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Plasma total prion protein as a potential biomarker for neurodegenerative dementia: diagnostic accuracy in the spectrum of prion diseases

Neuropathology and applied neurobiology, 2020-04, Vol.46 (3), p.240-254

2020

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Interlaboratory validation of cerebrospinal fluid α-synuclein quantification in the diagnosis of sporadic Creutzfeldt-Jakob disease

Alzheimer's & dementia : diagnosis, assessment & disease monitoring, 2018, Vol.10 (1), p.461-470

2018

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CSF neurogranin as a neuronal damage marker in CJD: a comparative study with AD

Journal of neurology, neurosurgery and psychiatry, 2019-08, Vol.90 (8), p.846

2019

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Diagnostic and prognostic value of plasma neurofilament light and total-tau in sporadic Creutzfeldt-Jakob disease

Alzheimer's research & therapy, 2021-04, Vol.13 (1), p.86-86, Article 86

2021

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TREM2 expression in the brain and biological fluids in prion diseases

Acta neuropathologica, 2021-06, Vol.141 (6), p.841-859

2021

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The small GTPase Rab11 co-localizes with -synuclein in intracellular inclusions and modulates its aggregation, secretion and toxicity

Human molecular genetics, 2014-12, Vol.23 (25), p.6732-6745

2014

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Seeding variability of different alpha synuclein strains in synucleinopathies

Annals of neurology, 2019-05, Vol.85 (5), p.691-703

2019

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Validation of Plasma Neurofilament Light Chain as a Marker for α‐Synucleinopathies

Movement disorders, 2021-11, Vol.36 (11), p.2701-2703

2021

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A prognostic model for overall survival in sporadic Creutzfeldt‐Jakob disease

Alzheimer's & dementia, 2020-10, Vol.16 (10), p.1438-1447

2020

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Plasma YKL-40 in the spectrum of neurodegenerative dementia

Journal of neuroinflammation, 2019-07, Vol.16 (1), p.145-145, Article 145

2019

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Cerebrospinal fluid neurogranin as a new player in prion disease diagnosis and prognosis

Neural regeneration research, 2020-05, Vol.15 (5), p.861-862

2020

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The Interplay between Alpha-Synuclein Clearance and Spreading

Biomolecules, 2015-04, Vol.5 (2), p.435-471

2015

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Cerebrospinal fluid non-phosphorylated tau in the differential diagnosis of Creutzfeldt–Jakob disease: a comparative prospective study with 14-3-3

Journal of neurology, 2020-02, Vol.267 (2), p.543-550

2020

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Validation of Plasma and CSF Neurofilament Light Chain as an Early Marker for Sporadic Creutzfeldt-Jakob Disease

Molecular neurobiology, 2022-09, Vol.59 (9), p.1-9

2022

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Detection of Cerebrospinal Fluid Neurofilament Light Chain as a Marker for Alpha-Synucleinopathies

Frontiers in aging neuroscience, 2021-09, Vol.13, p.717930-717930

2021

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Cerebrospinal fluid neurofilament light in suspected sporadic Creutzfeldt-Jakob disease

Journal of clinical neuroscience, 2019-02, Vol.60, p.124-127

2019

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The small GTPase Rab11 co-localizes with α-synuclein in intracellular inclusions and modulates its aggregation, secretion and toxicity

Human molecular genetics, 2014-12, Vol.23 (25), p.6732-6745

2014

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Correction: Comparative evaluation of clinical and cerebrospinal fluid biomarker characteristics in rapidly and non‑rapidly progressive Alzheimer's disease

Alzheimer's research & therapy, 2023-06, Vol.15 (1), p.116-116, Article 116

2023

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Cerebrospinal Fluid Prion Disease Biomarkers in Pre-clinical and Clinical Naturally Occurring Scrapie

Molecular neurobiology, 2018-11, Vol.55 (11), p.8586-8591

2018

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Applications of the real-time quaking-induced conversion assay in diagnosis, prion strain-typing, drug pre-screening and other amyloidopathies

Expert review of molecular diagnostics, 2017-10, Vol.17 (10), p.897-904

2017

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Validation of Poly(Propylene Imine) Glycodendrimers Towards Their Anti-prion Conversion Efficiency

Molecular neurobiology, 2020-04, Vol.57 (4), p.1863-1874

2020

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Amyloid-like protein inclusions in tobacco transgenic plants

PloS one, 2010-10, Vol.5 (10), p.e13625-e13625

2010

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Optimization of the Real-Time Quaking-Induced Conversion Assay for Prion Disease Diagnosis

Frontiers in bioengineering and biotechnology, 2020-11, Vol.8, p.586890-586890

2020

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Yeast prions form infectious amyloid inclusion bodies in bacteria

Microbial cell factories, 2012-06, Vol.11 (1), p.89-89, Article 89

2012

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Structure, function and toxicity of alpha‐synuclein: the Bermuda triangle in synucleinopathies

Journal of neurochemistry, 2016-10, Vol.139 (S1), p.240-255

2016

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Plasma total prion protein as a potential biomarker for neurodegenerative dementia: diagnostic accuracy in the spectrum of prion diseases

Interlaboratory validation of cerebrospinal fluid α-synuclein quantification in the diagnosis of sporadic Creutzfeldt-Jakob disease

CSF neurogranin as a neuronal damage marker in CJD: a comparative study with AD

Diagnostic and prognostic value of plasma neurofilament light and total-tau in sporadic Creutzfeldt-Jakob disease

TREM2 expression in the brain and biological fluids in prion diseases

The small GTPase Rab11 co-localizes with -synuclein in intracellular inclusions and modulates its aggregation, secretion and toxicity

Seeding variability of different alpha synuclein strains in synucleinopathies

Validation of Plasma Neurofilament Light Chain as a Marker for α‐Synucleinopathies

A prognostic model for overall survival in sporadic Creutzfeldt‐Jakob disease

Plasma YKL-40 in the spectrum of neurodegenerative dementia

Cerebrospinal fluid neurogranin as a new player in prion disease diagnosis and prognosis

The Interplay between Alpha-Synuclein Clearance and Spreading

Cerebrospinal fluid non-phosphorylated tau in the differential diagnosis of Creutzfeldt–Jakob disease: a comparative prospective study with 14-3-3

Validation of Plasma and CSF Neurofilament Light Chain as an Early Marker for Sporadic Creutzfeldt-Jakob Disease

Detection of Cerebrospinal Fluid Neurofilament Light Chain as a Marker for Alpha-Synucleinopathies

Cerebrospinal fluid neurofilament light in suspected sporadic Creutzfeldt-Jakob disease

The small GTPase Rab11 co-localizes with α-synuclein in intracellular inclusions and modulates its aggregation, secretion and toxicity

Correction: Comparative evaluation of clinical and cerebrospinal fluid biomarker characteristics in rapidly and non‑rapidly progressive Alzheimer's disease

Cerebrospinal Fluid Prion Disease Biomarkers in Pre-clinical and Clinical Naturally Occurring Scrapie

Applications of the real-time quaking-induced conversion assay in diagnosis, prion strain-typing, drug pre-screening and other amyloidopathies

Validation of Poly(Propylene Imine) Glycodendrimers Towards Their Anti-prion Conversion Efficiency

Amyloid-like protein inclusions in tobacco transgenic plants

Optimization of the Real-Time Quaking-Induced Conversion Assay for Prion Disease Diagnosis

Yeast prions form infectious amyloid inclusion bodies in bacteria

Structure, function and toxicity of alpha‐synuclein: the Bermuda triangle in synucleinopathies

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