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Results 21-30 of 680 (Search time: 0.001 seconds).
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First PublishedTitleAuthor(s)Type
Nov-2006The prevalence of co-morbid depression in adults with Type 2 diabetes: a systematic review and meta-analysis.Ali, S; Stone, MA; Peters, JL; Davies, MJ; Khunti, KJournal Article
Sep-2011Phase I randomized, double-blind pilot study of micronized resveratrol (SRT501) in patients with hepatic metastases--safety, pharmacokinetics, and pharmacodynamics.Howells, LM; Berry, DP; Elliott, PJ; Jacobson, EW; Hoffmann, E; Hegarty, B; Brown, K; Steward, WP; Gescher, AJJournal Article
Nov-2011Association of cardiac and non-cardiac chronic disease comorbidity on glycaemic control in a multi-ethnic population with type 1 and type 2 diabetes.Mehta, RL; Davies, MJ; Ali, S; Taub, NA; Stone, MA; Baker, R; McNally, PG; Lawrence, IG; Khunti, KJournal Article
Oct-2010Generic, symptom based, exercise rehabilitation; integrating patients with COPD and heart failure.Evans, RA; Singh, SJ; Collier, R; Loke, I; Steiner, MC; Morgan, MDJournal Article
Apr-2012Psychophysical correlates of global motion processing in the aging visual system: a critical review.Hutchinson, CV; Arena, A; Allen, HA; Ledgeway, TJournal Article
Apr-2010Cell loss in the motor and cingulate cortex correlates with symptomatology in Huntington's disease.Thu, DC; Oorschot, DE; Tippett, LJ; Nana, AL; Hogg, VM; Synek, BJ; Luthi-Carter, R; Waldvogel, HJ; Faull, RLJournal Article
Dec-2004Neostriatal and cortical quinolinate levels are increased in early grade Huntington's disease.Guidetti, P; Luthi-Carter, RE; Augood, SJ; Schwarcz, RJournal Article
15-Mar-2006Regional and cellular gene expression changes in human Huntington's disease brain.Hodges, A; Strand, AD; Aragaki, AK; Kuhn, A; Sengstag, T; Hughes, G; Elliston, LA; Hartog, C; Goldstein, DR; Thu, D; Hollingsworth, ZR; Collin, F; Synek, B; Holmans, PA; Young, AB; Wexler, NS; Delorenzi, M; Kooperberg, C; Augood, SJ; Faull, RL; Olson, JM; Jones, L; Luthi-Carter, RJournal Article
2012A novel missense mutation in both OPN1LW and OPN1MW cone opsin genes causes X-linked cone dystrophy (XLCOD5).Gardner, JC; Webb, TR; Kanuga, N; Robson, AG; Holder, GE; Stockman, A; Ripamonti, C; Ebenezer, ND; Ogun, O; Devery, S; Wright, GA; Maher, ER; Cheetham, ME; Moore, AT; Michaelides, M; Hardcastle, AJJournal Article
Jun-2010Hepatic metabolism and transporter gene variants enhance response to rosuvastatin in patients with acute myocardial infarction: the GEOSTAT-1 Study.Bailey, KM; Romaine, SP; Jackson, BM; Farrin, AJ; Efthymiou, M; Barth, JH; Copeland, J; McCormack, T; Whitehead, A; Flather, MD; Samani, NJ; Nixon, J; Hall, AS; Balmforth, AJ; SPACE ROCKET Trial GroupJournal Article