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Results 11-20 of 26 (Search time: 0.003 seconds).
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PreviewIssue DateTitleAuthor(s)
2018A genome-wide association study of diabetic kidney disease in subjects with type 2 diabetesVan Zuydam, N.R.; Ahlqvist, E.; Sandholm, N.; Deshmukh, H.; William Rayner, N.; Abdalla, M.; Ladenvall, C.; Ziemek, D.; Fauman, E.; Robertson, N.R.; McKeigue, P.M.; Valo, E.; Forsblom, C.; Harjutsalo, V.; Perna, A.; Rurali, E.; Loredana Marcovecchio, M.; Igo, R.P.; Salem, R.M.; Perico, N.; et al.
2018Dysphagia in multiple sclerosis: evaluation and validation of the DYMUS questionnaireAlali, D.; Ballard, K.; Vucic, S.; Bogaardt, H.
2018Molecular monitoring in CML: how deep? How often? How should it influence therapy?Shanmuganathan, N.; Hughes, T.P.
2018Diabetic retinopathy in a remote Indigenous primary healthcare population: a Central Australian diabetic retinopathy screening study in the Telehealth Eye and Associated Medical Services Network projectBrazionis, L.; Jenkins, A.; Keech, A.; Ryan, C.; Brown, A.; Boffa, J.; Bursell, S.; CRE in Diabetic Retinopathy and the TEAMSnet Study Group,
2018Empirically derived dietary habits are associated with irritable bowel syndromeZaribaf, F.; Keshteli, A.; Esmaillzadeh, A.; Saneei, P.; Feizi, A.; Daghaghzadeh, H.; Feinle-Bisset, C.; Adibi, P.
2018Impact of gastric emptying and small intestinal transit on blood glucose, intestinal hormones, glucose absorption in the morbidly obeseNguyen, Q.; Debreceni, T.; Burgess, J.; Bellon, M.; Wishart, J.; Standfield, S.; Malbert, C.-H.; Horowitz, M.
2018Association of brain cortical changes with relapse in patients with major depressive disorderZaremba, D.; Dohm, K.; Redlich, R.; Grotegerd, D.; Strojny, R.; Meinert, S.; Bürger, C.; Enneking, V.; Förster, K.; Repple, J.; Opel, N.; Baune, B.; Zwitserlood, P.; Heindel, W.; Arolt, V.; Kugel, H.; Dannlowski, U.
2018Female reproductive and hormonal factors and incidence of primary total knee arthroplasty due to osteoarthritisHussain, S.M.; Wang, Y.; Giles, G.G.; Graves, S.; Wluka, A.E.; Cicuttini, F.M.
2018Bi-allelic recessive loss-of-function variants in FANCM cause non-obstructive azoospermiaKasak, L.; Punab, M.; Nagirnaja, L.; Grigorova, M.; Minajeva, A.; Lopes, A.M.; Punab, A.M.; Aston, K.I.; Carvalho, F.; Laasik, E.; Smith, L.B.; Conrad, D.F.; Laan, M.
2018Integrative genomic analysis reveals cancer-associated mutations at diagnosis of CML in patients with high-risk diseaseBranford, S.; Wang, P.; Yeung, D.T.; Thomson, D.; Purins, A.; Wadham, C.; Shahrin, N.H.; Marum, J.E.; Nataren, N.; Parker, W.T.; Geoghegan, J.; Feng, J.; Shanmuganathan, N.; Mueller, M.C.; Dietz, C.; Stangl, D.; Donaldson, Z.; Altamura, H.; Georgievski, J.; Braley, J.; et al.