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Stephen Murphy, Soon Tjin Lim, Justin Kinsella, Sean Tierney, Bridget Egan, T Martin Feeley, Sinead Murphy, Richard Walsh, Ronan Collins, Tara Coughlan, Desmond O'Neill, Sean O'Neill, Joseph Harbison, Prakash Madhavan, Mary Paula Colgan, Dermot Cox, Niamh Moran, George Hamilton, Dominick McCabe, On-treatment platelet reactivity' under both high and low shear stress conditions and relationship with cerebral micro-embolic signals in asymptomatic and symptomatic carotid stenosis: Results from the HaEmostasis In carotid STenosis(HEIST) study, Neurology, American Academy of Neurology, Philadelphia, May 4 - May 11 2019, 92, (Supp 15), 2019,
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. Murphy SJX, Lim ST, Kinsella JA, Tierney S, Egan B, Feeley TM, Murphy SM, Walsh RA, Collins DR, Coughlan T, O'Neill D, Harbison JA, Madhavan P, O'Neill SM, Colgan MP, Cox D, Moran N, Hamilton G, McCabe DJH, Increased leucocyte-platelet complex formation in recently symptomatic versus asymptomatic carotid stenosis patients and in micro-emboli negative subgroups. , Thrombosis and Haemostasis , 2019,
Notes: [doi: 10.1055/s-0039-1678666],
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DA Olszewska, EM Fallon, GM Pastores, K Murphy, A Blanco, T Lynch, SM Murphy, Autosomal dominant gene negative frontotemporal dementia-think of SCA17, Cerebellum, 2019,
Notes: [doi: 10.1007/s12311-018-0998-2],
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Renaud, M., Moreira, M.-C., Monga, B.B., Rodriguez, D., Debs, R., Charles, P., Chaouch, M., Ferrat, F., Laurencin, C., Vercueil, L., Mallaret, M., M"Zahem, A., Pacha, L.A., Tazir, M., Tilikete, C., Ollagnon, E., Ochsner, F., Kuntzer, T., Jung, H.H., Beis, J.-M., Netter, J.-C., Djamshidian, A., Bower, M., Bottani, A., Walsh, R., Murphy, S., Reiley, T., Bieth, É., Roelens, F., Poll-The, B.T., Lourenço, C.M., Jardim, L.B., Straussberg, R., Landrieu, P., Roze, E., Thobois, S., Pouget, J., Guissart, C., Goizet, C., Dürr, A., Tranchant, C., Koenig, M., Anheim, M., Clinical, biomarker, and molecular delineations and genotype-Phenotype correlations of ataxia with oculomotor apraxia type 1, JAMA Neurology, 75, (4), 2018, p495-502 ,
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Bogdanova-Mihaylova, P., Murphy, R.P.J., Alexander, M.D., McHugh, J.C., Foley, A.R., Brett, F., Murphy, S.M., Congenital myasthenic syndrome due to DPAGT1 mutations mimicking congenital myopathy in an Irish family, European Journal of Neurology, 25, (2), 2018, pe22-e23 ,
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D'Alton M, Coughlan T, Cogan N, Greene S, McCabe DJH, McCarthy A, Murphy S, Walsh R, O'Neill D, Kennelly S, Ryan D, Collins R, Patterns of Mortality in Modern Stroke Care, Ir Med J, 111, (5), 2018, pP750 ,
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. Murphy SJX, Lim ST, Kinsella JA, Murphy D, Enright HM, McCabe DJH for the HEIST study group, Platelet count and profile of reticulated platelets and red cell reticulocytes in patients with recently symptomatic versus asymptomatic carotid stenosis: Results from the HaEmostasis In carotid STenosis (HEIST) study, Journal of Neurology , 265, 2018, p1037-,
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Bogdanova-Mihaylova, P., Burke, D., O"Dwyer, J.P., Bradley, D., Williams, J.A., Cronin, S.J., Smyth, S., Murphy, R.P., Murphy, S.M., Wall, C., McCabe, D.J.H., Aciclovir-induced acute kidney injury in patients with `suspected viral encephalitis" encountered on a liaison neurology service, Irish Journal of Medical Science, 2018, p1-4 ,
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J Panicker, M Lad, M Parkinson, M Rai, M Pandolfo, P Mihaylova-Bogdanova, RA Walsh, S Murphy, A Emmanuel, P Giunti, 'Lower urinary tract, bowel and sexual dysfunction in Friedreich’'s ataxia' , Journal of the Neurological Sciences, World Congress of Neurology, Kyoto, Japan, 2017, 2017,
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Rossor, A.M., Morrow, J.M., Polke, J.M., Murphy, S.M., Houlden, H., Laura, M., Manji, H., Blake, J., Reilly, M.M., Pilot phenotype and natural history study of hereditary neuropathies caused by mutations in the HSPB1 gene, Neuromuscular Disorders, 27, (1), 2017, p50-56 ,
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