Results 141 to 150 of about 21,599 (190)

Palliative care symptoms of people living with rapidly progressive prion diseases: a systematic review. [PDF]

open access: yesBMC Palliat Care
Williams RT   +9 more
europepmc   +1 more source

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

open access: yesActa Neuropathol Commun
Bentivenga GM   +11 more
europepmc   +1 more source

A critical perspective of prion disease surveillance in Brazil. [PDF]

open access: yesFront Neurosci
Barbosa BJAP   +2 more
europepmc   +1 more source

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

open access: yesTidsskrift for den Norske laegeforening : tidsskrift for praktisk medicin, ny raekke, 1996
openaire   +1 more source
Some of the next articles are maybe not open access.

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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   +5 more
openaire   +3 more sources

Sjögren syndrome presenting with encephalopathy mimicking Creutzfeldt–Jakob disease

Journal of the Neurological Sciences, 2013
A 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.
Koushun Matsuo   +2 more
exaly   +3 more sources

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