Zobrazeno 1 - 10
of 292
pro vyhledávání: '"Carroll, SL"'
Publikováno v:
Patient Preference and Adherence, Vol Volume 12, Pp 1947-1954 (2018)
Sandra L Carroll,1–3 Gayathri Embuldeniya,3 Jasprit Pannag,1 Krystina B Lewis,4 Jeff S Healey,2,3,5 Michael McGillion,1,2 Lehana Thabane,2,6,7 Dawn Stacey4,8 1School of Nursing, McMaster University, Hamilton, ON, Canada; 2Population Health Research
Externí odkaz:
https://doaj.org/article/d080b03459904eab97ab7767e023e159
Publikováno v:
Patient Preference and Adherence, Vol Volume 11, Pp 1573-1583 (2017)
Sandra L Carroll,1 Gayathri Embuldeniya,1 Julia Abelson,2 Michael McGillion,1 Alexandre Berkesse,3 Jeff S Healey4 1Faculty of Health Sciences, School of Nursing, McMaster University, Hamilton, ON, 2Faculty of Health Sciences, Health Research Methods,
Externí odkaz:
https://doaj.org/article/f459c501009b44b68b5619dc4f7e571e
Publikováno v:
JMIR mHealth and uHealth
Autor:
Hamlett, ED, Goetzl, EJ, Ledreux, A, Vasilevko, V, Boger, HA, LaRosa, A, Clark, D, Carroll, SL, Carmona-Iragui, M, Fortea, J, Mufson, EJ, Sabbagh, M, Mohammed, AH, Hartley, D, Doran, E, Lott, IT, Granholm, AC
Publikováno v:
Alzheimers & Dementia
r-IIB SANT PAU. Repositorio Institucional de Producción Científica del Instituto de Investigación Biomédica Sant Pau
instname
r-IIB SANT PAU. Repositorio Institucional de Producción Científica del Instituto de Investigación Biomédica Sant Pau
instname
Introduction: Individuals with Down syndrome (DS) exhibit Alzheimer's disease (AD) neuropathology and dementia early in life. Blood biomarkers of AD neuropathology would be valuable, as non-AD intellectual disabilities of DS and AD dementia overlap c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=RECOLECTA___::59076527b07a3ea8d0c254acb59279b3
https://iibsantpau.fundanetsuite.com/Publicaciones/ProdCientif/PublicacionFrw.aspx?id=6474
https://iibsantpau.fundanetsuite.com/Publicaciones/ProdCientif/PublicacionFrw.aspx?id=6474
Autor:
Whitcomb, DC, LaRusch, J, Krasinskas, AM, Klei, L, Smith, JP, Brand, RE, Neoptolemos, JP, Lerch, MM, Tector, M, Sandhu, BS, Guda, NM, Orlichenko, L, Alkaade, S, Amann, ST, Anderson, MA, Baillie, J, Banks, PA, Conwell, D, Coté, GA, Cotton, PB, DiSario, J, Farrer, LA, Forsmark, CE, Johnstone, M, Gardner, TB, Gelrud, A, Greenhalf, W, Haines, JL, Hartman, DJ, Hawes, RA, Lawrence, C, Lewis, M, Mayerle, J, Mayeux, R, Melhem, NM, Money, ME, Muniraj, T, Papachristou, GI, Pericak-Vance, MA, Romagnuolo, J, Schellenberg, GD, Sherman, S, Simon, P, Singh, VP, Slivka, A, Stolz, D, Sutton, R, Weiss, FU, Wilcox, CM, Zarnescu, NO, Wisniewski, SR, O'Connell, MR, Kienholz, ML, Roeder, K, Barmada, MM, Yadav, D, Devlin, B, Albert, MS, Albin, RL, Apostolova, LG, Arnold, SE, Baldwin, CT, Barber, R, Barnes, LL, Beach, TG, Beecham, GW, Beekly, D, Bennett, DA, Bigio, EH, Bird, TD, Blacker, D, Boxer, A, Burke, JR, Buxbaum, JD, Cairns, NJ, Cantwell, LB, Cao, C, Carney, RM, Carroll, SL, Chui, HC, Clark, DG, Cribbs, DH, Crocco, EA, Cruchaga, C
Publikováno v:
