Evidence map›Paper›PMID 42652823›Full record

ArticleJournal of clinical medicine2026

Glucose Transporter Type 1 Deficiency Syndrome: Clinical Variability and Challenges in Ketogenic Diet Management in a Paediatric Case Series.

Mariana Viegas, Nanci Baptista, Fátima Martins, Joana Almeida, Cristina Pereira, Filipa Rodrigues, Joana Salgado, Joana Ribeiro, Sara Ferreira, Rui Diogo

Abstract read
PubMed Full text at PMC Publisher
In one paragraph

Article in Journal of clinical medicine, 2026. 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
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.

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

10 authors.

Mariana ViegasInherited Metabolic Diseases Reference Centre, Coimbra Local Health Unit, MetabERN, 3004-561 Coimbra, Portugal.ORCID 0000-0002-6697-9763
Nanci BaptistaInherited Metabolic Diseases Reference Centre, Coimbra Local Health Unit, MetabERN, 3004-561 Coimbra, Portugal.
Fátima MartinsInherited Metabolic Diseases Reference Centre, Coimbra Local Health Unit, MetabERN, 3004-561 Coimbra, Portugal.
Joana AlmeidaInherited Metabolic Diseases Reference Centre, Coimbra Local Health Unit, MetabERN, 3004-561 Coimbra, Portugal.
Cristina PereiraCoimbra Local Health Unit, Department of Paediatric Neurology, Paediatric Hospital of Coimbra, 3000-602 Coimbra, Portugal.
Filipa RodriguesNeurodevelopment Unit, Aveiro Local Health Unit, Department of Paediatrics, 3814-501 Aveiro, Portugal.ORCID 0000-0001-9165-2159
Joana SalgadoCoimbra Local Health Unit, Department of Medical Genetics, Paediatric Hospital of Coimbra, 3000-602 Coimbra, Portugal.
Joana RibeiroCoimbra Local Health Unit, Department of Paediatric Neurology, Paediatric Hospital of Coimbra, 3000-602 Coimbra, Portugal.
Sara FerreiraInherited Metabolic Diseases Reference Centre, Coimbra Local Health Unit, MetabERN, 3004-561 Coimbra, Portugal.
Rui DiogoInherited Metabolic Diseases Reference Centre, Coimbra Local Health Unit, MetabERN, 3004-561 Coimbra, Portugal.ORCID 0009-0006-6236-7926

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

epilepsyglucose transporter type 1 deficiency syndromeketogenic dietmovement disordersSLC2A1

Identifiers

PMID42652823
PMCPMC13514181

What OpenQuestion holds

Textmetadata
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.