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Results 31-40 of 135 (Search time: 0.002 seconds).
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PreviewIssue DateTitleAuthor(s)
2010Characterization of atrial remodeling studied remote from episodes of typical atrial flutterStiles, M.; Wong, C.; John, B.; Kuklik, P.; Brooks, A.; Lau, D.; Dimitri, H.; Wilson, L.; Young, G.; Sanders, P.
2010Human TUBB3 mutations perturb microtubule dynamics, kinesin interactions, and axon guidanceTischfield, M.; Baris, H.; Wu, C.; Rudolph, G.; van Maldergem, L.; He, W.; Chan, W.; Andrews, C.; Demer, J.; Robertson, R.; Mackey, D.; Ruddle, J.; Bird, T.; Gottlob, I.; Pieh, C.; Traboulsi, E.; Pomeroy, S.; Hunter, D.; Soul, J.; Newlin, A.; et al.
2010Characteristics of plasma NOx levels in severe sepsis: High interindividual variability and correlation with illness severity, but lack of correlation with cortisol levelsHo, J.; Chapman, M.; O'Connor, S.; Lam, S.; Edwards, J.; Ludbrook, G.; Lewis, J.; Torpy, D.
2010Circulating levels of TWEAK correlate with bone erosion in multiple myeloma patientsWilliams, S.; Martin, S.; Vincent, C.; Gronthos, S.; Zheng, T.; Atkins, G.; Zannettino, A.
2010The effects of high-dose esomeprazole on gastric and oesophageal acid exposure and molecular markers in Barrett's oesophagusAbu-Sneineh, A.; Tam, W.; Schoeman, M.; Fraser, R.; Ruszkiewicz, A.; Smith, E.; Drew, P.; Dent, J.; Holloway, R.
2010Poor prognosis in familial acute myeloid leukaemia with combined biallelic CEBPA mutations and downstream events affecting the ATM, FLT3 and CDX2 genesCarmichael, C.; Wilkins, E.; Bengtsson, H.; Horwitz, M.; Speed, T.; Vincent, P.; Young, G.; Hahn, C.; Escher, J.; Scott, H.
2010Subclinical Cushing's syndrome in adrenal incidentaloma: a common problem or an artefact of current diagnostic testing?Gagliardi, L.; Torpy, D.
2010High cortisol levels in hyperglycaemic myocardial infarct patients signify stress hyperglycaemia and predict subsequent normalization of glucose toleranceWong, K.; Wong, V.; Ho, J.; Torpy, D.; McLean, M.; Cheung, N.
2010B cell-intrinsic signaling through IL-21 receptor and STAT3 is required for establishing long-lived antibody responses in humansAvery, D.; Deenick, E.; Ma, C.; Suryani, S.; Simpson, N.; Chew, G.; Chan, T.; Palendira, U.; Bustamante, J.; Boisson-Dupuis, S.; Choo, S.; Bleasel, K.; Peake, J.; King, C.; French, M.; Engelhard, D.; Al-Hajjar, S.; Al-Muhsen, S.; Magdorf, K.; Roesler, J.; et al.
2010Novel RUNX1 mutations in familial platelet disorder with enhanced risk for acute myeloid leukemia: clues for improved identification of the FPD/AML syndromeJongmans, M.; Kuiper, R.; Carmichael, C.; Wilkins, E.; Dors, N.; Carmagnac, A.; Schouten-van Meeteren, N.; Li, X.; Stankovic, M.; Kamping, E.; Bengtsson, H.; Schoenmakers, M.; Geurts van Kessel, A.; Hoogerbrugge, P.; Hahn, C.; Brons, P.; Scott, H.; Hoogerbrugge, N.

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