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Journal of Medical Genetics
|
May 1, 1988
Exclusion of calcitonin as a candidate gene for the basic defect in a family with autosomal dominant supravalvular aortic stenosis
C P Bennett, J Burn, G E Moore, et al.
The British Journal of Surgery
|
October 1, 1995
Clinical impact of colonoscopic screening in first-degree relatives of patients with hereditary non-polyposis colorectal cancer
S E Green, P D Chapman, J Burn, et al.
Parkinson'S Disease
|
June 1, 2018
Coping with Cognitive Impairment in People with Parkinson's Disease and Their Carers: A Qualitative Study
Rachael A Lawson, Daniel Collerton, John-Paul Taylor, et al.
Gut
|
November 4, 2008
Cell kinetics and gene expression changes in colorectal cancer patients given resistant starch: a randomised controlled trial
S S Dronamraju, J M Coxhead, S B Kelly, et al.
Neurology
|
March 26, 2003
Clinical features and natural history of progressive supranuclear palsy: a clinical cohort study
U Nath, Y Ben-Shlomo, R G Thomson, et al.
Journal of Medical Genetics
|
December 1, 1994
Genetic heterogeneity in hereditary haemorrhagic telangiectasia
M E Porteous, A Curtis, O Williams, et al.
Annals of the Royal College of Surgeons of England
|
June 17, 2025
Impact of COVID-19 on management and outcomes of NHS patients with recurrent respiratory papillomatosis: evidence from a UK registry
A Donne, K Keltie, P Cognigni, et al.
Annals of Neurology
|
August 2, 2003
Increased Alzheimer pathology in Parkinson's disease related to antimuscarinic drugs
Elaine K Perry, Linda Kilford, Andrew J Lees, et al.
The British Journal of Ophthalmology
|
October 1, 1986
Warburg (HARD +/- E) syndrome without retinal dysplasia: case report and review
M F Attia, J Burn, J H McCarthy, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
February 9, 2002
Late-onset axial jerky dystonia due to the DYT1 deletion
Patrick F Chinnery, Paul J Reading, Emma L McCarthy, et al.
Page
of 57
Search research articles
Search
Showing results (231-240 of 561) with videos related to
Sort By:
Page
of 57
Journal of Medical Genetics
|
May 1, 1988
Exclusion of calcitonin as a candidate gene for the basic defect in a family with autosomal dominant supravalvular aortic stenosis
C P Bennett, J Burn, G E Moore, et al.
The British Journal of Surgery
|
October 1, 1995
Clinical impact of colonoscopic screening in first-degree relatives of patients with hereditary non-polyposis colorectal cancer
S E Green, P D Chapman, J Burn, et al.
Parkinson'S Disease
|
June 1, 2018
Coping with Cognitive Impairment in People with Parkinson's Disease and Their Carers: A Qualitative Study
Rachael A Lawson, Daniel Collerton, John-Paul Taylor, et al.
Gut
|
November 4, 2008
Cell kinetics and gene expression changes in colorectal cancer patients given resistant starch: a randomised controlled trial
S S Dronamraju, J M Coxhead, S B Kelly, et al.
Neurology
|
March 26, 2003
Clinical features and natural history of progressive supranuclear palsy: a clinical cohort study
U Nath, Y Ben-Shlomo, R G Thomson, et al.
Journal of Medical Genetics
|
December 1, 1994
Genetic heterogeneity in hereditary haemorrhagic telangiectasia
M E Porteous, A Curtis, O Williams, et al.
Annals of the Royal College of Surgeons of England
|
June 17, 2025
Impact of COVID-19 on management and outcomes of NHS patients with recurrent respiratory papillomatosis: evidence from a UK registry
A Donne, K Keltie, P Cognigni, et al.
Annals of Neurology
|
August 2, 2003
Increased Alzheimer pathology in Parkinson's disease related to antimuscarinic drugs
Elaine K Perry, Linda Kilford, Andrew J Lees, et al.
The British Journal of Ophthalmology
|
October 1, 1986
Warburg (HARD +/- E) syndrome without retinal dysplasia: case report and review
M F Attia, J Burn, J H McCarthy, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
February 9, 2002
Late-onset axial jerky dystonia due to the DYT1 deletion
Patrick F Chinnery, Paul J Reading, Emma L McCarthy, et al.
Page
of 57