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Results 11-20 of 55 (Search time: 0.004 seconds).
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PreviewIssue DateTitleAuthor(s)
2019Genomic subtyping and therapeutic targeting of acute erythroleukemiaIacobucci, I.; Wen, J.; Meggendorfer, M.; Choi, J.K.; Shi, L.; Pounds, S.B.; Carmichael, C.L.; Masih, K.E.; Morris, S.M.; Lindsley, R.C.; Janke, L.J.; Alexander, T.B.; Song, G.; Qu, C.; Li, Y.; Payne-Turner, D.; Tomizawa, D.; Kiyokawa, N.; Valentine, M.; Valentine, V.; et al.
2019Insulin resistance and systemic metabolic changes in oral glucose tolerance test in 5340 individuals: an interventional studyWang, Q.; Jokelainen, J.; Auvinen, J.; Puukka, K.; Keinänen-Kiukaanniemi, S.; Järvelin, M.R.; Kettunen, J.; Mäkinen, V.P.; Ala-Korpela, M.
2021Association of child maltreatment with risk of death during childhood in South AustraliaSegal, L.; Doidge, J.; Armfield, J.M.; Gnanamanickam, E.S.; Preen, D.B.; Brown, D.S.; Nguyen, H.
2014Effects of simulated interventions to improve school entry academic skills on socioeconomic inequalities in educational achievementChittleborough, C.; Mittinty, M.; Lawlor, D.; Lynch, J.
2014Renal replacement therapy associated with lithium nephrotoxicity in AustraliaRoxanas, M.; Grace, B.; George, C.
2011Association between common variation at the FTO locus and changes in body mass index from infancy to late childhood: the complex nature of genetic association through growth and developmentSovio, U.; Mook-Kanamori, D.; Warrington, N.; Lawrence, R.; Briollais, L.; Palmer, C.; Cecil, J.; Sandling, J.; Syvanen, A.; Kaakinen, M.; Beilin, L.; Millwood, I.; Bennett, A.; Laitneen, J.; Pouta, A.; Molitor, J.; Smith, G.; Ben-Shlomo, Y.; Jaddoe, V.; Palmer, L.; et al.; Gibson, G.
2020Global burden of 369 diseases and injuries in 204 countries and territories, 1990–2019: a systematic analysis for the Global Burden of Disease Study 2019GBD 2019 Diseases and Injuries Collaborators,; Baune, B.; Bhandari, D.; Ciobanu, L.; Lalloo, R.; Lassi, Z.; Noubiap Nzeale, J.
2002Economic inequality, working-class power, social capital, and cause-specific mortality in wealthy countriesMuntaner, C.; Lynch, J.W.; Hillemeier, M.; Lee, J.H.; David, R.; Benach, J.; Borrell, C.
2013Identification Of KLHL41 mutations implicates BTB-Kelch-Mediated Ubiquitination as an alternate pathway to myofibrillar disruption in nemaline myopathyGupta, V.; Ravenscroft, G.; Shaheen, R.; Todd, E.; Swanson, L.; Shiina, M.; Ogata, K.; Hsu, C.; Clarke, N.; Darras, B.; Farrar, M.; Hashem, A.; Manton, N.; Muntoni, F.; North, K.; Sandaradura, S.; Nishino, I.; Hayashi, Y.; Sewry, C.; Thompson, E.; et al.
2002The molecular basis of cystathionine b-synthase deficiency in Australian patients: Genotype-phenotype correlations and response to treatmentGaustadnes, M.; Wilcken, B.; Oliveriusova, J.; McGill, J.; Fletcher, J.; Kraus, J.; Wilcken, D.

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