Results 51 to 60 of about 26,898 (212)

Tau protein, A beta 42 and S-100B protein in cerebrospinal fluid of patients with dementia with Lewy bodies [PDF]

, 2005
The intra vitam diagnosis of dementia with Lewy bodies (DLB) is still based on clinical grounds. So far no technical investigations have been available to support this diagnosis.
Arai H, Barbara Ciesielczyk, Brit Mollenhauer, Claudia Trenkwalder, Galasko D, Hans A. Kretzschmar, Hansen LA, Hulstaert F, Jens Wiltfang, Kanemaru K, Lukas Cepek, Manuela Neumann, Markus Otto, McKeith I, McKeith IG, McKhann G, Merdes AR, Mirko Bibl, Molina L, Otto M, Parnetti L, Petra Steinacker, Sigrid Poser, Tschampa HJ, Walter J. Schulz-Schaeffer, Watson GS   +25 more
core   +1 more source

The Importance of Rapid Consideration of Creutzfeldt- Jakob Disease in the Differential Diagnosis of Progressive Neurodegenerative Disease: A Case Report

International Journal of Medical Students, 2016
Background: Creutzfeldt-Jakob disease (CJD) is a prion disease characterized by misfolded proteins that lead to neurodegeneration and inevitable death. Classic sporadic CJD presents primarily with cognitive symptoms and ataxia without visual impairment ...
Arthur Joseph, Jacob Core, Daniel Solano, Marquand Patton, Shaun Smart   +4 more
doaj   +1 more source

Revisiting protein aggregation as pathogenic in sporadic Parkinson and Alzheimer diseases. [PDF]

, 2019
The gold standard for a definitive diagnosis of Parkinson disease (PD) is the pathologic finding of aggregated α-synuclein into Lewy bodies and for Alzheimer disease (AD) aggregated amyloid into plaques and hyperphosphorylated tau into tangles.
Brundin, P, Cambi, F, Espay, AJ, Fasano, A, Fernandez, HH, Gan-Or, Z, Greenamyre, JT, Josephs, KA, Kauffman, MA, Lang, AE, Leverenz, JB, Litvan, I, Marsili, L, Mata, IF, Merola, A, Morgante, F, Perry, G, Sardi, SP, Savica, R, Schwarzschild, MA, Sherer, T, Simon, DK, Standaert, DG, Tanner, CM, Vizcarra, JA, Yamasaki, TR, Zabetian, CP   +26 more
core   +3 more sources

Creutzfeldt-Jakob disease and sleep disorders

Chinese Journal of Contemporary Neurology and Neurosurgery, 2018
Creutzfeldt-Jakob disease (CJD) is a fatal neurodegenerative disease caused by prion protein infection. Compared with other neurodegenerative diseases, neuronal cell apoptosis in CJD occurs more rapidly.
Jian-nan ZHU, Li CUI, Qing-qing SUN, Qian-qian CHEN, Ya-nan ZHANG, Zan WANG   +5 more
doaj   +1 more source

Functional Magnetic Resonance Imaging in the Final Stage of Creutzfeldt-Jakob Disease

Diagnostics, 2020
Sporadic Creutzfeldt-Jakob disease (sCJD) is a rare fatal degenerative disease of the central nervous system. The clinical course is characterized by rapid progression of neurological and neuromuscular symptoms.
Stefan M. Golaszewski, Bettina Wutzl, Axel F. Unterrainer, Cristina Florea, Kerstin Schwenker, Vanessa N. Frey, Martin Kronbichler, Frank Rattay, Raffaele Nardone, Larissa Hauer, Johann Sellner, Eugen Trinka   +11 more
doaj   +1 more source

Health professions and risk of sporadic Creutzfeldt- Jakob disease, 1965 to 2010 [PDF]

, 2012
In 2009, a pathologist with sporadic Creutzfeldt- Jakob Disease (sCJD) was reported to the Spanish registry. This case prompted a request for information on health-related occupation in sCJD cases from countries participating in the European Creutzfeldt ...
Alcalde-Cabero, E., Almazán-Isla, J., Brandel, J-P. (Jean-Philippe), Breithaupt, M., Catarino, J., Collins, S.J. (Steven), Haybäck, J., Höftberger, R. (Romana), Kahana, E., Kovacs, G.G. (Gabor), Ladogana, A. (Anna), Mitrová, E. (Eva), Molesworth, A., Nakamura, Y., Pedro-Cuesta, J. (Jesús) de, Pocchiari, M. (Maurizio), Popovic, M., Ruiz-Tovar, M., Taratuto, A., van Duin, C., Will, R.G. (Robert), Yamada, M., Zerr, I. (Inga)   +22 more
core   +2 more sources

Intra- and interspecies interactions between prion proteins and effects of mutations and polymorphisms [PDF]

, 2003
Recently, crystallization of the prion protein in a dimeric form was reported. Here we show that native soluble homogenous FLAG-tagged prion proteins from hamster, man and cattle expressed in the baculovirus system are predominantly dimeric.
Bradley R., Campbell T.A., Clark W.W., Cutlip R.C., Edenhofer F., Goldfarb L.G., Krasemann S., Leucht C., Lopez L., Majtenyi C., Scott M.R., Weiss S.   +11 more
core   +1 more source

Patterns of Postictal Abnormalities in Relation to Status Epilepticus in Adults

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective Abnormalities on peri‐ictal diffusion‐weighted magnetic resonance imaging (DWI‐PMAs) are well‐established for patients with status epilepticus (SE), but knowledge on patterns of DWI‐PMAs and their prognostic impact is sparse. Methods This systematic review and individual participant data meta‐analysis included observational studies ...
Andrea Enerstad Bolle, Silvana Sarria‐Estrada, Thomas Bonduelle, Bertram Daniel Dynesen, Manuel Toledo, Zhu Chung Che, Kjell Heuser, Anastasios Chatzikonstantinou, Jérôme Aupy, Udaya Seneviratne, Estevo Santamarina Perez, Christoph Patrick Beier   +11 more
wiley   +1 more source

ZNRD2 Mediated Nucleoprotein Aggregation Impairs Respiratory Syncytial Virus Replication

Advanced Science, EarlyView.
During RSV infection, nucleoprotein (N) forms RNA‐bound oligomers. The host protein ZNRD2 binds to these oligomers, promoting their transition into insoluble aggregates. These aggregates simultaneously sequester functional N to restrict viral production and disrupt chaperonin assembly quality control by interfering with ZNRD2's role as an adaptor ...
Haiwu Zhou, Mingbin He, Jinhong Du, Cong Liu, Weiwei Wang, Yuewen Han, Zhifei Li, Yali Qin, Mingzhou Chen   +8 more
wiley   +1 more source

Atypical status of bovine spongiform encephalopathy in Poland: a molecular typing study [PDF]

, 2008
The aim of this study was to analyze molecular features of protease-resistant prion protein (PrPres) in Western blots of BSE cases diagnosed in Poland with respect to a possible atypical status.
Jacobs, J.G., Langeveld, J.P.M., Polak, M.P., Zmudzinski, J.F.   +3 more
core   +1 more source