Showing results (151-160 of 571) with videos related to
Sort By:
Pageof 58
Clinical Rehabilitation|December 20, 2007
How do I sound to me? Perceived changes in communication in Parkinson's diseaseNick Miller, Emma Noble, Diana Jones, et al.Molecular and Cellular Probes|October 1, 1996
Mutation detection in exons 1-14 of the adenomatous polyposis coli gene: identification of an alternatively spliced transcriptT Hamzehloei, S P West, P Chapman, et al.Headache|March 1, 1993
An association between migrainous aura and hereditary haemorrhagic telangiectasiaJ G Steele, P U Nath, J Burn, et al.Journal of Neurology, Neurosurgery, and Psychiatry|September 21, 2004
Frequency of orthostatic hypotension in a community based cohort of patients with Parkinson's diseaseL M Allcock, K Ullyart, R A Kenny, et al.Clinical Dysmorphology|April 1, 1997
Absent nails, kinesogenic choreoathetosis, epilepsy and developmental delay--a new autosomal dominant disorder?S A Lynch, D Gardner-Medwin, J Burn, et al.Journal of Neurology, Neurosurgery, and Psychiatry|August 19, 2005
The role of levodopa in the management of dementia with Lewy bodiesS Molloy, I G McKeith, J T O'Brien, et al.Journal of Medical Genetics|January 1, 1991
Association of less common cystic fibrosis mutations with a mild phenotypeA Curtis, R Nelson, M Porteous, et al.Journal of Medical Genetics|August 3, 2000
Autosomal dominant sacral agenesis: Currarino syndromeS A Lynch, Y Wang, T Strachan, et al.International Journal of Colorectal Disease|April 21, 1998
Hereditary non-polyposis colorectal cancerS E Green, D M Bradburn, J S Varma, et al.Journal of the Royal College of Physicians of London|January 1, 1992
Carrier testing for cystic fibrosis: knowledge and attitudes within a local communityD Magnay, O Wilson, S el Hait, et al.Pageof 58