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R G Will

Showing results (61-70 of 139) with videos related to

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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.
Transfusion Medicine (Oxford, England)|December 3, 1999
Variant Creutzfeldt-Jakob disease is not related to underlying IgA deficiencyG R Barclay, R Munks, G E Stewart, et al.
Neurology|April 11, 2001
Misleading results with the 14-3-3 assay for the diagnosis of Creutzfeldt-Jakob diseaseA J Green, R S Knight, M A Macleod, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|May 18, 2004
Is variant Creutzfeldt-Jakob disease in young children misdiagnosed as Alpers' syndrome? An analysis of a national surveillance studyJ te Water Naudé, C M Verity, R G Will, et al.
Archives of Disease in Childhood|January 8, 2004
Variations in neurodegenerative disease across the UK: findings from the national study of Progressive Intellectual and Neurological Deterioration (PIND)G Devereux, L Stellitano, C M Verity, et al.
Histopathology|August 10, 2000
Laboratory diagnosis of variant Creutzfeldt-Jakob diseaseJ W Ironside, M W Head, J E Bell, et al.
Lancet (London, England)|October 5, 1996
Cerebrospinal-fluid test for new-variant Creutzfeldt-Jakob diseaseR G Will, M Zeidler, P Brown, et al.
Brain Pathology (Zurich, Switzerland)|July 21, 1998
FFI cases from the United KingdomR G Will, M J Campbell, T H Moss, et al.
BMJ (Clinical Research Ed.)|July 31, 1998
New variant Creutzfeldt-Jakob disease is more common in Britain than elsewhereJ W Ironside, R S Knight, R G Will, et al.
Clinical Radiology|October 5, 2001
MRI of Creutzfeldt-Jakob disease: imaging features and recommended MRI protocolD A Collie, R J Sellar, M Zeidler, et al.
Pageof 14

Showing results (61-70 of 139) with videos related to

Sort By:
Pageof 14
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.
Transfusion Medicine (Oxford, England)|December 3, 1999
Variant Creutzfeldt-Jakob disease is not related to underlying IgA deficiencyG R Barclay, R Munks, G E Stewart, et al.
Neurology|April 11, 2001
Misleading results with the 14-3-3 assay for the diagnosis of Creutzfeldt-Jakob diseaseA J Green, R S Knight, M A Macleod, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|May 18, 2004
Is variant Creutzfeldt-Jakob disease in young children misdiagnosed as Alpers' syndrome? An analysis of a national surveillance studyJ te Water Naudé, C M Verity, R G Will, et al.
Archives of Disease in Childhood|January 8, 2004
Variations in neurodegenerative disease across the UK: findings from the national study of Progressive Intellectual and Neurological Deterioration (PIND)G Devereux, L Stellitano, C M Verity, et al.
Histopathology|August 10, 2000
Laboratory diagnosis of variant Creutzfeldt-Jakob diseaseJ W Ironside, M W Head, J E Bell, et al.
Lancet (London, England)|October 5, 1996
Cerebrospinal-fluid test for new-variant Creutzfeldt-Jakob diseaseR G Will, M Zeidler, P Brown, et al.
Brain Pathology (Zurich, Switzerland)|July 21, 1998
FFI cases from the United KingdomR G Will, M J Campbell, T H Moss, et al.
BMJ (Clinical Research Ed.)|July 31, 1998
New variant Creutzfeldt-Jakob disease is more common in Britain than elsewhereJ W Ironside, R S Knight, R G Will, et al.
Clinical Radiology|October 5, 2001
MRI of Creutzfeldt-Jakob disease: imaging features and recommended MRI protocolD A Collie, R J Sellar, M Zeidler, et al.
Pageof 14