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Acta Neurologica Scandinavica|September 29, 2016
A longitudinal study of the SF-36 version 2 in Friedreich ataxiaG Tai, L A Corben, E M Yiu, et al.Archives of Disease in Childhood|November 23, 2005
Sleep disturbance in Sanfilippo syndrome: a parental questionnaire studyJ Fraser, A A Gason, J E Wraith, et al.Journal of Child Neurology|December 6, 2001
Genetic factors in athetoid cerebral palsyD J Amor, J E Craig, M B Delatycki, et al.Public Health Genomics|January 22, 2010
Population-based genetic screening for cystic fibrosis: attitudes and outcomesL Ioannou, J Massie, V Collins, et al.Clinical Genetics|November 26, 2009
Implementation of ironXS: a study of the acceptability and feasibility of genetic screening for hereditary hemochromatosis in high schoolsM B Delatycki, M Wolthuizen, V Collins, et al.Journal of Medical Ethics|December 2, 2009
Genetic selection for deafness: the views of hearing children of deaf adultsC Mand, R E Duncan, L Gillam, et al.Journal of Community Genetics|May 30, 2013
'No thanks'-reasons why pregnant women declined an offer of cystic fibrosis carrier screeningL Ioannou, J Massie, S Lewis, et al.Clinical Genetics|May 11, 2007
Newborn screening for mucopolysaccharidoses: opinions of patients and their familiesI M Hayes, V Collins, M Sahhar, et al.Neuroscience|September 21, 2010
Successful treatment of auditory perceptual disorder in individuals with Friedreich ataxiaG Rance, L A Corben, E Du Bourg, et al.Journal of Neurology, Neurosurgery, and Psychiatry|October 24, 2006
How is disease progress in Friedreich's ataxia best measured? A study of four rating scalesM C Fahey, L Corben, V Collins, et al.Pageof 12