Evidence map›Paper›PMID 38010785›Full record

ReviewRevista de neurologia2023

[The new age of neurodegenerative diseases. The basis of the new approaches].

G García-Ribas, P Garay-Albizuri, E S Stiauren-Fernández, F Pérez-Trapote, M A Zea-Sevilla

Open access · greenAbstract readEnglish AbstractReview
In one paragraph

Review in Revista de neurologia, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
0.2field-weighted citation impact, top 43% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed, 2 citations in OpenAlex.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors at 4 institutions in 1 country.

G García-RibasHospital Universitario Ramón y Cajal, 28034 Madrid, España.
P Garay-AlbizuriHospital Universitario Ramón y Cajal, 28034 Madrid, España.
E S Stiauren-FernándezHospital Universitario HM Sanchinarro, Madrid, España.
F Pérez-TrapoteHospital Universitario Ruber Juan Bravo, Madrid, España.
M A Zea-SevillaFindación CIEN. Instituto de Salud Carlos III, Madrid, España.
Hospital Universitario Ramón y Cajal · ESHospital Ruber Internacional · ESHospital Universitario HM Sanchinarro · ESInstituto de Salud Carlos III · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The detection by biomarkers of the pathophysiological and molecular processes involved in misfolding protein diseases making it possible to delineate the natural history of these processes. The great majority of protein misfolding diseases have a prolonged preclinical phase, in which the biological changes are patent. The clinical manifestations (i.e., phenotypes) do not have a univocal correspondence with the underlying pathology, despite the fact that pathological eponyms have been used for the description of the clinical syndromes, which has favored diagnostic inaccuracy. In order to perform an adequate clinical management, we must know the 3 planes that currently define the most common neurodegenerative processes. Diagnostic accuracy will be a prerequisite for new therapies aimed at modifying the course of brain protein misfolding diseases.

Indexed as

Neurodegenerative DiseasesProteostasis DeficienciesBiomarkersHumansProteinsBiomarkersProteins

Identifiers

PMID38010785
PMCPMC10831702
OpenAlexW4389099233

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.