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M W Head

Showing results (41-50 of 45) with videos related to

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Journal of Clinical Pathology|March 3, 2004
Specificity of lymphoreticular accumulation of prion protein for variant Creutzfeldt-Jakob diseaseD A Hilton, J Sutak, M E F Smith, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|January 15, 2010
Variant CJD infection in the spleen of a neurologically asymptomatic UK adult patient with haemophiliaA Peden, L McCardle, M W Head, et al.
The Lancet. Neurology|April 25, 2006
Predicting susceptibility and incubation time of human-to-human transmission of vCJDM T Bishop, P Hart, L Aitchison, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 30, 2000
Genetic influence on the structural variations of the abnormal prion proteinP Parchi, W Zou, W Wang, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|April 22, 2006
Dura mater-associated Creutzfeldt-Jakob disease: experience from surveillance in the UKC A Heath, R A Barker, T F G Esmonde, et al.
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Showing results (41-50 of 45) with videos related to

Sort By:
Pageof 5
You have reached the last page of results.This site can display upto 45 results.
Journal of Clinical Pathology|March 3, 2004
Specificity of lymphoreticular accumulation of prion protein for variant Creutzfeldt-Jakob diseaseD A Hilton, J Sutak, M E F Smith, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|January 15, 2010
Variant CJD infection in the spleen of a neurologically asymptomatic UK adult patient with haemophiliaA Peden, L McCardle, M W Head, et al.
The Lancet. Neurology|April 25, 2006
Predicting susceptibility and incubation time of human-to-human transmission of vCJDM T Bishop, P Hart, L Aitchison, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 30, 2000
Genetic influence on the structural variations of the abnormal prion proteinP Parchi, W Zou, W Wang, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|April 22, 2006
Dura mater-associated Creutzfeldt-Jakob disease: experience from surveillance in the UKC A Heath, R A Barker, T F G Esmonde, et al.
Pageof 5