Emeritus Professor David BatesEmeritus Professor
Email: david.bates@ncl.ac.uk Telephone: +44 (0) 191 282 4949 Fax: +44 (0) 191 261 0881 Address: Department of Neurology
Bates D, Bartholome E. Treatment effect of natalizumab on relapse outcomes in multiple sclerosis patients despite ongoing MRI activity .
Journal of Neurology, Neurosurgery and Psychiatry 2012, 83 (1), 55-60.
Denys P, Bates D, Burks J, Chancellor M, Signori M, Globe D, Fitz-Randolph M, Hudgens S. Methodology and validation of urinary incontinence in multiple sclerosis screening tool .
In: European Journal of Neurology: 15th Congress of the European Federation of Neurological Societies (EFNS) . 2011, Budapest, Hungary: Wiley-Blackwell Publishing Ltd.
Bates D, Comi G. The way forward to treatment optimisation in multiple sclerosis: Introduction .
Journal of Neurology, Supplement 2004, 251 (s5), V/2.
Powell H, Archibald K, Mountford R, Lynch SA, Bates D, Curtis A. A deletion within the frataxin gene, combined with a GAA expansion mutation causes atypical Friedreich ataxia .
In: Journal of Medical Genetics: British Human Genetics Conference . 2003, York, UK: BMJ Group.
Dalton C, Barker G, MacManus D, Miszkiel K, Bates D, Blumhardt L, Hawkins C, Palace J, Sharief M, Swingler R, Young C, Miller D, Int Natalizumab MS Trial Grp. The effectiveness of Natalizumab on MRI outcome measures in patients with relapsing multiple sclerosis .
In: Journal of Neurology, Neurosurgery and Psychiatry: Joint Congress of the Association of British Neurologists/British Neuropsychiatry Association . 2003, London, UK: BMJ Group.
Curtis ARJ, Fey C, Morris CM, Bindoff LA, Ince PG, Chinnery PF, Coulthard A, Jackson MJ, Jackson AP, McHale DP, Hay D, Barker WA, Markham AF, Bates D, Curtis A, Burn J. Mutation in ferritin light chain causes dominant adult onset neurodegeneration .
Nature Genetics 2001, 28 (4), 350-354.
Bates D. The prognosis of medical coma .
Journal of Neurology, Neurosurgery and Psychiatry 2001, 71 (s1), 20-23.
Burn J, Curtis AR, Bindoff L, Ince P, Coulthard A, Jackson A, Jackson M, Fey C, Hay D, Shepherd D, Bates D, Curtis A. A novel autosomal dominant basal ganglia degeneration with cavitation on 19q can mimic Parkinson's disease and Huntington's disease .
American Journal of Human Genetics 2000, 67 (4), 371-371.
Nodder D, Chappell B, Bates D, Freeman J, Hatch J, Keen J, Thomas S, Young C. Multiple sclerosis: care needs for 2000 and beyond .
Journal of the Royal Society of Medicine 2000, 93 (5), 219-224.
