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Page 1
Homozygous lamin A/C familial lipodystrophy R482Q mutation in autosomal recessive Emery Dreifuss muscular dystrophy.
Wiltshire KM, Hegele RA, Innes AM, Brownell AK. Wiltshire KM, et al. Neuromuscul Disord. 2013 Mar;23(3):265-8. doi: 10.1016/j.nmd.2012.11.011. Epub 2013 Jan 11. Neuromuscul Disord. 2013. PMID: 23313286
The incidence and prevalence of Huntington's disease: a systematic review and meta-analysis.
Pringsheim T, Wiltshire K, Day L, Dykeman J, Steeves T, Jette N. Pringsheim T, et al. Mov Disord. 2012 Aug;27(9):1083-91. doi: 10.1002/mds.25075. Epub 2012 Jun 12. Mov Disord. 2012. PMID: 22692795 Review.
Corpus callosum in neurodegenerative diseases: findings in Parkinson's disease.
Wiltshire K, Foster S, Kaye JA, Small BJ, Camicioli R. Wiltshire K, et al. Dement Geriatr Cogn Disord. 2005;20(6):345-51. doi: 10.1159/000088526. Epub 2005 Sep 26. Dement Geriatr Cogn Disord. 2005. PMID: 16192724
Asphyxiation causing distinctive basal ganglia injury and generalized dystonia.
Wiltshire KM, Myers K, Wei XC, Mohamed I. Wiltshire KM, et al. Can J Neurol Sci. 2011 May;38(3):514-5. doi: 10.1017/s0317167100011963. Can J Neurol Sci. 2011. PMID: 21515515 No abstract available.
Neuronal Intranuclear Inclusion Disease presenting as juvenile Parkinsonism.
Wiltshire KM, Dunham C, Reid S, Auer RN, Suchowersky O. Wiltshire KM, et al. Can J Neurol Sci. 2010 Mar;37(2):213-8. doi: 10.1017/s031716710000994x. Can J Neurol Sci. 2010. PMID: 20437931
Corpus callosum and cingulum tractography in Parkinson's disease.
Wiltshire K, Concha L, Gee M, Bouchard T, Beaulieu C, Camicioli R. Wiltshire K, et al. Can J Neurol Sci. 2010 Sep;37(5):595-600. doi: 10.1017/s0317167100010751. Can J Neurol Sci. 2010. PMID: 21059504
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