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Neuroscience
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June 16, 2010
Cellular prion protein overexpression disturbs cellular homeostasis in SH-SY5Y neuroblastoma cells but does not alter p53 expression: a proteomic study
E Weiss, S Ramljak, A R Asif, et al.
Journal of Neurology
|
November 14, 1997
S-100 protein concentration in the cerebrospinal fluid of patients with Creutzfeldt-Jakob disease
M Otto, H Stein, A Szudra, et al.
Neurology
|
August 28, 2002
Sporadic Creutzfeldt-Jakob disease and surgery: a case-control study using community controls
H J T Ward, D Everington, E A Croes, et al.
Archives of Neurology
|
January 29, 1999
The Heidenhain variant of Creutzfeldt-Jakob disease
S Kropp, W J Schulz-Schaeffer, M Finkenstaedt, et al.
Human Genetics
|
September 15, 2000
Molecular genetics of human prion diseases in Germany
O Windl, A Giese, W Schulz-Schaeffer, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
November 20, 2013
A proposal of new diagnostic pathway for fatal familial insomnia
A Krasnianski, P Sanchez Juan, Claudia Ponto, et al.
Neurology
|
November 18, 1998
Phenotypic variability in fatal familial insomnia (D178N-129M) genotype
I Zerr, A Giese, O Windl, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
June 20, 2001
Patients with Alzheimer's disease and dementia with Lewy bodies mistaken for Creutzfeldt-Jakob disease
H J Tschampa, M Neumann, I Zerr, et al.
Neurology
|
August 19, 2004
Sporadic Creutzfeldt-Jakob disease: magnetic resonance imaging and clinical findings
B Meissner, K Körtner, M Bartl, et al.
Lancet (London, England)
|
May 21, 1999
Codon 129 prion protein genotype and sporadic Creutzfeldt-Jakob disease
A Alperovitch, I Zerr, M Pocchiari, et al.
Page
of 9
Search research articles
Search
Showing results (51-60 of 88) with videos related to
Sort By:
Page
of 9
Neuroscience
|
June 16, 2010
Cellular prion protein overexpression disturbs cellular homeostasis in SH-SY5Y neuroblastoma cells but does not alter p53 expression: a proteomic study
E Weiss, S Ramljak, A R Asif, et al.
Journal of Neurology
|
November 14, 1997
S-100 protein concentration in the cerebrospinal fluid of patients with Creutzfeldt-Jakob disease
M Otto, H Stein, A Szudra, et al.
Neurology
|
August 28, 2002
Sporadic Creutzfeldt-Jakob disease and surgery: a case-control study using community controls
H J T Ward, D Everington, E A Croes, et al.
Archives of Neurology
|
January 29, 1999
The Heidenhain variant of Creutzfeldt-Jakob disease
S Kropp, W J Schulz-Schaeffer, M Finkenstaedt, et al.
Human Genetics
|
September 15, 2000
Molecular genetics of human prion diseases in Germany
O Windl, A Giese, W Schulz-Schaeffer, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
November 20, 2013
A proposal of new diagnostic pathway for fatal familial insomnia
A Krasnianski, P Sanchez Juan, Claudia Ponto, et al.
Neurology
|
November 18, 1998
Phenotypic variability in fatal familial insomnia (D178N-129M) genotype
I Zerr, A Giese, O Windl, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
June 20, 2001
Patients with Alzheimer's disease and dementia with Lewy bodies mistaken for Creutzfeldt-Jakob disease
H J Tschampa, M Neumann, I Zerr, et al.
Neurology
|
August 19, 2004
Sporadic Creutzfeldt-Jakob disease: magnetic resonance imaging and clinical findings
B Meissner, K Körtner, M Bartl, et al.
Lancet (London, England)
|
May 21, 1999
Codon 129 prion protein genotype and sporadic Creutzfeldt-Jakob disease
A Alperovitch, I Zerr, M Pocchiari, et al.
Page
of 9