Browsing by Author Fahey, Michael

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Issue DateTitleAuthor(s)Citation
2015Alemtuzumab treatment of multiple sclerosis: long-term safety and efficacyHill-Cawthorne, Grant; Azzopardi, Laura; Bjornson, Ingunn; Button, Tom; Coles, Alasdair; Compston, Alastair; Costelloe, Lisa; Fahey, Michael; Harding, Katherine; Jones, Joanne; Kousin-Ezewu, Onajite; May, Karen; Robertson, Neil; Tuohy, Orla; School of Public Health: Public HealthAlemtuzumab treatment of multiple sclerosis: long-term safety and efficacy, Journal of Neurology, Neurosurgery, and Psychiatry, vol.86, 2, 2015,pp 208-215
2009Ascorbic acid for Charcot-Marie-Tooth disease type 1A in children: a randomised, double-blind, placebo-controlled, safety and efficacy trialBurns, Joshua; Ouvrier, Robert; Fahey, Michael; Joseph, Pathma; Kornberg, Andrew J.; Ryan, Monique; Yiu, Eppie M.; Clinical and Rehabilitation Sciences; Children's Hospital Westmead: Paediatrics & Child HealthAscorbic acid for Charcot-Marie-Tooth disease type 1A in children: a randomised, double-blind, placebo-controlled, safety and efficacy trial, Lancet Neurology, vol.8, 6, 2009,pp 537-544
2008Mutations in TPM3 are a common cause of congenital fiber type disproportionClarke, Nigel; North, Kathryn; Bellance, Remi; Dye, Danielle; Fahey, Michael; Johnson, Edward; Kolski, Hanna; Labarre-Vila, Annick; Laing, Nigel G.; Lim, Esther; Monnier, Nicole; Patel, Rakesh; Romero, Norma; Smith, Robert; Children's Hospital Westmead: Paediatrics & Child Health; Children's Hospital Westmead: Paediatrics & Child HealthMutations in TPM3 are a common cause of congenital fiber type disproportion, Annals of Neurology, vol.63,(3),2008,pp 329-337