Browsing by Author Mackay, Mark

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Issue DateTitleAuthor(s)Citation
2017Bell's Palsy in Children (BellPIC): protocol for a multicentre, placebo-controlled randomized trialHort, Jason; Babl, Franz; Barrow, Lisa; Borland, Meredith; Cheek, John; et al, Various; Furyk, Jeremy; Herd, David; Kochar, Amit; Mackay, Mark; Rao, Arjun; Childrens Hospital Westmead: MedicineBell's Palsy in Children (BellPIC): protocol for a multicentre, placebo-controlled randomized trial, BMC Pediatrics, vol.17, 53, 2017,pp 1-11
2016Current methods of haemolysis detection and reporting as a source of risk to patient safety: A narrative reviewBurnett, Leslie; Chesher, Douglas; Badrick, Tony; Braye, Stephen; Gay, Stephanie; Georgiou, Andrew; Lake, Rebecca; Li, Ling; Mackay, Mark; McCaughey, Euan J.; Vecellio, Elia; Westbrook, Johanna; Northern Clinical School: Medicine; Northern Clinical School: MedicineCurrent methods of haemolysis detection and reporting as a source of risk to patient safety: A narrative review, Clinical Biochemist Reviews, vol.37, 4, 2016,pp 143-151
2017Key factors influencing the incidence of hemolysis: a critical appraisal of current evidenceBurnett, Leslie; Chesher, Douglas; Badrick, Tony; Braye, Stephen; Gay, Stephanie; Georgiou, Andrew; Lake, Rebecca; Li, Ling; Mackay, Mark; McCaughey, Euan J.; Vecellio, Elia; Westbrook, Johanna; Northern Clinical School: Medicine; Northern Clinical School: MedicineKey factors influencing the incidence of hemolysis: a critical appraisal of current evidence, Critical Reviews in Clinical Laboratory Sciences, vol.54, 1, 2017,pp 59-72
2013Role of the sodium channel SCN9A in genetic epilepsy with febrile seizures plus and Dravet syndromeBleasel, Andrew; Andermann, Eva; Bellows, Susannah; et al, Various; Farrell, K.; Gill, Deepak S; Harbord, M; Hodgson, Bree; Iona, Xenia; Mackay, Mark; McMahon, Jacinta; Mullen, Saul A; Mulley, John C; Sadleir, Lynette; Sisodiya, Sanyjay; Webster, Richard; Wirrel, Elaine; Deans Unit: (CIPHER)Role of the sodium channel SCN9A in genetic epilepsy with febrile seizures plus and Dravet syndrome, Epilepsia, vol.54, 9, 2013,pp e122-e126
2013Targeted resequencing in epileptic encephalopathies identifies de novo mutations in CHD2 and SYNGAP1Bleasel, Andrew; Afawi, Zaid; Andrade, Danielle M; Berkovic, Samuel F.; Bye, Ann M. E.; Calvert, Sophie; Carvill, Gemma L; Cook, Joseph; Dorschner, Michael O; Freeman, Jeremy L; Gill, D S; Heavin, Sinead; Howell, Katherine B; Khan, Adiba; Kivity, Sara; Korczyn, Amos; Lerman-Sagie, Tally; Lev, Dorit; Møller2, Rikke S; Mackay, Mark; Malone, Stephen; McMahon, Jacinta; Mefford, Heather; O’Roak, Brian J; Rodriguez-Casero, Victoria; Sadleir, Lynette; Scheffer, Ingrid; Shendure, Jay; Stanley, Thorsten; Wallace, Geoffrey; Weaver, Molly; Webster, Richard; Yendle, Simone; Zelnick, Nathanel; Deans Unit: (CIPHER)Targeted resequencing in epileptic encephalopathies identifies de novo mutations in CHD2 and SYNGAP1, Nature Genetics, vol.45, 7, 2013,pp 825-830