Results 121 to 130 of about 7,256 (169)

Distinct cerebrospinal fluid proteomic signatures define clinicopathological subtypes of sporadic Creutzfeldt-Jakob disease and predict patient survival. [PDF]

Acta Neuropathol Commun
Bentivenga GM, Mammana A, Gogishvili D, Baiardi S, Vittoriosi E, Mastrangelo A, Ranieri A, Houtkamp IM, Brockmann K, Abeln S, Capellari S, Parchi P.   +11 more
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A critical perspective of prion disease surveillance in Brazil. [PDF]

Front Neurosci
Barbosa BJAP, Montenegro MLV, da Cunha JEG.   +2 more
europepmc   +1 more source

Coexistence of CSF anti-Ma2 antibody and 14-3-3 protein: a diagnostic dilemma between autoimmune encephalitis and Creutzfeldt-Jakob disease, a Case Report. [PDF]

Front Immunol
Sun N, Zou L, Deng J, Wei F, Zhang H.
europepmc   +1 more source

Peripheral Signatures of Multidimensional Pathology in Symptomatic and Asymptomatic Creutzfeldt-Jakob Disease. [PDF]

CNS Neurosci Ther
Chen ZY, Chu M, Wang YH, Liu R, Zhang J, Yue AL, Lu H, He QQ, Hou JH, Chen YF, Ye H, Wu LY.   +11 more
europepmc   +1 more source

[Creutzfeldt-Jakob syndrome. A new variant in Great Britain].

Tidsskrift for den Norske laegeforening : tidsskrift for praktisk medicin, ny raekke, 1996
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Lithium-Induced Creutzfeldt-Jakob Syndrome

Clinical Neuropharmacology, 1996
a 67-year-old man with bipolar disorder developed a Creutzfeldt-Jakob like syndrome during lithium carbonate treatment. Lithium serum level was within the therapeutic range. Complete clinical-electroencephalographic recovery was achieved after lithium therapy was discontinued.
B, Casanova, M, de Entrambasaguas, C, Perla, E, Gómez-Siurana, A, Benetó, J A, Burguera   +5 more
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Balint syndrome due to Creutzfeldt–Jakob disease

Neurology, 2004
Since Balint originally described a patient with striking disturbances in vision and movement,1 this syndrome has been reported to result from stroke, metastatic lesions, demyelinating disorders, carbon monoxide poisoning, corticobasal ganglionic degeneration, Alzheimer disease, and HIV infection.2 We report a patient with Balint syndrome resulting ...
B M, Ances, J M, Ellenbogen, S T, Herman, D, Jacobs, D S, Liebeskind, A, Chatterjee, S L, Galetta   +6 more
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Creutzfeldt-Jakob–Like Syndrome due to Hypercalcemic Encephalopathy

Clinical EEG and Neuroscience, 2014
Hypercalcemia can cause a subacute syndrome of progressive dementia and marked changes in the electroencephalogram (EEG). We report a case of iatrogenic hypercalcemia with a close correlation between the clinical course and the EEG changes. A 73-year-old woman presented with a subacute syndrome of progressive dementia and bursts of 1.5 to 2 Hz ...
Johannes, Rösche, Catharina, Sieveking, Christina, Kampf, Reiner, Benecke   +3 more
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Creutzfeldt-Jakob syndrome presenting as epilepsia partialis continua

Journal of Clinical Neuroscience, 2001
Creutzfeldt-Jakob disease (CJD) is an uncommon rapidly progressive neurological disorder which can have protean clinical presentations. We report an autopsy-proven case of CJD presenting initially as epilepsia partialis continua but then developing the typical clinical features of CJD over several weeks.
J, Parry, P, Tuch, W, Knezevic, V, Fabian   +3 more
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MRI Detection of the Cerebellar Syndrome in Creutzfeldt–Jakob Disease

The Cerebellum, 2009
Creutzfeldt-Jakob Disease (CJD) is characterized by bilateral basal ganglia hyperintensities on T2W and diffusion-weighted imaging (DWI) magnetic resonance imaging (MRI) scans, consistent with its extrapyramidal neurological manifestations. MRI is diagnostically uninformative about the cerebellar symptoms, equally prominent in CJD.
Oren S, Cohen, Chen, Hoffmann, Hedok, Lee, Joab, Chapman, Robert K, Fulbright, Isak, Prohovnik   +5 more
openaire   +2 more sources