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Quality of Life Research : an International Journal of Quality of Life Aspects of Treatment, Care and Rehabilitation|November 5, 2016
Can in-the-moment diary methods measure health-related quality of life in Duchenne muscular dystrophy?Paula Bray, Anita C Bundy, Monique M Ryan, et al.Clinical Genetics|November 7, 2019
Cerebellar ataxia with normal intellect associated with a homozygous truncating variant in CA8Christopher M Richmond, Richard Leventer, Monique M Ryan, et al.Journal of Paediatrics and Child Health|April 21, 2007
Spinal muscular atrophy type 1: is long-term mechanical ventilation ethical?Monique M Ryan, Henry Kilham, Stephen Jacobe, et al.Journal of Paediatrics and Child Health|August 24, 2006
Juvenile Huntington diseaseNimeshan Geevasinga, Fiona H Richards, Kristi J Jones, et al.Physical & Occupational Therapy in Pediatrics|February 23, 2010
Feasibility of a computerized method to measure quality of "everyday" life in children with neuromuscular disordersPaula Bray, Anita C Bundy, Monique M Ryan, et al.Journal of the Peripheral Nervous System : JPNS|October 11, 2008
Neurophysiologic abnormalities in children with Charcot-Marie-Tooth disease type 1AEppie M Yiu, Joshua Burns, Monique M Ryan, et al.Pediatric Neurology|October 24, 2007
Concomitant transverse myelitis and acute motor axonal neuropathy in an adolescentKatherine B Howell, Jithangi Wanigasinghe, Richard J Leventer, et al.American Journal of Medical Genetics. Part A|August 5, 2010
Atypical Silver-Russell phenotype resulting from maternal uniparental disomy of chromosome 7Zornitza Stark, Monique M Ryan, Damien L Bruno, et al.Journal of Human Nutrition and Dietetics : the Official Journal of the British Dietetic Association|December 22, 2021
The association between dietary factors and body weight and composition in boys with Duchenne muscular dystrophyNatassja Billich, Maureen Evans, Helen Truby, et al.Neuromuscular Disorders : NMD|December 15, 2022
Correlation between whole body muscle MRI and functional measures in paediatric patients with facioscapulohumeral muscular dystrophyIan R Woodcock, Katy de Valle, Nisha Varma, et al.Pageof 16