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Showing results (171-180 of 561) with videos related to

Pageof 57
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Journal of Parkinson'S Disease|August 14, 2013
Guided self-help for the management of worry in Parkinson's disease: a pilot studyRachael A Lawson, David Millar, Richard G Brown, et al.
American Journal of Medical Genetics|September 1, 1990
Midline facial defects with ocular colobomataI K Temple, H Brunner, B Jones, et al.
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.
Pageof 57

Showing results (171-180 of 561) with videos related to

Sort By:
Pageof 57
Journal of Parkinson'S Disease|August 14, 2013
Guided self-help for the management of worry in Parkinson's disease: a pilot studyRachael A Lawson, David Millar, Richard G Brown, et al.
American Journal of Medical Genetics|September 1, 1990
Midline facial defects with ocular colobomataI K Temple, H Brunner, B Jones, et al.
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.
Pageof 57