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Neurology
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June 30, 2006
ALS phenotypes with mutations in CHMP2B (charged multivesicular body protein 2B)
N Parkinson, P G Ince, M O Smith, et al.
Neurology
|
August 22, 2007
Inherited prion disease with 5-OPRI: phenotype modification by repeat length and codon 129
S Mead, T E F Webb, T A Campbell, et al.
Neurology
|
November 27, 2002
Chromosome 3 linked frontotemporal dementia (FTD-3)
S Gydesen, J M Brown, A Brun, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
February 11, 2009
Crystal structure of human prion protein bound to a therapeutic antibody
S V Antonyuk, C R Trevitt, R W Strange, et al.
Lancet (London, England)
|
January 29, 1999
Investigation of variant Creutzfeldt-Jakob disease and other human prion diseases with tonsil biopsy samples
A F Hill, R J Butterworth, S Joiner, et al.
Dementia and Geriatric Cognitive Disorders
|
August 7, 1999
Molecular genetic characterisation of frontotemporal dementia on chromosome 3
A Ashworth, S Lloyd, J Brown, et al.
Der Pathologe
|
March 1, 1996
[Consensus report: tissue handling in suspected Creutzfeldt-Jakob disease and other spongiform encephalopathies (prion diseases) in the human. European Union Biomed-1 Concerted Action]
H Budka, A Aguzzi, P Brown, et al.
Brain : a Journal of Neurology
|
September 2, 2008
Phenotypic heterogeneity and genetic modification of P102L inherited prion disease in an international series
T E F Webb, M Poulter, J Beck, et al.
Molecular Psychiatry
|
October 4, 2018
Predictors for a dementia gene mutation based on gene-panel next-generation sequencing of a large dementia referral series
C Koriath, J Kenny, G Adamson, et al.
Blood Advances
|
July 17, 2025
High-grade B-cell lymphoma, not otherwise specified: an LLMPP study
Brett J Collinge, Laura K Hilton, Jasper Chun Hei Wong, et al.
Page
of 18
Search research articles
Search
Showing results (161-170 of 171) with videos related to
Sort By:
Page
of 18
Neurology
|
June 30, 2006
ALS phenotypes with mutations in CHMP2B (charged multivesicular body protein 2B)
N Parkinson, P G Ince, M O Smith, et al.
Neurology
|
August 22, 2007
Inherited prion disease with 5-OPRI: phenotype modification by repeat length and codon 129
S Mead, T E F Webb, T A Campbell, et al.
Neurology
|
November 27, 2002
Chromosome 3 linked frontotemporal dementia (FTD-3)
S Gydesen, J M Brown, A Brun, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
February 11, 2009
Crystal structure of human prion protein bound to a therapeutic antibody
S V Antonyuk, C R Trevitt, R W Strange, et al.
Lancet (London, England)
|
January 29, 1999
Investigation of variant Creutzfeldt-Jakob disease and other human prion diseases with tonsil biopsy samples
A F Hill, R J Butterworth, S Joiner, et al.
Dementia and Geriatric Cognitive Disorders
|
August 7, 1999
Molecular genetic characterisation of frontotemporal dementia on chromosome 3
A Ashworth, S Lloyd, J Brown, et al.
Der Pathologe
|
March 1, 1996
[Consensus report: tissue handling in suspected Creutzfeldt-Jakob disease and other spongiform encephalopathies (prion diseases) in the human. European Union Biomed-1 Concerted Action]
H Budka, A Aguzzi, P Brown, et al.
Brain : a Journal of Neurology
|
September 2, 2008
Phenotypic heterogeneity and genetic modification of P102L inherited prion disease in an international series
T E F Webb, M Poulter, J Beck, et al.
Molecular Psychiatry
|
October 4, 2018
Predictors for a dementia gene mutation based on gene-panel next-generation sequencing of a large dementia referral series
C Koriath, J Kenny, G Adamson, et al.
Blood Advances
|
July 17, 2025
High-grade B-cell lymphoma, not otherwise specified: an LLMPP study
Brett J Collinge, Laura K Hilton, Jasper Chun Hei Wong, et al.
Page
of 18