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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 study
Rachael A Lawson, David Millar, Richard G Brown, et al.
American Journal of Medical Genetics
|
September 1, 1990
Midline facial defects with ocular colobomata
I 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 disease
Nick 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 transcript
T Hamzehloei, S P West, P Chapman, et al.
Headache
|
March 1, 1993
An association between migrainous aura and hereditary haemorrhagic telangiectasia
J 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 disease
L 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 bodies
S 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 phenotype
A Curtis, R Nelson, M Porteous, et al.
Journal of Medical Genetics
|
August 3, 2000
Autosomal dominant sacral agenesis: Currarino syndrome
S A Lynch, Y Wang, T Strachan, et al.
Page
of 57
Search research articles
Search
Showing results (171-180 of 561) with videos related to
Sort By:
Page
of 57
Journal of Parkinson'S Disease
|
August 14, 2013
Guided self-help for the management of worry in Parkinson's disease: a pilot study
Rachael A Lawson, David Millar, Richard G Brown, et al.
American Journal of Medical Genetics
|
September 1, 1990
Midline facial defects with ocular colobomata
I 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 disease
Nick 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 transcript
T Hamzehloei, S P West, P Chapman, et al.
Headache
|
March 1, 1993
An association between migrainous aura and hereditary haemorrhagic telangiectasia
J 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 disease
L 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 bodies
S 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 phenotype
A Curtis, R Nelson, M Porteous, et al.
Journal of Medical Genetics
|
August 3, 2000
Autosomal dominant sacral agenesis: Currarino syndrome
S A Lynch, Y Wang, T Strachan, et al.
Page
of 57