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PreviewIssue DateTitleAuthor(s)
2016Association of maternal diabetes/glycosuria and pre-pregnancy body mass index with offspring indicators of non-alcoholic fatty liver diseasePatel, S.; Lawlor, D.; Callaway, M.; Macdonald-Wallis, C.; Sattar, N.; Fraser, A.
2015Five-year survival of children with chronic critical illness in Australia and New ZealandNamachivayam, S.; Alexander, J.; Slater, A.; Millar, J.; Erickson, S.; Tibballs, J.; Festa, M.; Ganu, S.; Segedin, L.; Schlapbach, L.; Williams, G.; Shann, F.; Butt, W.
2015A study of the clinical and radiological features in a cohort of 93 patients with a COL2A1 mutation causing spondyloepiphyseal dysplasia congenita or a related phenotypeTerhal, P.; Nievelstein, R.; Verver, E.; Topsakal, V.; van Dommelen, P.; Hoornaert, K.; Le Merrer, M.; Zankl, A.; Simon, M.; Smithson, S.; Marcelis, C.; Kerr, B.; Clayton-Smith, J.; Kinning, E.; Mansour, S.; Elmslie, F.; Goodwin, L.; van der Hout, A.; Veenstra-Knol, H.; Herkert, J.; et al.
2011A lipidomic screen of palmitate-treated MIN6 β-cells links sphingolipid metabolites with endoplasmic reticulum (ER) stress and impaired protein traffickingBoslem, E.; Macintosh, G.; Preston, A.; Bartley, C.; Busch, A.; Fuller, M.; Laybutt, D.; Meikle, P.; Biden, T.
2018The multifaceted presentation of chronic recurrent multifocal osteomyelitis: a series of 486 cases from the Eurofever international registryGirschick, H.; Finetti, M.; Orlando, F.; Schalm, S.; Insalaco, A.; Ganser, G.; Nielsen, S.; Herlin, T.; Koné-Paut, I.; Martino, S.; Cattalini, M.; Anton, J.; Al-Mayouf, S.; Hofer, M.; Quartier, P.; Boros, C.; Kuemmerle-Deschner, J.; Pires Marafon, D.; Alessio, M.; Schwarz, T.; et al.
2014Associations of circulating calcium and 25-hydroxyvitamin D with glucose metabolism in pregnancy: a cross-sectional study in European and south Asian womenWhitelaw, D.; Scally, A.; Tuffnell, D.; Davies, T.; Fraser, W.; Bhopal, R.; Wright, J.; Lawlor, D.
2015High incidence of Noonan Syndrome features including short stature and pulmonic stenosis in patients carrying NF1 missense mutations affecting p.Arg1809: genotype-phenotype correlationRojnueangnit, K.; Xie, J.; Gomes, A.; Sharp, A.; Callens, T.; Chen, Y.; Liu, Y.; Cochran, M.; Abbott, M.; Atkin, J.; Babovic-Vuksanovic, D.; Barnett, C.; Crenshaw, M.; Bartholomew, D.; Basel, L.; Bellus, G.; Ben-Shachar, S.; Bialer, M.; Bick, D.; Blumberg, B.; et al.
2014Outcomes of repair of complete atrioventricular septal defect in the current eraXie, O.; Brizard, C.; D'udekem, Y.; Galati, J.; Kelly, A.; Yong, M.; Weintraub, R.; Konstantinov, I.
2015Evaluation of multiple putative risk alleles within the 15q13.3 region for genetic generalized epilepsyDamiano, J.; Mullen, S.; Hildebrand, M.; Bellows, S.; Lawrence, K.; Arsov, T.; Dibbens, L.; Major, H.; Dahl, H.; Mefford, H.; Darbro, B.; Scheffer, I.; Berkovic, S.
2015Five-year antibody persistence and safety after a single dose of combined Haemophilus influenzae Type B Neisseria meningitidis Serogroup C-tetanus toxoid conjugate vaccine in Haemophilus influenzae Type B-primed toddlersBooy, R.; Nolan, T.; Reynolds, G.; Richmond, P.; Nissen, M.; Marshall, H.; Stoney, T.; Van Der Wielen, M.; Kolhe, D.; Miller, J.