Cerebrospinal fluid biomarkers in human genetic transmissible spongiform encephalopathies (Q34901990)

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28 January 2020

title

Cerebrospinal fluid biomarkers in human genetic transmissible spongiform encephalopathies (English)

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28 January 2020

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12

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Natividad Cuadrado Corrales

28 January 2020

5

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28 January 2020

Raquel Sanchez-Valle

6

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28 January 2020

Adriano Aguzzi

8

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28 January 2020

Theodoros Sklaviadis

9

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28 January 2020

Miguel Calero

13

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28 January 2020

Maurizio Pocchiari

15

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Inga Zerr

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28 January 2020

Cornelia M. van Duijn

14

object named as

Cornelia M van Duijn

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28 January 2020

10

Jerzy Kulczycki

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28 January 2020

16

Richard Knight

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28 January 2020

4

Alison Green

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28 January 2020

author name string

Anna Ladogana

1

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28 January 2020

Pascual Sanchez-Juan

2

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28 January 2020

Eva Mitrová

3

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28 January 2020

Silvia Koscova

7

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28 January 2020

Joanna Gawinecka

11

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28 January 2020

publication date

15 May 2009

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28 January 2020

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19444528%20AND%20SRC:MED&resulttype=core&format=json

28 January 2020

volume

256

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page(s)

1620-1628

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28 January 2020

issue

10

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https://scigraph.springernature.com/pub.10.1007/s00415-009-5163-x

28 January 2020

exact match

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cites work

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Cerebrospinal fluid biomarkers in Creutzfeldt-Jakob disease

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A prospective study of CSF markers in 250 patients with possible Creutzfeldt-Jakob disease

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Decreased beta-amyloid1-42 and increased tau levels in cerebrospinal fluid of patients with Alzheimer disease

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Mutations of the prion protein gene phenotypic spectrum

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Clinically atypical CJD: diagnostic relevance of cerebrospinal fluid markers and molecular genetic analysis?

8 July 2018

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Clinicopathological characteristics of Creutzfeldt-Jakob disease with a PrP V180I mutation and M129V polymorphism on different alleles

8 July 2018

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Creutzfeldt-Jakob disease associated with the R208H mutation in the prion protein gene

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Tau protein and 14-3-3 protein in the differential diagnosis of Creutzfeldt-Jakob disease

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Phenotypic variability in fatal familial insomnia (D178N-129M) genotype.

21 January 2018

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The diagnostic efficiency of biomarkers in sporadic Creutzfeldt-Jakob disease compared to Alzheimer's disease.

21 January 2018

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Creutzfeldt-Jakob disease in a patient with an R208H mutation of the prion protein gene (PRNP) and a 17-kDa prion protein fragment

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10.1007/S00415-009-5163-X

Identifiers

DOI

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Dimensions Publication ID

28 January 2020

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28 January 2020

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