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Neurology
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April 23, 2008
A novel PSEN2 mutation associated with a peculiar phenotype
P Piscopo, G Marcon, M R Piras, et al.
Journal of Chromatography. A
|
July 15, 2005
Identification of the pathological prion protein allotypes in scrapie-infected heterozygous bank voles (Clethrionomys glareolus) by high-performance liquid chromatography-mass spectrometry
C Cartoni, M E Schininà, B Maras, et al.
Neurology
|
November 9, 2000
Iatrogenic Creutzfeldt-Jakob disease at the millennium
P Brown, M Preece, J P Brandel, et al.
European Journal of Neurology
|
January 26, 2008
Codon 129 polymorphism of prion protein gene in sporadic Alzheimer's disease
A Poleggi, A Bizzarro, A Acciarri, et al.
American Journal of Human Genetics
|
March 26, 1999
Ancestral origins and worldwide distribution of the PRNP 200K mutation causing familial Creutzfeldt-Jakob disease
H S Lee, N Sambuughin, L Cervenakova, 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.
Neurology
|
September 20, 2000
Analysis of EEG and CSF 14-3-3 proteins as aids to the diagnosis of Creutzfeldt-Jakob disease
I Zerr, M Pocchiari, S Collins, et al.
Euro Surveillance : Bulletin Europeen Sur Les Maladies Transmissibles = European Communicable Disease Bulletin
|
April 21, 2012
Health professions and risk of sporadic Creutzfeldt-Jakob disease, 1965 to 2010
E Alcalde-Cabero, J Almazan-Isla, J P Brandel, 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.
Brain : a Journal of Neurology
|
September 14, 2004
Predictors of survival in sporadic Creutzfeldt-Jakob disease and other human transmissible spongiform encephalopathies
M Pocchiari, M Puopolo, E A Croes, et al.
Page
of 7
Search research articles
Search
Showing results (51-60 of 63) with videos related to
Sort By:
Page
of 7
Neurology
|
April 23, 2008
A novel PSEN2 mutation associated with a peculiar phenotype
P Piscopo, G Marcon, M R Piras, et al.
Journal of Chromatography. A
|
July 15, 2005
Identification of the pathological prion protein allotypes in scrapie-infected heterozygous bank voles (Clethrionomys glareolus) by high-performance liquid chromatography-mass spectrometry
C Cartoni, M E Schininà, B Maras, et al.
Neurology
|
November 9, 2000
Iatrogenic Creutzfeldt-Jakob disease at the millennium
P Brown, M Preece, J P Brandel, et al.
European Journal of Neurology
|
January 26, 2008
Codon 129 polymorphism of prion protein gene in sporadic Alzheimer's disease
A Poleggi, A Bizzarro, A Acciarri, et al.
American Journal of Human Genetics
|
March 26, 1999
Ancestral origins and worldwide distribution of the PRNP 200K mutation causing familial Creutzfeldt-Jakob disease
H S Lee, N Sambuughin, L Cervenakova, 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.
Neurology
|
September 20, 2000
Analysis of EEG and CSF 14-3-3 proteins as aids to the diagnosis of Creutzfeldt-Jakob disease
I Zerr, M Pocchiari, S Collins, et al.
Euro Surveillance : Bulletin Europeen Sur Les Maladies Transmissibles = European Communicable Disease Bulletin
|
April 21, 2012
Health professions and risk of sporadic Creutzfeldt-Jakob disease, 1965 to 2010
E Alcalde-Cabero, J Almazan-Isla, J P Brandel, 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.
Brain : a Journal of Neurology
|
September 14, 2004
Predictors of survival in sporadic Creutzfeldt-Jakob disease and other human transmissible spongiform encephalopathies
M Pocchiari, M Puopolo, E A Croes, et al.
Page
of 7