Evidence map›Paper›PMID 37443087›Full record

ArticleOrphanet journal of rare diseases2023

Correction to: implementation of second-tier tests in newborn screening for the detection of vitamin B12 related acquired and genetic disorders: results on 258,637 newborns.

Sonia Pajares, Jose Antonio Arranz, Aida Ormazabal, Mireia Del Toro, Ángeles García-Cazorla, Aleix Navarro-Sastre, Rosa María López, Silvia María Meavilla, Mariela Mercedes de Los Santos, Camila García-Volpe and 10 more

Open access · goldAbstract readPublished Erratum
PubMed Full text at PMC Publisher
In one paragraph

Article in Orphanet journal of rare diseases, 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
–field-weighted citation impact, top 84% 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

5 · Who and what money

Authors and funding

20 authors at 6 institutions in 1 country.

Sonia PajaresSección de Errores Congénitos del Metabolismo-IBC, Servicio de Bioquímica Y Genética Molecular, Hospital Clínic de Barcelona, C/ Mejía Lequerica S/N, Edificio Helios III, Barcelona, 08028, Spain.
Jose Antonio ArranzUnit of Metabolic Diseases, Hospital Vall D'Hebrón, Barcelona, Spain.
Aida OrmazabalCenter for Biomedical Research Network on Rare Diseases (CIBERER), Madrid, Spain.
Mireia Del ToroUnit of Metabolic Diseases, Hospital Vall D'Hebrón, Barcelona, Spain.
Ángeles García-CazorlaCenter for Biomedical Research Network on Rare Diseases (CIBERER), Madrid, Spain.
Aleix Navarro-SastreSección de Errores Congénitos del Metabolismo-IBC, Servicio de Bioquímica Y Genética Molecular, Hospital Clínic de Barcelona, C/ Mejía Lequerica S/N, Edificio Helios III, Barcelona, 08028, Spain.
Rosa María LópezSección de Errores Congénitos del Metabolismo-IBC, Servicio de Bioquímica Y Genética Molecular, Hospital Clínic de Barcelona, C/ Mejía Lequerica S/N, Edificio Helios III, Barcelona, 08028, Spain.
Silvia María MeavillaInborn Errors of Metabolism Unit, Hospital Sant Joan de Déu, Barcelona, Spain.
Mariela Mercedes de Los SantosInborn Errors of Metabolism Unit, Hospital Sant Joan de Déu, Barcelona, Spain.
Camila García-VolpeInborn Errors of Metabolism Unit, Hospital Sant Joan de Déu, Barcelona, Spain.
Jose Manuel González de Aledo-CastilloSección de Errores Congénitos del Metabolismo-IBC, Servicio de Bioquímica Y Genética Molecular, Hospital Clínic de Barcelona, C/ Mejía Lequerica S/N, Edificio Helios III, Barcelona, 08028, Spain.
Ana ArgudoSección de Errores Congénitos del Metabolismo-IBC, Servicio de Bioquímica Y Genética Molecular, Hospital Clínic de Barcelona, C/ Mejía Lequerica S/N, Edificio Helios III, Barcelona, 08028, Spain.
Jose Luís MarínSección de Errores Congénitos del Metabolismo-IBC, Servicio de Bioquímica Y Genética Molecular, Hospital Clínic de Barcelona, C/ Mejía Lequerica S/N, Edificio Helios III, Barcelona, 08028, Spain.
Clara CarnicerUnit of Metabolic Diseases, Hospital Vall D'Hebrón, Barcelona, Spain.
Rafael ArtuchCenter for Biomedical Research Network on Rare Diseases (CIBERER), Madrid, Spain.
Frederic TortSección de Errores Congénitos del Metabolismo-IBC, Servicio de Bioquímica Y Genética Molecular, Hospital Clínic de Barcelona, C/ Mejía Lequerica S/N, Edificio Helios III, Barcelona, 08028, Spain.
Laura GortSección de Errores Congénitos del Metabolismo-IBC, Servicio de Bioquímica Y Genética Molecular, Hospital Clínic de Barcelona, C/ Mejía Lequerica S/N, Edificio Helios III, Barcelona, 08028, Spain.
Rosa FernándezMaternal and Child Health Service, Public Health Agency of Catalonia, Health Department, Government of Catalonia, Barcelona, Spain.
Judit García-Villoria *Sección de Errores Congénitos del Metabolismo-IBC, Servicio de Bioquímica Y Genética Molecular, Hospital Clínic de Barcelona, C/ Mejía Lequerica S/N, Edificio Helios III, Barcelona, 08028, Spain.
Antonia Ribes *Sección de Errores Congénitos del Metabolismo-IBC, Servicio de Bioquímica Y Genética Molecular, Hospital Clínic de Barcelona, C/ Mejía Lequerica S/N, Edificio Helios III, Barcelona, 08028, Spain. aribes@clinic.cat.
Hospital Clínic de Barcelona · ESHospital Sant Joan de Déu Barcelona · ESCentre for Biomedical Network Research on Rare Diseases · ESVall d'Hebron Hospital Universitari · ESConsorci Institut D'Investigacions Biomediques August Pi I Sunyer · ESGeneralitat de Catalunya · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Identifiers

PMID37443087
PMCPMC10339513
OpenAlexW4384201294

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.