Quantitative EEG parameters correlate with the progression of human prion diseases. - Wikidata - wikimedia - TriplyDB

Quantitative EEG parameters correlate with the progression of human prion diseases.

Quantitative EEG parameters correlate with the progression of human prion diseases.

http://www.wikidata.org/entity/Q37282473

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Frail phenotype is associated with distinct quantitative electroencephalographic findings among end-stage renal disease patients: an observational study.

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Quantitative EEG parameters correlate with the progression of human prion diseases.

http://www.wikidata.org/entity/Q37282473

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article científic

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article scientifique

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articolo scientifico

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artigo científico

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bilimsel makale

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scientific article published on 13 July 2016

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vedecký článok

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vetenskaplig artikel

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videnskabelig artikel

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vědecký článek

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name

Quantitative EEG parameters correlate with the progression of human prion diseases.

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Quantitative EEG parameters correlate with the progression of human prion diseases.

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type

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Quantitative EEG parameters correlate with the progression of human prion diseases.

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Quantitative EEG parameters correlate with the progression of human prion diseases.

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prefLabel

Quantitative EEG parameters correlate with the progression of human prion diseases.

@en

Quantitative EEG parameters correlate with the progression of human prion diseases.

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JNNP-2016-313501

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Journal of Neurology, Neurosurgery and Psychiatry

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Quantitative EEG parameters correlate with the progression of human prion diseases.

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Andrew Thompson

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Jessica Lowe

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Joanna Kenny

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John Collinge

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Marie-Claire Porter

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Peter Rudge

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Simon Mead

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Creative Commons Attribution

P2860

Prion diseases of humans and animals: their causes and molecular basis

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Ultrasensitive human prion detection in cerebrospinal fluid by real-time quaking-induced conversion.

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Sporadic and familial CJD: classification and characterisation.

Slowing of EEG background activity in Parkinson's and Alzheimer's disease with early cognitive dysfunction

EEG dynamics in patients with Alzheimer's disease.

EEG in Creutzfeldt-Jakob disease.

A systematic review of prion therapeutics in experimental models.

Updated clinical diagnostic criteria for sporadic Creutzfeldt-Jakob disease.

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10.1136/JNNP-2016-313501

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Prion protein family

transmissible spongiform encephalopathy

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