Evidence map›Paper›PMID 33454496›Full record

ArticleClinical neurology and neurosurgery2021

Early sensory disturbances and seizures are common manifestations of familial Creutzfeldt-Jakob disease due to E200K PRNP mutation: Case report from two Peruvian families.

Elison Sarapura-Castro, Carlos Cosentino, Jonathan Landman, Avi Landman, Luis Torres, Yesenia Nuñez, Sabina Capellari, Piero Parchi, Mario Cornejo-Olivas

Open access · greenAbstract readCase Reports
PubMed Full text at PMC Publisher
In one paragraph

Article in Clinical neurology and neurosurgery, 2021. 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
–field-weighted citation impact, top 99% 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, 0 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

9 authors at 7 institutions in 3 countries.

Elison Sarapura-CastroNeurogenetics Research Center, Instituto Nacional de Ciencias Neurologicas, Lima, Peru; Northern Pacific Global Health Research Fellows Training Consortium, Seattle, USA; Master's Program in Clinical Epidemiology and Biostatistics, Universidad Científica del Sur, Lima, Peru. Electronic address: elison.sarapura.c@incngen.org.pe.
Carlos CosentinoMovement Disorders Unit, Instituto Nacional de Ciencias Neurologicas, Lima, Peru; School of Medicine, Universidad Nacional Mayor de San Marcos, Lima, Peru.
Jonathan LandmanDepartment of Neurology, University of Miami Miller School of Medicine, Miami, FL, USA.
Avi LandmanUniversity of Central Florida / HCA Healthcare Consortium, USA.
Luis TorresMovement Disorders Unit, Instituto Nacional de Ciencias Neurologicas, Lima, Peru; School of Medicine, Universidad Nacional Mayor de San Marcos, Lima, Peru.
Yesenia NuñezMovement Disorders Unit, Instituto Nacional de Ciencias Neurologicas, Lima, Peru.
Sabina CapellariIRCCS Istituto Delle Scienze Neurologiche Di Bologna, Bologna, Italy; Department of Biomedical and Neuromotor Sciences, University of Bologna, Bologna, Italy.
Piero ParchiIRCCS Istituto Delle Scienze Neurologiche Di Bologna, Bologna, Italy; Department of Experimental Diagnostic and Specialty Medicine (DIMES), University of Bologna, Bologna, Italy.
Mario Cornejo-OlivasNeurogenetics Research Center, Instituto Nacional de Ciencias Neurologicas, Lima, Peru; Center for Global Health, Universidad Peruana Cayetano Heredia, Lima, Peru.
Istituto delle Scienze Neurologiche di Bologna · ITNational University of San Marcos · PEInstituto Nacional de Ciencias NeurológicasUniversidad Científica del Sur · PEUniversidad Peruana Cayetano Heredia · PEUniversity of Central Florida · USUniversity of Miami · US

Funding

NPGH LEADERs YR12: OBSSR (Greenberg, Ngwafong Mukere) & NIBIB (Lee)D43TW009345 · FIC · UNIVERSITY OF WASHINGTON · PI Dibyadyuti Datta, Chandy C. John · 2017 to 2026
$15.2M
FIC NIH HHS D43 TW009345
6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

Creutzfeldt-Jakob SyndromeDiffusion Magnetic Resonance ImagingFemaleHumansMagnetic Resonance ImagingMaleMiddle AgedMutationParesthesiaPedigreePeruPrion ProteinsPrion ProteinsPRNP protein, humanCreutzfeldt-Jakob diseaseDementiaGeneticsSeizureSensory disturbance

Identifiers

PMID33454496
PMCPMC8023671
OpenAlexW3124290649

What OpenQuestion holds

Textmetadata
LicenceTDM
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.