, 2011
Recessive mutations in RYR1 are a common cause of congenital fiber type disproportion
NF Clarke, LB Waddell, ST Cooper, M Perry, RLL Smith, AJ Kornberg, ...
Human mutation 31 (7), E1544-E1550, 2010
Mutations in the SPG7 gene cause chronic progressive external ophthalmoplegia through disordered mitochondrial DNA maintenance
G Pfeffer, GS Gorman, H Griffin, M Kurzawa-Akanbi, EL Blakely, I Wilson, ...
Brain 137 (5), 1323-1336, 2014
Parkin disease: a clinicopathologic entity?
KM Doherty, L Silveira-Moriyama, L Parkkinen, DG Healy, M Farrell, ...
JAMA neurology 70 (5), 571-579, 2013
Transient P2X7 receptor antagonism produces lasting reductions in spontaneous seizures and gliosis in experimental temporal lobe epilepsy
A Jimenez-Pacheco, M Diaz-Hernandez, M Arribas-Blázquez, ...
Journal of Neuroscience 36 (22), 5920-5932, 2016
Deficiency of respiratory chain complex I is a common cause of Leigh disease
AAM Morris, JV Leonard, GK Brown, SK Bidouki, LA Bindoff, DM Turnbull, ...
Annals of Neurology: Official Journal of the American Neurological …, 1996
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Články 1–20