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Cerebrospinal fluid amyloid beta and tau proteins in atypical Parkinsonism: a review
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作者 Vasilios C.Constantinides George P.Paraskevas +4 位作者 Fotini Boufidou mara bourbouli Panagiotis G.Paraskevas Leonidas Stefanis Elisabeth Kapaki 《Neuroimmunology and Neuroinflammation》 2020年第2期120-131,共12页
Progressive supranuclear palsy,corticobasal degeneration,multiple system atrophy and dementia with Lewy bodies are the most common causes of atypical Parkinsonism and enter the differential diagnosis of Parkinson'... Progressive supranuclear palsy,corticobasal degeneration,multiple system atrophy and dementia with Lewy bodies are the most common causes of atypical Parkinsonism and enter the differential diagnosis of Parkinson's disease.multiple system atrophy,dementia with Lewy bodies and Parkinson's disease are synucleinopathies,whereas progressive supranuclear palsy and corticobasal degeneration are tauopathies.Multiple cerebrospinal fluid markers have been applied on cohorts of patients with Parkinsonism,with the aim to develop biomarkers for these disorders.Total tau(τΤ),phosphorylated tau at threonine 181(τP-181)and amyloid-beta with 42 amino acids(Aβ42)are considered classical biomarkers for Alzheimer's disease.The aim of the present study is to review the literature regarding these classical cerebrospinal fluid biomarkers in cohorts with Parkinsonism,as well as present data on novel approaches regarding analysis of these proteins. 展开更多
关键词 Biomarkers cerebrospinal fluid progressive supranuclear palsy corticobasal degeneration multiple system atrophy dementia with Lewy bodies tau protein phosphorylated tau protein amyloid beta
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The emerging TDP-43 proteinopathy
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作者 George P.Paraskevas mara bourbouli +1 位作者 Ioannis Zaganas Elisabeth Kapaki 《Neuroimmunology and Neuroinflammation》 2018年第5期4-6,共3页
Currently, neurodegenerative diseases are viewed as proteinopathies. In this context, a specific protein or peptide is involved in the pathogenesis of the disease by missfolding, polymerization, reduced degradation an... Currently, neurodegenerative diseases are viewed as proteinopathies. In this context, a specific protein or peptide is involved in the pathogenesis of the disease by missfolding, polymerization, reduced degradation and final accumulation in the form of insoluble inclusions leading to neurodegeneration by various interacting mechanisms[1,2]. 展开更多
关键词 The EMERGING TDP-43 NEURODEGENERATIVE DISEASES
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