An Atypical Presentation of Sporadic Creutzfeldt-Jakob Disease in the Setting of Chronic Alcohol Use Disorder. [PDF]
Holt C +3 more
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Comprehensive Review of Anesthetic Strategies for Patients With Neurodegenerative Diseases. [PDF]
Grabarczyk Ł.
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Palliative care symptoms of people living with rapidly progressive prion diseases: a systematic review. [PDF]
Williams RT +9 more
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Lurking in Ambush: A Case Report of Probable Creutzfeldt-Jakob Disease From Rural Kerala, India. [PDF]
Georgy I +4 more
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Distinct cerebrospinal fluid proteomic signatures define clinicopathological subtypes of sporadic Creutzfeldt-Jakob disease and predict patient survival. [PDF]
Bentivenga GM +11 more
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A critical perspective of prion disease surveillance in Brazil. [PDF]
Barbosa BJAP +2 more
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[Creutzfeldt-Jakob syndrome. A new variant in Great Britain].
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Related searches:
Lithium-Induced Creutzfeldt-Jakob Syndrome
Clinical Neuropharmacology, 1996a 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 +5 more
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Sjögren syndrome presenting with encephalopathy mimicking Creutzfeldt–Jakob disease
Journal of the Neurological Sciences, 2013A 61-year-old man developed subacute progressive dementia, general fatigue, a tonic-clonic seizure, and a decreased level of consciousness. He had a past history of chronic hepatitis type C and was diagnosed as having hepatic encephalopathy due to hyperammonemia.
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