Evidence map›Paper›PMID 38410281›Full record

ArticleGlobal health, epidemiology and genomics2024

Baseline Characteristics of Fabry Disease "Amenable" Migalastat Patients in Argentinian Cohort.

Sebastián Jaurretche, Santiago Alonso, Mónica Calvo, Sebastián Fernandez, Heber Figueredo, Beatriz Galli, Ivanna Marin, Andrés Martinez, Silvia Mattausch, Fernando Perretta and 3 more

Open access · goldAbstract read
In one paragraph

Article in Global health, epidemiology and genomics, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed, 1 pooled it
0.3field-weighted citation impact, top 44% 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

2 citing papers in PubMed, 1 synthesis or guideline pooled it, 1 citations in OpenAlex.

  1. Pooled it
  2. Article
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

13 authors at 6 institutions in 1 country.

Sebastián JaurretcheTransplant Department, Sanatorio Parque de Rosario, Rosario, Argentina.ORCID 0000-0002-1462-2703
Santiago AlonsoAngel C. Padilla Hospital, San Miguel de Tucumán, Argentina.
Mónica CalvoSTR Cuidadela, Buenos Aires, Argentina.
Sebastián FernandezInstituto de Nefrología y Hemodiálisis, Mendoza, Argentina.
Heber FigueredoRheumatology Department, Juan Domingo Perón Hospital, Formosa, Argentina.
Beatriz GalliSan Bernardo Hospital, Salta, Argentina.
Ivanna MarinCentral Hospital, Mendoza, Argentina.
Andrés MartinezCentral Hospital, San Luis, Argentina.
Silvia MattauschFresenius Medical Care, Córdoba, Argentina.
Fernando PerrettaIntensive Care Unit, Dr. Enrique Erill Hospital, Belén de Escobar, Buenos Aires, Argentina.
Juan PoliteiNeurology Department, SPINE Foundation, Buenos Aires, Argentina.
Juan Ignacio RolonGerman Hospital, Buenos Aires, Argentina.
Esteban CalabreseINECO, Neurociencias Oroño, Rosario, Argentina.
Centro Científico Tecnólogico - Rosario · ARCentro Científico Tecnológico - San Luis · ARFavaloro Foundation · ARInstituto de Histología y Embriología de Mendoza · ARInstituto de Neurología Cognitiva · ARUniversity of Mendoza · AR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Fabry disease (FD) is a multisystem lysosomal storage disorder induced by genetic variants in the alpha-galactosidase A (

Indexed as

Fabry Disease1-DeoxynojirimycinAdultalpha-GalactosidaseFemaleHumansMalePain1-Deoxynojirimycinalpha-Galactosidasemigalastat

Identifiers

PMID38410281
PMCPMC10896645
OpenAlexW4391923216

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.