Whitcomb, DC; LaRusch, J; Krasinskas, AM; Klei, L; Smith, JP; Brand, RE; et al.(2012). Common genetic variants in the CLDN2 and PRSS1-PRSS2 loci alter risk for alcohol-related and sporadic pancreatitis. Nature Genetics, 44(12), 1349-1354. doi: 10.1038/ng.2466. UC Davis: Retrieved from: http://www.escholarship.org/uc/item/1br4p91m
Pancreatitis is a complex, progressively destructive inflammatory disorder. Alcohol was long thought to be the primary causative agent, but genetic contributions have been of interest since the discovery that rare PRSS1, CFTR and SPINK1 variants were
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od_______325::418cbf8873cdf89841e8cf7bdc42392e
http://www.escholarship.org/uc/item/1br4p91m
http://www.escholarship.org/uc/item/1br4p91m
Autor:
Naj, AC, Jun, G, Beecham, GW, Wang, LS, Vardarajan, BN, Buros, J, Gallins, PJ, Buxbaum, JD, Jarvik, GP, Crane, PK, Larson, EB, Bird, TD, Boeve, BF, Graff-Radford, NR, De Jager, PL, Evans, D, Schneider, JA, Carrasquillo, MM, Ertekin-Taner, N, Younkin, SG, Cruchaga, C, Kauwe, JSK, Nowotny, P, Kramer, P, Hardy, J, Huentelman, MJ, Myers, AJ, Barmada, MM, Demirci, FY, Baldwin, CT, Green, RC, Rogaeva, E, George-Hyslop, PS, Arnold, SE, Barber, R, Beach, T, Bigio, EH, Bowen, JD, Boxer, A, Burke, JR, Cairns, NJ, Carlson, CS, Carney, RM, Carroll, SL, Chui, HC, Clark, DG, Corneveaux, J, Cotman, CW, Cummings, JL, Decarli, C, Dekosky, ST, Diaz-Arrastia, R, Dick, M, Dickson, DW, Ellis, WG, Faber, KM, Fallon, KB, Farlow, MR, Ferris, S, Frosch, MP, Galasko, DR, Ganguli, M, Gearing, M, Geschwind, DH, Ghetti, B, Gilbert, JR, Gilman, S, Giordani, B, Glass, JD, Growdon, JH, Hamilton, RL, Harrell, LE, Head, E, Honig, LS, Hulette, CM, Hyman, BT, Jicha, GA, Jin, LW, Johnson, N, Karlawish, J, Karydas, A, Kaye, JA, Kim, R
Publikováno v:
Naj, AC; Jun, G; Beecham, GW; Wang, LS; Vardarajan, BN; Buros, J; et al.(2011). Common variants at MS4A4/MS4A6E, CD2AP, CD33 and EPHA1 are associated with late-onset Alzheimer's disease. Nature Genetics, 43(5), 436-443. doi: 10.1038/ng.801. UC Irvine: Retrieved from: http://www.escholarship.org/uc/item/6xc596k3
The Alzheimer Disease Genetics Consortium (ADGC) performed a genome-wide association study of late-onset Alzheimer disease using a three-stage design consisting of a discovery stage (stage 1) and two replication stages (stages 2 and 3). Both joint an
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od_______325::9f53ff000ffc5d3502416acdaff6517b
http://www.escholarship.org/uc/item/6xc596k3
http://www.escholarship.org/uc/item/6xc596k3
Autor:
McGillion, Michael, Cook ,Alison, Victor,J. Charles, Arthur ,Heather, Teoh ,Kevin, Carroll,SL, Weston ,Julie
Publikováno v:
Vascular Health and Risk Management.
Michael McGillion1, Allison Cook2, J Charles Victor3, Sandra Carroll2, Julie Weston1, Kevin Teoh4, Heather M Arthur21University of Toronto, 3Dalla Lana School of Public Health, Toronto, ON, Canada; 2McMaster University, Faculty of Health Sciences, Ha
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