Search research articles
Contact Us
Filters
Showing results (131-140 of 138) with videos related to
Page
of 14
Sort By:
You have reached the last page of results.
This site can display upto 138 results.
Journal of Neuropathology and Experimental Neurology
|
June 22, 1999
Frontotemporal dementia and corticobasal degeneration in a family with a P301S mutation in tau
O Bugiani, J R Murrell, G Giaccone, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
January 23, 1996
Vascular variant of prion protein cerebral amyloidosis with tau-positive neurofibrillary tangles: the phenotype of the stop codon 145 mutation in PRNP
B Ghetti, P Piccardo, M G Spillantini, et al.
The American Journal of Pathology
|
June 8, 2001
Prion proteins with different conformations accumulate in Gerstmann-Sträussler-Scheinker disease caused by A117V and F198S mutations
P Piccardo, J J Liepnieks, A William, et al.
Journal of Neural Transmission (Vienna, Austria : 1996)
|
February 24, 2007
Clinical and genetic features of families with frontotemporal dementia and parkinsonism linked to chromosome 17 with a P301S tau mutation
Y Baba, M C Baker, I Le Ber, 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.
Science (New York, N.Y.)
|
May 16, 1997
Effectiveness of anthracycline against experimental prion disease in Syrian hamsters
F Tagliavini, R A McArthur, B Canciani, et al.
Journal of Neuropathology and Experimental Neurology
|
October 24, 1998
Phenotypic variability of Gerstmann-Sträussler-Scheinker disease is associated with prion protein heterogeneity
P Piccardo, S R Dlouhy, P M Lievens, et al.
Neurology
|
February 19, 2010
Worldwide distribution of PSEN1 Met146Leu mutation: a large variability for a founder mutation
A C Bruni, L Bernardi, R Colao, et al.
Page
of 14
Search research articles
Search
Showing results (131-140 of 138) with videos related to
Sort By:
Page
of 14
You have reached the last page of results.
This site can display upto 138 results.
Journal of Neuropathology and Experimental Neurology
|
June 22, 1999
Frontotemporal dementia and corticobasal degeneration in a family with a P301S mutation in tau
O Bugiani, J R Murrell, G Giaccone, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
January 23, 1996
Vascular variant of prion protein cerebral amyloidosis with tau-positive neurofibrillary tangles: the phenotype of the stop codon 145 mutation in PRNP
B Ghetti, P Piccardo, M G Spillantini, et al.
The American Journal of Pathology
|
June 8, 2001
Prion proteins with different conformations accumulate in Gerstmann-Sträussler-Scheinker disease caused by A117V and F198S mutations
P Piccardo, J J Liepnieks, A William, et al.
Journal of Neural Transmission (Vienna, Austria : 1996)
|
February 24, 2007
Clinical and genetic features of families with frontotemporal dementia and parkinsonism linked to chromosome 17 with a P301S tau mutation
Y Baba, M C Baker, I Le Ber, 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.
Science (New York, N.Y.)
|
May 16, 1997
Effectiveness of anthracycline against experimental prion disease in Syrian hamsters
F Tagliavini, R A McArthur, B Canciani, et al.
Journal of Neuropathology and Experimental Neurology
|
October 24, 1998
Phenotypic variability of Gerstmann-Sträussler-Scheinker disease is associated with prion protein heterogeneity
P Piccardo, S R Dlouhy, P M Lievens, et al.
Neurology
|
February 19, 2010
Worldwide distribution of PSEN1 Met146Leu mutation: a large variability for a founder mutation
A C Bruni, L Bernardi, R Colao, et al.
Page
of 14