Evidence map›Paper›PMID 33763332›Full record

ArticleMolecular genetics and metabolism reports2021

Evaluation of 3-

Francyne Kubaski, Zackary M Herbst, Danilo A A Pereira, Camilo Silva, Christine Chen, Paul W L Hwu, Helio van der Linden, Charles M Lourenço, Roberto Giugliani

Erratum issuedOpen access · goldAbstract read
PubMed Full text at PMC Publisher
In one paragraph

Article in Molecular genetics and metabolism reports, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 5 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed, 1 pooled it
0.7field-weighted citation impact, top 35% 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

5 citing papers in PubMed, 1 synthesis or guideline pooled it, 5 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Review
  4. Gene therapy for neurotransmitter-related disorders.Journal of inherited metabolic disease · 2024
    Review
  5. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

9 authors at 4 institutions in 3 countries.

Francyne KubaskiPPGBM, UFRGS, Porto Alegre, Brazil.
Zackary M HerbstDepartment of Chemistry, University of Washington, Seattle, USA.
Danilo A A PereiraDepartment of Research and Innovation, Innovatox, São Paulo, Brazil.
Camilo SilvaWaters Technologies do Brasil Ltda, São Paulo, Brazil.
Christine ChenNational Taiwan University Hospital, Taipei, Taiwan.
Paul W L HwuNational Taiwan University Hospital, Taipei, Taiwan.
Helio van der LindenCentro de Reabilitação Dr Henrique Santillo, Goiânia, Brazil.
Charles M LourençoCentro Universitário Estácio, Ribeirão Preto, Brazil.
Roberto GiuglianiPPGBM, UFRGS, Porto Alegre, Brazil.
National Taiwan University Hospital · TWHospital de Clínicas de Porto Alegre · BRUniversidade Federal do Rio Grande do Sul · BRUniversity of Washington · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Aromatic L-amino acid decarboxylase (AADCD) deficiency is an autosomal recessive neurometabolic disorder, caused by biallelic mutations in the

Indexed as

3-O-methyldopaAromatic L-amino acid decarboxylase deficiencyLiquid chromatography tandem mass spectrometryNewborn screening

Identifiers

PMID33763332
PMCPMC7973244
OpenAlexW3136423898

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.