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| Preview | Issue Date | Title | Author(s) |
| 2012 | Dairy food intake of Australian children and adolescents 2-16 years of age: 2007 Australian National Children's Nutrition and Physical Activity Survey | Baird, D.; Syrette, J.; Hendrie, G.; Riley, M.; Bowen, J.; Noakes, M. |
| 2009 | Damaging effects of chronic low-dose methotrexate usage on primary bone formation in young rats and potential protective effects of folinic acid supplementary treatment | Fan, C.; Cool, J.; Scherer, M.; Foster, B.; Shandala, T.; Tapp, H.; Xian, C. |
| 2020 | Data integrity of 35 randomised controlled trials in women’ health | Bordewijk, E.M.; Wang, R.; Askie, L.M.; Gurrin, L.C.; Thornton, J.G.; van Wely, M.; Li, W.; Mol, B.W. |
| 2008 | Day 4 embryo selection is equal to Day 5 using a new embryo scoring system validated in single embryo transfers | Inglis, D.; Henshaw, R.; Lane, M. |
| 2014 | Day differences in the cortisol awakening response predict day differences in synaptic plasticity in the brain | Clow, A.; Law, R.; Evans, P.; Vallence, A.M.; Hodyl, N.A.; Goldsworthy, M.R.; Rothwell, J.R.; Ridding, M.C. |
| 1999 | Daytime melatonin and temazepam in young adult humans: equivalent effects on sleep latency and body temperatures | Gilbert, S. S.; van den Heuvel, Cameron Jay; Dawson, Drew |
| 2013 | De novo intragenic deletion of the autism susceptibility candidate 2 (AUTS2) gene in a patient with developmental delay: A case report and literature review | Jolley, A.; Corbett, M.; McGregor, L.; Waters, W.; Brown, S.; Nicholl, J.; Yu, S. |
| 2016 | De novo loss-of-function mutations in USP9X cause a female-specific recognizable syndrome with developmental delay and congenital malformations | Reijnders, M.; Zachariadis, V.; Latour, B.; Jolly, L.; Mancini, G.; Pfundt, R.; Wu, K.; Van Ravenswaaij-Arts, C.; Veenstra-Knol, H.; Anderlid, B.; Wood, S.; Cheung, S.; Barnicoat, A.; Probst, F.; Magoulas, P.; Brooks, A.; Malmgren, H.; Harila-Saari, A.; Marcelis, C.; Vreeburg, M.; et al. |
| 2004 | De novo mutations in the mitochondrial ND3 gene as a cause of infantile mitochondrial encephalopathy and complex I deficiency | McFarland, R.; Kirby, D.; Fowler, K.; Ohtake, A.; Ryan, M.; Amor, D.; Fletcher, J.; Dixon, J.; Collins, F.; Turnbull, D.; Taylor, R.; Thorburn, A. |
| 2010 | De novo mutations of SETBP1 cause Schinzel-Giedion syndrome | Hoischen, A.; Van Bon, B.; Gilissen, C.; Arts, P.; van Lier, B.; Steehouwer, M.; de Vries, P.; de Reuver, R.; Wieskamp, N.; Mortier, G.; Devriendt, K.; Amorim, M.; Revencu, N.; Kidd, A.; Barbosa, M.; Turner, A.; Smith, J.; Olay, C.; Henderson, A.; Hayes, I.; et al. |
| 2010 | De novo SCN1A mutations in Dravet syndrome and related epileptic encephalopathies are largely of paternal origin | Heron, S.; Scheffer, I.; Iona, X.; Zuberi, S.; Birch, R.; McMahon, J.; Bruce, C.; Berkovic, S.; Mulley, J. |
| 2011 | De novo SCN1A mutations in migrating partial seizures of infancy | Carranza Rojo, D.; Hamiwka, L.; McMahon, J.; Dibbens, L.; Arsov, T.; Suls, A.; Stodberg, T.; Kelley, K.; Wirrell, E.; Appleton, B.; Mackay, M.; Freeman, J.; Yendle, S.; Berkovic, S.; Bienvenu, T.; De Jonghe, P.; Thorburn, D.; Mulley, J.; Mefford, H.; Scheffer, I. |
| 2015 | Dealing with the unknown: reducing the proportion of unvalidated treatments offered to children | Wilkinson, D.; Chalmers, I.; Cruz, M.; Tarnow-Mordi, W. |
| 2006 | Death in the neonatal intensive care unit: changing patterns of end of life care over two decades | Wilkinson, D.; Fitzsimons, J.; Dargaville, P.; Campbell, N.; Loughnan, P.; McDougall, P.; Mils, J. |
| 2009 | Death in the Netherlands: evidence and argument | Wilkinson, D. |
| 2013 | Death or disability?: the 'Carmentis machine' and decision-making for critically ill children | Wilkinson, D. |
| 2016 | Death talk: Basic linguistic rules and communication in perinatal and paediatric end-of-life discussions | Xafis, V.; Watkins, A.; Wilkinson, D. |
| 2013 | Debate: idiopathic short stature should be treated with growth hormone | Ambler, G.; Fairchild, J.; Wilkinson, D. |
| 2013 | Decellularized feeders: an optimized method for culturing pluripotent cells | Lim, M.; Jungebluth, P.; Sjoqvist, S.; Nidkin, H.; Kjartansdottir, K.; Unger, C.; Vassiliev, I.; Macchiarini, P. |
| 2013 | Deciphering the mechanistic pathways of the instant blood mediated inflammatory reaction against porcine neonatal islet cells | Liuwantara, D.; Phillips, P.; Favaloro, E.; Salvaris, E.J.; Hawkes, J.; Brady, J.; Lew, A.M.; Nottle, M.B.; d'Apice, A.J.; Cowan, P.J.; O'Connell, P.J.; Hawthorne, W.J.; Joint Congress of IXA and Organ Transplantation in ABO-incompatible and Hyperimmunized Recipients (IXA 2013) (10 Nov 2013 - 13 Nov 2013 : Osaka, Japan) |
