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Results 31-40 of 42 (Search time: 0.003 seconds).
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PreviewIssue DateTitleAuthor(s)
2002Mutations in PHF6 are associated with Börjeson-Forssman-Lehmann syndromeLower, K.; Turner, G.; Kerr, B.; Mathews, K.; Shaw, M.; Gedeon, A.; Schelley, S.; Hoyme, H.; White, S.; Delatycki, M.; Lampe, A.; Clayton-Smith, J.; Stewart, H.; van Ravenswaay, C.; de Vries, B.; Cox, B.; Grompe, M.; Ross, S.; Thomas, P.; Mulley, J.; et al.
2009Rosuvastatin and Cardiovascular Events in Patients Undergoing HemodialysisFellstrom, B.; Jardine, A.; Schmeider, R.; Holdaas, H.; Bannister, K.; Beutler, J.; Chae, D.; Chevaile, A.; Cobbe, S.; Gronhagen-Riska, C.; De Lima, J.; Lins, R.; Mayer, G.; McMahon, A.; Parving, H.; Samuelsson, O.; Sonkodi, S.; Suleymanlar, G.; Tsakiris, D.; Tesar, V.; et al.
2003Imatinib compared with interferon and low-dose cytarabine for newly diagnosed chronic-phase chronic myeloid leukemiaO'Brien, S.; Guilhot, F.; Larson, R.; Gathmann, I.; Baccarani, M.; Cervantes, F.; Cornelissen, J.; Fischer, T.; Hochhaus, A.; Hughes, T.; Lechner, K.; Nielsen, J.; Rousselot, P.; Reiffers, J.; Saglio, G.; Shepherd, J.; Simonsson, B.; Gratwohl, A.; Goldman, J.; Kantarjian, H.; et al.
2003Mutations in the polyglutamine binding protein 1 gene cause X-linked mental retardationKalscheuer, V.; Freude, K.; Musante, L.; Jensen, L.; Yntema, H.; Gecz, J.; Sefiani, A.; Hoffmann, K.; Moser, B.; Haas, S.; Gurok, U.; Haesler, S.; Aranda, B.; Nshedjan, A.; Tzschach, A.; Hartmann, N.; Roloff, T.; Shoichet, S.; Hagens, O.; Tao, J.; et al.
2008Effects of alteplase beyond 3 h after stroke in the Echoplanar Imaging Thrombolytic Evaluation Trial (EPITHET): a placebo-controlled randomised trialDavis, S.; Donnan, G.; Parsons, M.; Levi, C.; Butcher, K.; Peeters, A.; Barber, P.; Bladin, C.; De Silva, D.; Byrnes, G.; Chalk, J.; Fink, J.; Kimber, T.; Schultz, D.; Hand, P.; Frayne, J.; Hankey, G.; Muir, K.; Gerraty, R.; Tress, B.; et al.
2003Fluoropolymer coated Dacron or polytetrafluoroethylene for femoropopliteal bypass grafting: a multicentre trialRobinson, B.; Fletcher, J.; Richardson, A.; Tomlinson, P.; Bell, R.; Fisher, C.; Condous, M.; Ventura, R.; Scott, A.; Stary, D.; Allen, R.; Lippey, E.; Appleberg, M.; Chao, A.; Fitridge, R.; Frydman, G.; Hazelton, S.; King, B.; Middleton, P.; Pai, P.; et al.
2009Genome sequence, comparative analysis, and population genetics of the domestic horseWade, C.; Giulotto, E.; Sigurdsson, S.; Zoli, M.; Gnerre, S.; Imsland, F.; Lear, T.; Adelson, D.; Bailey, E.; Bellone, R.; Blocker, H.; Distl, O.; Edgar, R.; Garber, M.; Leeb, T.; Mauceli, E.; Macleod, J.; PENEDO, M.; Raison, J.; Sharpe, T.; et al.
2006The effect of modifiable risk factors on pancreatic cancer mortality in populations of the Asia-Pacific regionAnsary-Moghaddam, A.; Huxley, R.; Barzi, F.; Lawes, C.; Ohkubo, T.; Fang, X.; Jee, S.; Woodward, M.; Okayama, A.; Ueshima, H.; Maegawa, H.; Aoki, N.; Nakamura, M.; Kubo, N.; Yamada, T.; Wu, Z.; Yao, C.; Andrews, G.; Welborn, T.; Tang, Z.; et al.
2008The association of C-reactive protein and CRP genotype with coronary heart disease: findings from five studies with 4610 cases amongst 18637 participantsLawlor, D.; Harbord, R.; Timpson, N.; Lowe, G.; Rumley, A.; Gaunt, T.; Baker, I.; Yarnell, J.; Kivimaki, M.; Kumari, M.; Norman, P.; Jamrozik, K.; Hankey, G.; Almeida, O.; Flicker, L.; Warrington, N.; Marmot, M.; Ben-Shlomo, Y.; Palmer, L.; Day, I.; et al.; Keavney, B.
2006Analysis of cancer risk and BRCA1 and BRCA2 mutation prevalence in the kConFab familial breast cancer resourceMann, G.; Thorne, H.; Balleine, R.; Butow, P.; Clarke, C.; Edkins, E.; Evans, G.; Fereday, S.; Haan, E.; Gattas, M.; Giles, G.; Goldblatt, J.; Hopper, J.; Kirk, J.; Leary, J.; Lindeman, G.; Niedermayr, E.; Phillips, K.; Picken, S.; Pupo, G.; et al.