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R G Will

Showing results (71-80 of 139) with videos related to

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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.
Nederlands Tijdschrift Voor Geneeskunde|June 1, 1996
[A patient with Creutzfeldt-Jakob disease following treatment with human growth hormone]R A Roos, A R Wintzen, R G Will, et al.
Vox Sanguinis|June 12, 2014
Variant CJD and blood transfusion: are there additional cases?L R R Davidson, C A Llewelyn, J M Mackenzie, et al.
Acta Neurologica Scandinavica|April 14, 2016
Isolated language impairment as the primary presentation of sporadic Creutzfeldt Jakob DiseaseS El Tawil, G Chohan, J Mackenzie, et al.
Neuropathology and Applied Neurobiology|October 29, 2000
Clinicopathological phenotype of codon 129 valine homozygote sporadic Creutzfeldt-Jakob diseaseG G Kovacs, M W Head, T Bunn, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|September 1, 1988
Creutzfeldt-Jakob disease in England and Wales, 1980-1984: a case-control study of potential risk factorsR Harries-Jones, R Knight, R G Will, et al.
British Dental Journal|February 15, 2007
Dental treatment and risk of variant CJD--a case control studyD Everington, A J Smith, H J T Ward, et al.
Vox Sanguinis|December 29, 2015
Creutzfeldt-Jakob disease and blood transfusion: updated results of the UK Transfusion Medicine Epidemiology Review StudyP J M Urwin, J M Mackenzie, C A Llewelyn, et al.
Neurology|March 1, 1996
A prion disease with a novel 96-base pair insertional mutation in the prion protein geneT A Campbell, M S Palmer, R G Will, et al.
Pageof 14

Showing results (71-80 of 139) with videos related to

Sort By:
Pageof 14
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.
Nederlands Tijdschrift Voor Geneeskunde|June 1, 1996
[A patient with Creutzfeldt-Jakob disease following treatment with human growth hormone]R A Roos, A R Wintzen, R G Will, et al.
Vox Sanguinis|June 12, 2014
Variant CJD and blood transfusion: are there additional cases?L R R Davidson, C A Llewelyn, J M Mackenzie, et al.
Acta Neurologica Scandinavica|April 14, 2016
Isolated language impairment as the primary presentation of sporadic Creutzfeldt Jakob DiseaseS El Tawil, G Chohan, J Mackenzie, et al.
Neuropathology and Applied Neurobiology|October 29, 2000
Clinicopathological phenotype of codon 129 valine homozygote sporadic Creutzfeldt-Jakob diseaseG G Kovacs, M W Head, T Bunn, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|September 1, 1988
Creutzfeldt-Jakob disease in England and Wales, 1980-1984: a case-control study of potential risk factorsR Harries-Jones, R Knight, R G Will, et al.
British Dental Journal|February 15, 2007
Dental treatment and risk of variant CJD--a case control studyD Everington, A J Smith, H J T Ward, et al.
Vox Sanguinis|December 29, 2015
Creutzfeldt-Jakob disease and blood transfusion: updated results of the UK Transfusion Medicine Epidemiology Review StudyP J M Urwin, J M Mackenzie, C A Llewelyn, et al.
Neurology|March 1, 1996
A prion disease with a novel 96-base pair insertional mutation in the prion protein geneT A Campbell, M S Palmer, R G Will, et al.
Pageof 14