Evidence map›Paper›PMID 37701328›Full record

ArticleJIMD reports2023

Development of tools to facilitate the diagnosis of hereditary fructose intolerance.

Bianca Panis, Lise E F Janssen, Dirk J Lefeber, Nynke Simons, M Estela Rubio-Gozalbo, Martijn C G J Brouwers

Open access · goldAbstract read
In one paragraph

Article in JIMD reports, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
1.0field-weighted citation impact, top 22% 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

3 citing papers in PubMed, 5 citations in OpenAlex.

  1. Review
  2. Article
  3. 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

6 authors at 3 institutions in 1 country.

Bianca PanisDivision of Genetic Metabolic Diseases, Department of Pediatrics Maastricht University Medical Center Maastricht The Netherlands.ORCID https://orcid.org/0000-0001-5953-139X
Lise E F JanssenDivision of Endocrinology and Metabolic Diseases, Department of Internal Medicine Maastricht University Medical Center Maastricht The Netherlands.
Dirk J LefeberTranslational Metabolic Laboratory, Department of Laboratory Medicine Radboud University Medical Center Nijmegen The Netherlands.
Nynke SimonsDivision of Endocrinology and Metabolic Diseases, Department of Internal Medicine Maastricht University Medical Center Maastricht The Netherlands.
M Estela Rubio-GozalboDivision of Genetic Metabolic Diseases, Department of Pediatrics Maastricht University Medical Center Maastricht The Netherlands.
Martijn C G J BrouwersMember of European Reference Network for Hereditary Metabolic Diseases (MetabERN).ORCID https://orcid.org/0000-0002-8229-3331
Maastricht University Medical Centre · NLMaastricht University · NLRadboud University Nijmegen · NL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Although hereditary fructose intolerance (HFI) is an inborn error of fructose metabolism that classically presents at infancy, the diagnosis is often missed or delayed. In this study, we aimed to develop tools to facilitate the diagnosis of HFI. The intake of fructose-containing food products, that is, fruit, fruit juice and sugar-sweetened beverages, was assessed by a 3-day food diary in adult HFI patients (

Indexed as

food diaryfructoseglycosylation of transferrinhereditary fructose intolerance (HFI)

Identifiers

PMID37701328
PMCPMC10494505
OpenAlexW4385365030

What Socratic 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 Socratic graph.