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Journal of Neurochemistry
|
February 2, 2018
Elemental fingerprint as a cerebrospinal fluid biomarker for the diagnosis of Parkinson's disease
Fabian Maass, Bernhard Michalke, Andreas Leha, et al.
Journal of Alzheimer'S Disease : JAD
|
June 10, 2017
Neuropsychological Symptoms in Sporadic Creutzfeldt-Jakob Disease Patients in Germany
Anna Krasnianski, Geeske T Bohling, Uta Heinemann, et al.
Dementia and Geriatric Cognitive Disorders
|
March 8, 2013
Report about four novel mutations in the prion protein gene
Gabi Schelzke, Katharina Stoeck, Sabina Eigenbrod, et al.
Brain : a Journal of Neurology
|
February 13, 2014
High molecular mass assemblies of amyloid-β oligomers bind prion protein in patients with Alzheimer's disease
Frank Dohler, Diego Sepulveda-Falla, Susanne Krasemann, et al.
Restorative Neurology and Neuroscience
|
April 24, 2008
Overexpression of cellular prion protein alters postischemic Erk1/2 phosphorylation but not Akt phosphorylation and protects against focal cerebral ischemia
Jens Weise, Thorsten R Doeppner, Tilo Müller, et al.
Cell Death & Disease
|
January 20, 2017
Cellular prion protein mediates early apoptotic proteome alternation and phospho-modification in human neuroblastoma cells
Saima Zafar, Christina Behrens, Hassan Dihazi, et al.
Journal of Neurology
|
June 20, 2003
Diagnostic problems during late course in Creutzfeldt-Jakob disease
Brit Mollenhauer, Siegfried Serafin, Inga Zerr, et al.
Neurobiology of Aging
|
March 10, 2015
Cerebrospinal fluid tau levels are a marker for molecular subtype in sporadic Creutzfeldt-Jakob disease
André Karch, Peter Hermann, Claudia Ponto, et al.
Pathogens (Basel, Switzerland)
|
May 24, 2024
A Comparison of RML Prion Inactivation Efficiency by Heterogeneous and Homogeneous Photocatalysis
Ioannis Paspaltsis, Eirini Kanata, Sotirios Sotiriadis, et al.
Neurobiology of Aging
|
September 11, 2019
A novel V272D presenilin mutation associated with logopenia, disorientation, and apraxia in an autosomal-dominant Alzheimer's disease family
David Mengel, Lei Liu, Raina Yamamoto, et al.
Page
of 36
Search research articles
Search
Showing results (151-160 of 358) with videos related to
Sort By:
Page
of 36
Journal of Neurochemistry
|
February 2, 2018
Elemental fingerprint as a cerebrospinal fluid biomarker for the diagnosis of Parkinson's disease
Fabian Maass, Bernhard Michalke, Andreas Leha, et al.
Journal of Alzheimer'S Disease : JAD
|
June 10, 2017
Neuropsychological Symptoms in Sporadic Creutzfeldt-Jakob Disease Patients in Germany
Anna Krasnianski, Geeske T Bohling, Uta Heinemann, et al.
Dementia and Geriatric Cognitive Disorders
|
March 8, 2013
Report about four novel mutations in the prion protein gene
Gabi Schelzke, Katharina Stoeck, Sabina Eigenbrod, et al.
Brain : a Journal of Neurology
|
February 13, 2014
High molecular mass assemblies of amyloid-β oligomers bind prion protein in patients with Alzheimer's disease
Frank Dohler, Diego Sepulveda-Falla, Susanne Krasemann, et al.
Restorative Neurology and Neuroscience
|
April 24, 2008
Overexpression of cellular prion protein alters postischemic Erk1/2 phosphorylation but not Akt phosphorylation and protects against focal cerebral ischemia
Jens Weise, Thorsten R Doeppner, Tilo Müller, et al.
Cell Death & Disease
|
January 20, 2017
Cellular prion protein mediates early apoptotic proteome alternation and phospho-modification in human neuroblastoma cells
Saima Zafar, Christina Behrens, Hassan Dihazi, et al.
Journal of Neurology
|
June 20, 2003
Diagnostic problems during late course in Creutzfeldt-Jakob disease
Brit Mollenhauer, Siegfried Serafin, Inga Zerr, et al.
Neurobiology of Aging
|
March 10, 2015
Cerebrospinal fluid tau levels are a marker for molecular subtype in sporadic Creutzfeldt-Jakob disease
André Karch, Peter Hermann, Claudia Ponto, et al.
Pathogens (Basel, Switzerland)
|
May 24, 2024
A Comparison of RML Prion Inactivation Efficiency by Heterogeneous and Homogeneous Photocatalysis
Ioannis Paspaltsis, Eirini Kanata, Sotirios Sotiriadis, et al.
Neurobiology of Aging
|
September 11, 2019
A novel V272D presenilin mutation associated with logopenia, disorientation, and apraxia in an autosomal-dominant Alzheimer's disease family
David Mengel, Lei Liu, Raina Yamamoto, et al.
Page
of 36