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S G KNIGHT

Showing results (11-20 of 41) with videos related to

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BMC Medical Genetics|September 14, 2013
Splice site SNPs of phospholipase PLCXD3 are significantly associated with variant and sporadic Creutzfeldt-Jakob diseaseMatthew T Bishop, Pascual Sanchez-Juan, Richard S G Knight
BMC Medical Genetics|April 23, 2008
Cathepsin D SNP associated with increased risk of variant Creutzfeldt-Jakob diseaseMatthew T Bishop, Gabor G Kovacs, Pascual Sanchez-Juan, et al.
BMJ (Clinical Research Ed.)|July 13, 2002
vCJD: the epidemic that never was. New variant Creutzfeldt-Jakob disease: the critique that never wasR G Will, R S G Knight, H J T Ward, et al.
Neurology|April 9, 2008
Systematic review of therapeutic interventions in human prion diseaseLesley A Stewart, Larysa H M Rydzewska, Geraldine F Keogh, et al.
Transfusion|August 12, 2011
Sporadic Creutzfeldt-Jakob disease and risk of blood transfusion in the United KingdomAnna M Molesworth, Jan Mackenzie, Dawn Everington, et al.
Electrophoresis|September 5, 2002
Apolipoprotein E and other cerebrospinal fluid proteins differentiate ante mortem variant Creutzfeldt-Jakob disease from ante mortem sporadic Creutzfeldt-Jakob diseaseLeila H Choe, Alison Green, Richard S G Knight, et al.
BMC Medical Genetics|December 29, 2009
PRNP variation in UK sporadic and variant Creutzfeldt Jakob disease highlights genetic risk factors and a novel non-synonymous polymorphismMatthew T Bishop, Catherine Pennington, Craig A Heath, et al.
The British Journal of Ophthalmology|September 20, 2005
Isolated visual symptoms at onset in sporadic Creutzfeldt-Jakob disease: the clinical phenotype of the "Heidenhain variant"S A Cooper, K L Murray, C A Heath, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|July 13, 2006
Sporadic Creutzfeldt-Jakob disease with cerebellar ataxia at onset in the UKS A Cooper, K L Murray, C A Heath, et al.
Neuroscience Letters|May 2, 2002
14-3-3 in the cerebrospinal fluid of patients with variant and sporadic Creutzfeldt-Jakob disease measured using capture assay able to detect low levels of 14-3-3 proteinAlison J E Green, Sanja Ramljak, Werner E G Müller, et al.
Pageof 5

Showing results (11-20 of 41) with videos related to

Sort By:
Pageof 5
BMC Medical Genetics|September 14, 2013
Splice site SNPs of phospholipase PLCXD3 are significantly associated with variant and sporadic Creutzfeldt-Jakob diseaseMatthew T Bishop, Pascual Sanchez-Juan, Richard S G Knight
BMC Medical Genetics|April 23, 2008
Cathepsin D SNP associated with increased risk of variant Creutzfeldt-Jakob diseaseMatthew T Bishop, Gabor G Kovacs, Pascual Sanchez-Juan, et al.
BMJ (Clinical Research Ed.)|July 13, 2002
vCJD: the epidemic that never was. New variant Creutzfeldt-Jakob disease: the critique that never wasR G Will, R S G Knight, H J T Ward, et al.
Neurology|April 9, 2008
Systematic review of therapeutic interventions in human prion diseaseLesley A Stewart, Larysa H M Rydzewska, Geraldine F Keogh, et al.
Transfusion|August 12, 2011
Sporadic Creutzfeldt-Jakob disease and risk of blood transfusion in the United KingdomAnna M Molesworth, Jan Mackenzie, Dawn Everington, et al.
Electrophoresis|September 5, 2002
Apolipoprotein E and other cerebrospinal fluid proteins differentiate ante mortem variant Creutzfeldt-Jakob disease from ante mortem sporadic Creutzfeldt-Jakob diseaseLeila H Choe, Alison Green, Richard S G Knight, et al.
BMC Medical Genetics|December 29, 2009
PRNP variation in UK sporadic and variant Creutzfeldt Jakob disease highlights genetic risk factors and a novel non-synonymous polymorphismMatthew T Bishop, Catherine Pennington, Craig A Heath, et al.
The British Journal of Ophthalmology|September 20, 2005
Isolated visual symptoms at onset in sporadic Creutzfeldt-Jakob disease: the clinical phenotype of the "Heidenhain variant"S A Cooper, K L Murray, C A Heath, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|July 13, 2006
Sporadic Creutzfeldt-Jakob disease with cerebellar ataxia at onset in the UKS A Cooper, K L Murray, C A Heath, et al.
Neuroscience Letters|May 2, 2002
14-3-3 in the cerebrospinal fluid of patients with variant and sporadic Creutzfeldt-Jakob disease measured using capture assay able to detect low levels of 14-3-3 proteinAlison J E Green, Sanja Ramljak, Werner E G Müller, et al.
Pageof 5