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J Burn

Showing results (351-360 of 561) with videos related to

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European Journal of Cancer (Oxford, England : 1990)|July 1, 1995
The protocol for a European double-blind trial of aspirin and resistant starch in familial adenomatous polyposis: the CAPP study. Concerted Action Polyposis PreventionJ Burn, P D Chapman, J Mathers, et al.
Neuroscience Letters|May 25, 2010
Genetic variation of CHRNA4 does not modulate attention in Parkinson's diseaseGavin Hudson, Andrea Stutt, Martin Eccles, et al.
Nature Genetics|May 10, 2000
Mutations in TFAP2B cause Char syndrome, a familial form of patent ductus arteriosusM Satoda, F Zhao, G A Diaz, et al.
Journal of Medical Genetics|December 1, 1990
Alagille syndrome and deletion of 20pF Anad, J Burn, D Matthews, et al.
Journal of Medical Genetics|October 1, 1991
The non-deletion type of alpha thalassaemia/mental retardation: a recognisable dysmorphic syndrome with X linked inheritanceA O Wilkie, M E Pembrey, R J Gibbons, et al.
Brain : a Journal of Neurology|June 16, 2001
The prevalence of progressive supranuclear palsy (Steele-Richardson-Olszewski syndrome) in the UKU Nath, Y Ben-Shlomo, R G Thomson, et al.
Acta Gastro-Enterologica Belgica|September 1, 1995
The genetic background of familial adenomatous polyposis. Linkage analysis, the APC gene identification and mutation screeningA Kartheuser, S West, C Walon, et al.
Annals of Neurology|July 17, 1998
Olivopontocerebellar atrophy and multiple system atrophy: clinical follow-up of 10 patients studied with PETA Schrag, J O Rinne, D J Burn, et al.
International Journal of Geriatric Psychiatry|August 15, 2006
Orthostatic hypotension in Parkinson's disease: association with cognitive decline?Liesl M Allcock, Rose Anne Kenny, Urs Peter Mosimann, et al.
Neuroimage|November 6, 2004
The application of statistical parametric mapping to 123I-FP-CIT SPECT in dementia with Lewy bodies, Alzheimer's disease and Parkinson's diseaseSean J Colloby, John T O'Brien, John D Fenwick, et al.
Pageof 57

Showing results (351-360 of 561) with videos related to

Sort By:
Pageof 57
European Journal of Cancer (Oxford, England : 1990)|July 1, 1995
The protocol for a European double-blind trial of aspirin and resistant starch in familial adenomatous polyposis: the CAPP study. Concerted Action Polyposis PreventionJ Burn, P D Chapman, J Mathers, et al.
Neuroscience Letters|May 25, 2010
Genetic variation of CHRNA4 does not modulate attention in Parkinson's diseaseGavin Hudson, Andrea Stutt, Martin Eccles, et al.
Nature Genetics|May 10, 2000
Mutations in TFAP2B cause Char syndrome, a familial form of patent ductus arteriosusM Satoda, F Zhao, G A Diaz, et al.
Journal of Medical Genetics|December 1, 1990
Alagille syndrome and deletion of 20pF Anad, J Burn, D Matthews, et al.
Journal of Medical Genetics|October 1, 1991
The non-deletion type of alpha thalassaemia/mental retardation: a recognisable dysmorphic syndrome with X linked inheritanceA O Wilkie, M E Pembrey, R J Gibbons, et al.
Brain : a Journal of Neurology|June 16, 2001
The prevalence of progressive supranuclear palsy (Steele-Richardson-Olszewski syndrome) in the UKU Nath, Y Ben-Shlomo, R G Thomson, et al.
Acta Gastro-Enterologica Belgica|September 1, 1995
The genetic background of familial adenomatous polyposis. Linkage analysis, the APC gene identification and mutation screeningA Kartheuser, S West, C Walon, et al.
Annals of Neurology|July 17, 1998
Olivopontocerebellar atrophy and multiple system atrophy: clinical follow-up of 10 patients studied with PETA Schrag, J O Rinne, D J Burn, et al.
International Journal of Geriatric Psychiatry|August 15, 2006
Orthostatic hypotension in Parkinson's disease: association with cognitive decline?Liesl M Allcock, Rose Anne Kenny, Urs Peter Mosimann, et al.
Neuroimage|November 6, 2004
The application of statistical parametric mapping to 123I-FP-CIT SPECT in dementia with Lewy bodies, Alzheimer's disease and Parkinson's diseaseSean J Colloby, John T O'Brien, John D Fenwick, et al.
Pageof 57