Evaluation of α‐synuclein as a novel cerebrospinal fluid biomarker in different forms of prion diseases-Reference-Cited by-同舟云学术

Evaluation of α‐synuclein as a novel cerebrospinal fluid biomarker in different forms of prion diseases

Published:2016-11-18 Issue:6 Volume:13 Page:710-719
ISSN:1552-5260
Container-title:Alzheimer's & Dementia
language:en
Short-container-title:Alzheimer's & Dementia

Author:

Llorens Franc¹²,Kruse Niels³,Schmitz Matthias¹²,Gotzmann Nadine¹²,Golanska Ewa⁴,Thüne Katrin¹²,Zejneli Orgeta⁵,Kanata Eirini⁵,Knipper Tobias¹,Cramm Maria¹²,Lange Peter¹,Zafar Saima¹²,Sikorska Beata⁴,Liberski Pawel P.⁴,Mitrova Eva⁶,Varges Daniela¹,Schmidt Christian¹,Sklaviadis Theodoros⁵,Mollenhauer Brit³⁷⁸,Zerr Inga¹²

Affiliation:

1. Department of Neurology, Clinical Dementia Center University Medical Center Göttingen Göttingen Germany

2. German Center for Neurodegenerative Diseases (DZNE) Site Göttingen Germany

3. Institute for Neuropathology University Medical Center Göttingen Göttingen Germany

4. Department of Molecular Pathology and Neuropathology Medical University of Lodz Lodz Poland

5. Laboratory of Pharmacology, School of Health Sciences, Department of Pharmacy Aristotle University of Thessaloniki Thessaloniki Greece

6. Department of Prion Diseases Slovak Medical University Bratislava Bratislava Slovakia

7. Paracelsus‐Elena Klinik Center for Parkinsonism and Movement Disorders Kassel Germany

8. Department of Neurosurgery University Medical Center Göttingen Göttingen Germany

Funder

European Commission

Publisher

Wiley

Subject

Psychiatry and Mental health,Cellular and Molecular Neuroscience,Geriatrics and Gerontology,Neurology (clinical),Developmental Neuroscience,Health Policy,Epidemiology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1016/j.jalz.2016.09.013

Reference72 articles.

1. Molecular Mechanisms of Prion Pathogenesis

2. An outline of the neuropathology of transmissible spongiform encephalopathies (prion diseases);Liberski PP;Folia Neuropathol,2004

3. Human Prion Diseases

4. Diagnostic Criteria for Sporadic Creutzfeldt-Jakob Disease

5. Updated clinical diagnostic criteria for sporadic Creutzfeldt-Jakob disease

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