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M W Head

Showing results (31-40 of 45) with videos related to

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The American Journal of Pathology|February 18, 1998
Fatal encephalopathy with astrocyte inclusions in GFAP transgenic miceA Messing, M W Head, K Galles, et al.
Neuropathology and Applied Neurobiology|June 4, 2009
Pathological investigation of the first blood donor and recipient pair linked by transfusion-associated variant Creutzfeldt-Jakob disease transmissionM W Head, H M Yull, D L Ritchie, et al.
Neuropathology and Applied Neurobiology|January 22, 2011
RNA integrity in post mortem human variant Creutzfeldt-Jakob disease (vCJD) and control brain tissueK R Sherwood, M W Head, R Walker, 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|December 20, 2005
Raised CSF phospho-tau concentrations in variant Creutzfeldt-Jakob disease: diagnostic and pathological implicationsC A Goodall, M W Head, D Everington, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|June 16, 2010
The first case of protease-sensitive prionopathy (PSPr) in The Netherlands: a patient with an unusual GSS-like clinical phenotypeC Jansen, M W Head, W A van Gool, et al.
Annals of Neurology|August 17, 2001
Sporadic Creutzfeldt-Jakob disease in a young Dutch valine homozygote: atypical molecular phenotypeM W Head, G Tissingh, B M Uitdehaag, et al.
The British Journal of Ophthalmology|August 23, 2005
Abnormal prion protein in the retina of the most commonly occurring subtype of sporadic Creutzfeldt-Jakob diseaseM W Head, A H Peden, H M Yull, et al.
The Journal of Pathology|July 7, 2007
In vitro amplification and detection of variant Creutzfeldt-Jakob disease PrPScM Jones, A H Peden, C V Prowse, et al.
The Journal of Pathology|October 24, 2007
Disease-associated prion protein is not detectable in human systemic amyloid depositsG A Tennent, M W Head, M Bishop, et al.
Pageof 5

Showing results (31-40 of 45) with videos related to

Sort By:
Pageof 5
The American Journal of Pathology|February 18, 1998
Fatal encephalopathy with astrocyte inclusions in GFAP transgenic miceA Messing, M W Head, K Galles, et al.
Neuropathology and Applied Neurobiology|June 4, 2009
Pathological investigation of the first blood donor and recipient pair linked by transfusion-associated variant Creutzfeldt-Jakob disease transmissionM W Head, H M Yull, D L Ritchie, et al.
Neuropathology and Applied Neurobiology|January 22, 2011
RNA integrity in post mortem human variant Creutzfeldt-Jakob disease (vCJD) and control brain tissueK R Sherwood, M W Head, R Walker, 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|December 20, 2005
Raised CSF phospho-tau concentrations in variant Creutzfeldt-Jakob disease: diagnostic and pathological implicationsC A Goodall, M W Head, D Everington, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|June 16, 2010
The first case of protease-sensitive prionopathy (PSPr) in The Netherlands: a patient with an unusual GSS-like clinical phenotypeC Jansen, M W Head, W A van Gool, et al.
Annals of Neurology|August 17, 2001
Sporadic Creutzfeldt-Jakob disease in a young Dutch valine homozygote: atypical molecular phenotypeM W Head, G Tissingh, B M Uitdehaag, et al.
The British Journal of Ophthalmology|August 23, 2005
Abnormal prion protein in the retina of the most commonly occurring subtype of sporadic Creutzfeldt-Jakob diseaseM W Head, A H Peden, H M Yull, et al.
The Journal of Pathology|July 7, 2007
In vitro amplification and detection of variant Creutzfeldt-Jakob disease PrPScM Jones, A H Peden, C V Prowse, et al.
The Journal of Pathology|October 24, 2007
Disease-associated prion protein is not detectable in human systemic amyloid depositsG A Tennent, M W Head, M Bishop, et al.
Pageof 5