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2007 Journal Article Clinical features and natural history of neuroferritinopathy caused by the FTL1 460InsA mutationChinnery, PF, Crompton, DE, Birchall, D, Jackson, MJ, Coulthard, A, Lombes, A, Quinn, N, Wills, A, Fletcher, N, Mottershead, JP, Cooper, P, Kellett, M, Bates, D and Burn, J (2007). Clinical features and natural history of neuroferritinopathy caused by the FTL1 460InsA mutation. Brain, 130 (1), 110-119. doi: 10.1093/brain/awl319 |
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2007 Journal Article Observational analytic studies in multiple sclerosis: controlling bias through study design and conduct. The Australian Multicentre Study of Environment and Immune FunctionLucas, R. M., Ponsonby, A. L., McMichael, A. J., van der Mei, I., Chapman, C., Coulthard, A., Dear, K., Dwyer, T., Kilpatrick, T. J., Pender, M. P., Taylor, B., Valery, P. and Williams, D. (2007). Observational analytic studies in multiple sclerosis: controlling bias through study design and conduct. The Australian Multicentre Study of Environment and Immune Function. Multiple Sclerosis, 13 (7), 827-839. doi: 10.1177/1352458507077174 |
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2004 Journal Article Double-Blind, Placebo-Controlled Trial of Octreotide Long-Acting Repeatable (LAR) in Thyroid-Associated OphthalmopathyDickinson, A. Jane, Vaidya, Bijay, Miller, Margaret, Coulthard, Alan, Perros, Petris, Baister, Elizabeth, Andrews, Christopher D., Hesse, Lutz, Heverhagen, Johannes T., Heufelder, Armin E. and Kendall-Taylor, Pat (2004). Double-Blind, Placebo-Controlled Trial of Octreotide Long-Acting Repeatable (LAR) in Thyroid-Associated Ophthalmopathy. Journal of Clinical Endocrinology and Metabolism, 89 (12), 5910-5915. doi: 10.1210/jc.2004-0697 |
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2004 Journal Article Identification of a mutation in synapsin I, a synaptic vesicle protein, in a family with epilepsyGarcia, C. C, Blair, H. J., Seager, M., Coulthard, A., Tennant, S., Buddles, M., Curtis, A. and Goodship, J. A. (2004). Identification of a mutation in synapsin I, a synaptic vesicle protein, in a family with epilepsy. Journal of Medical Genetics, 41 (3), 183-186. doi: 10.1136/jmg.2003.013680 |
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2003 Journal Article Neuroferritinopathy in a French family with late onset dominant dystoniaChinnery, P. F., Curtis, A. R. J., Fey, C., Coulthard, A., Crompton, D., Curtis, A., Lombés, A. and Burn, J. (2003). Neuroferritinopathy in a French family with late onset dominant dystonia. Journal of Medical Genetics, 40 (5), e69.1-e.69.3. doi: 10.1136/jmg.40.5.e69 |
