Heterogeneity in Longitudinal Healthcare Utilisation by Older Adults: A Latent Transition Analysis of the Irish Longitudinal Study on Ageing

por Doherty, Ann S, Miller, Ruth, Mallett, John, Adamson, Gary
Publicado 2021

Suppression of cathepsin K biomarker in synovial fluid as a free-drug–driven process

por Ma, Bennett, Wesolowski, Gregg, Luo, Bin, Lifsted, Traci, Wessner, Keith, Adamson, Gary, Glantschnig, Helmut, Lubbers, Laura S
Publicado 2019

Axial growth and refractive change in white European children and young adults: predictive factors for myopia

por McCullough, Sara, Adamson, Gary, Breslin, Karen M. M., McClelland, Julie F., Doyle, Lesley, Saunders, Kathryn J.
Publicado 2020

Variants of PLCXD3 are not associated with variant or sporadic Creutzfeldt-Jakob disease in a large international study

por Balendra, Rubika, Uphill, James, Collinson, Claire, Druyeh, Ronald, Adamson, Gary, Hummerich, Holger, Zerr, Inga, Gambetti, Pierluigi, Collinge, John, Mead, Simon
Publicado 2016

A novel prion protein variant in a patient with semantic dementia

por Kenny, Joanna, Woollacott, Ione, Koriath, Carolin, Hosszu, Laszlo, Adamson, Gary, Rudge, Peter, Rossor, Martin N, Collinge, John, Rohrer, Jonathan D, Mead, Simon
Publicado 2017

Genetic risk factors for variant Creutzfeldt–Jakob disease: a genome-wide association study

por Mead, Simon, Poulter, Mark, Uphill, James, Beck, John, Whitfield, Jerome, Webb, Thomas EF, Campbell, Tracy, Adamson, Gary, Deriziotis, Pelagia, Tabrizi, Sarah J, Hummerich, Holger, Verzilli, Claudio, Alpers, Michael P, Whittaker, John C, Collinge, John
Publicado 2009

Establishing a clinical phenotype for cachexia in end stage kidney disease – study protocol

por Reid, Joanne, Noble, Helen R., Adamson, Gary, Davenport, Andrew, Farrington, Ken, Fouque, Denis, Kalantar-Zadeh, Kamyar, Mallett, John, McKeaveney, C., Porter, S., Seres, David S., Shields, Joanne, Slee, Adrian, Witham, Miles D., Maxwell, Alexander P.
Publicado 2018

Screening a UK amyotrophic lateral sclerosis cohort provides evidence of multiple origins of the C9orf72 expansion()

por Fratta, Pietro, Polke, James M., Newcombe, Jia, Mizielinska, Sarah, Lashley, Tammaryn, Poulter, Mark, Beck, Jon, Preza, Elisavet, Devoy, Anny, Sidle, Katie, Howard, Robin, Malaspina, Andrea, Orrell, Richard W., Clarke, Jan, Lu, Ching-Hua, Mok, Kin, Collins, Toby, Shoaii, Maryam, Nanji, Tina, Wray, Selina, Adamson, Gary, Pittman, Alan, Renton, Alan E., Traynor, Bryan J., Sweeney, Mary G., Revesz, Tamas, Houlden, Henry, Mead, Simon, Isaacs, Adrian M., Fisher, Elizabeth M.C.
Publicado 2015

FUS pathology defines the majority of tau- and TDP-43-negative frontotemporal lobar degeneration

por Urwin, Hazel, Josephs, Keith A., Rohrer, Jonathan D., Mackenzie, Ian R., Neumann, Manuela, Authier, Astrid, Seelaar, Harro, Van Swieten, John C., Brown, Jeremy M., Johannsen, Peter, Nielsen, Jorgen E., Holm, Ida E., Dickson, Dennis W., Rademakers, Rosa, Graff-Radford, Neill R., Parisi, Joseph E., Petersen, Ronald C., Hatanpaa, Kimmo J., White III, Charles L., Weiner, Myron F., Geser, Felix, Van Deerlin, Vivianna M., Trojanowski, John Q., Miller, Bruce L., Seeley, William W., van der Zee, Julie, Kumar-Singh, Samir, Engelborghs, Sebastiaan, De Deyn, Peter P., Van Broeckhoven, Christine, Bigio, Eileen H., Deng, Han-Xiang, Halliday, Glenda M., Kril, Jillian J., Munoz, David G., Mann, David M., Pickering-Brown, Stuart M., Doodeman, Valerie, Adamson, Gary, Ghazi-Noori, Shabnam, Fisher, Elizabeth M. C., Holton, Janice L., Revesz, Tamas, Rossor, Martin N., Collinge, John, Mead, Simon, Isaacs, Adrian M.
Publicado 2010