Related references
Note: Only part of the references are listed.Diagnostic Accuracy of a Combined Analysis of Cerebrospinal Fluid t-PrP, t-tau, p-tau, and Aβ42 in the Differential Diagnosis of Creutzfeldt-Jakob Disease from Alzheimer's Disease with Emphasis on Atypical Disease Variants
Samir Abu Rumeileh et al.
JOURNAL OF ALZHEIMERS DISEASE (2017)
Multiple variants in families with amyotrophic lateral sclerosis and frontotemporal dementia related to C9orf72 repeat expansion: further observations on their oligogenic nature
Maria Pia Giannoccaro et al.
JOURNAL OF NEUROLOGY (2017)
Towards an early clinical diagnosis of sporadic CJD VV2 (ataxic type)
Simone Baiardi et al.
JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY (2017)
Clinical Diagnosis of Progressive Supranuclear Palsy: The Movement Disorder Society Criteria
Guenter U. Hoeglinger et al.
MOVEMENT DISORDERS (2017)
Structural variation in amyloid-β fibrils from Alzheimer's disease clinical subtypes
Wei Qiang et al.
NATURE (2017)
Diagnostic accuracy of CSF neurofilament light chain protein in the biomarker-guided classification system for Alzheimer's disease
Simone Lista et al.
NEUROCHEMISTRY INTERNATIONAL (2017)
Diagnosis and management of dementia with Lewy bodies Fourth consensus report of the DLB Consortium
Ian G. McKeith et al.
NEUROLOGY (2017)
Association of Plasma Neurofilament Light With Neurodegeneration in Patients With Alzheimer Disease
Niklas Mattsson et al.
JAMA NEUROLOGY (2017)
Expansion of the classification of FTLD-TDP: distinct pathology associated with rapidly progressive frontotemporal degeneration
Edward B. Lee et al.
ACTA NEUROPATHOLOGICA (2017)
Evaluation of α-synuclein as a novel cerebrospinal fluid biomarker in different forms of prion diseases
Franc Llorens et al.
ALZHEIMERS & DEMENTIA (2017)
Proteomic differences in amyloid plaques in rapidly progressive and sporadic Alzheimer's disease
Eleanor Drummond et al.
ACTA NEUROPATHOLOGICA (2017)
Prion-specific and surrogate CSF biomarkers in Creutzfeldt-Jakob disease: diagnostic accuracy in relation to molecular subtypes and analysis of neuropathological correlates of p-tau and Aβ42 levels
Francesca Lattanzio et al.
ACTA NEUROPATHOLOGICA (2017)
Comparative analysis of cerebrospinal fluid biomarkers in the differential diagnosis of neurodegenerative dementia
Franc Llorens et al.
ALZHEIMERS & DEMENTIA (2016)
Cerebrospinal fluid markers in the differentiation of molecular subtypes of sporadic Creutzfeldt-Jakob disease
K. Gmitterova et al.
EUROPEAN JOURNAL OF NEUROLOGY (2016)
Neurofilament Light: A Dynamic Cross-Disease Fluid Biomarker for Neurodegeneration
Henrik Zetterberg
NEURON (2016)
Association of Cerebrospinal Fluid Neurofilament Light Concentration With Alzheimer Disease Progression
Henrik Zetterberg et al.
JAMA NEUROLOGY (2016)
Neurofilament light chain: a biomarker for genetic frontotemporal dementia
Lieke H. Meeter et al.
ANNALS OF CLINICAL AND TRANSLATIONAL NEUROLOGY (2016)
Neurofilaments in blood and CSF for diagnosis and prediction of onset in Creutzfeldt-Jakob disease
Petra Steinacker et al.
SCIENTIFIC REPORTS (2016)
Neurofilament subunits are integral components of synapses and modulate neurotransmission and behavior in vivo
A. Yuan et al.
MOLECULAR PSYCHIATRY (2015)
Association of Cerebrospinal Fluid Prion Protein Levels and the Distinction Between Alzheimer Disease and Creutzfeldt-Jakob Disease
Aline Dorey et al.
JAMA NEUROLOGY (2015)
Levels and Age Dependency of Neurofilament Light and Glial Fibrillary Acidic Protein in Healthy Individuals and Their Relation to the Brain Parenchymal Fraction
Mattias Vagberg et al.
PLOS ONE (2015)
Cerebrospinal Fluid Neurofilament Concentration Reflects Disease Severity in Frontotemporal Degeneration
Carole S. Scherling et al.
ANNALS OF NEUROLOGY (2014)
The impact of pre-analytical variables on the stability of neurofilament proteins in CSF, determined by a novel validated SinglePlex Luminex assay and ELISA
Marleen J. A. Koel-Simmelink et al.
JOURNAL OF IMMUNOLOGICAL METHODS (2014)
Validation of next-generation sequencing technologies in genetic diagnosis of dementia
John Beck et al.
NEUROBIOLOGY OF AGING (2014)
CSF neurofilament light differs in neurodegenerative diseases and predicts severity and survival
Tobias Skillback et al.
NEUROLOGY (2014)
Diagnostic Performance of Cerebrospinal Fluid Total Tau and Phosphorylated Tau in Creutzfeldt-Jakob Disease Results From the Swedish Mortality Registry
Tobias Skillback et al.
JAMA NEUROLOGY (2014)
Cerebrospinal fluid neurofilament light chain protein levels in subtypes of frontotemporal dementia
Maria Landqvist Waldo et al.
BMC NEUROLOGY (2013)
Criteria for the diagnosis of corticobasal degeneration
Melissa J. Armstrong et al.
NEUROLOGY (2013)
National Institute on Aging-Alzheimer's Association guidelines for the neuropathologic assessment of Alzheimer's disease: a practical approach
Thomas J. Montine et al.
ACTA NEUROPATHOLOGICA (2012)
Consensus classification of human prion disease histotypes allows reliable identification of molecular subtypes: an inter-rater study among surveillance centres in Europe and USA
Piero Parchi et al.
ACTA NEUROPATHOLOGICA (2012)
Accuracy of a Panel of 5 Cerebrospinal Fluid Biomarkers in the Differential Diagnosis of Patients With Dementia and/or Parkinsonian Disorders
Sara Hall et al.
ARCHIVES OF NEUROLOGY (2012)
Clinical Overlap between Jakob-Creutzfeldt Disease and Lewy Body Disease
Maria Carmela Tartaglia et al.
CANADIAN JOURNAL OF NEUROLOGICAL SCIENCES (2012)
The diagnosis of dementia due to Alzheimer's disease: Recommendations from the National Institute on Aging-Alzheimer's Association workgroups on diagnostic guidelines for Alzheimer's disease
Guy M. McKhann et al.
ALZHEIMERS & DEMENTIA (2011)
Treatable Neurological Disorders Misdiagnosed as Creutzfeldt-Jakob Disease
Numthip Chitravas et al.
ANNALS OF NEUROLOGY (2011)
Sensitivity of revised diagnostic criteria for the behavioural variant of frontotemporal dementia
Katya Rascovsky et al.
BRAIN (2011)
Rapidly Progressive Diffuse Lewy Body Disease
Carles Gaig et al.
MOVEMENT DISORDERS (2011)
Classification of primary progressive aphasia and its variants
M. L. Gorno-Tempini et al.
NEUROLOGY (2011)
Variably Protease-Sensitive Prionopathy: A New Sporadic Disease of the Prion Protein
Wen-Quan Zou et al.
ANNALS OF NEUROLOGY (2010)
CSF Neurofilament Proteins Levels are Elevated in Sporadic Creutzfeldt-Jakob Disease
Jeroen J. J. van Eijk et al.
JOURNAL OF ALZHEIMERS DISEASE (2010)
CSF biomarkers predict a more malignant outcome in Alzheimer disease
A. K. Wallin et al.
NEUROLOGY (2010)
Updated clinical diagnostic criteria for sporadic Creutzfeldt-Jakob disease
I. Zerr et al.
BRAIN (2009)
Inter-Laboratory Assessment of PrPSc Typing in Creutzfeldt-Jakob Disease: A Western Blot Study within the NeuroPrion Consortium
Piero Parchi et al.
BRAIN PATHOLOGY (2009)
Rapidly progressive dementia
Michael D. Geschwind et al.
ANNALS OF NEUROLOGY (2008)
Neurofilament phosphoforms: Surrogate markers for axonal injury, degeneration and loss
A Petzold
JOURNAL OF THE NEUROLOGICAL SCIENCES (2005)
Creutzfeldt-Jakob disease presenting as progressive supranuclear palsy
KA Josephs et al.
EUROPEAN JOURNAL OF NEUROLOGY (2004)
Neurofilament protein in cerebrospinal fluid:: A marker of white matter changes
M Sjögren et al.
JOURNAL OF NEUROSCIENCE RESEARCH (2001)
Share Paper
