Evidence map›Paper›PMID 38370996›Full record

ArticleCureus2024

The Clinical Spectrum of Adrenoleukodystrophy at a Portuguese Tertiary Hospital: Case Series and Review of Literature.

Catarina Menezes, Ana Losa, Sara Mosca, Ana de Carvalho Vaz, Catarina M Figueiredo, Cristina Garrido, Teresa Borges, Joana Borges Correia

Open access · diamondAbstract readCase Reports
In one paragraph

Article in Cureus, 2024. 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 99% 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

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

8 authors at 2 institutions in 1 country.

Catarina MenezesPediatrics, Centro Materno Infantil do Norte - Centro Hospitalar Universitário de Santo António, Porto, PRT.
Ana LosaPediatrics, Centro Materno Infantil do Norte - Centro Hospitalar Universitário de Santo António, Porto, PRT.
Sara MoscaPediatrics, Centro Materno Infantil do Norte - Centro Hospitalar Universitário de Santo António, Porto, PRT.
Ana de Carvalho VazPediatrics, Centro Materno Infantil do Norte - Centro Hospitalar Universitário de Santo António, Porto, PRT.
Catarina M FigueiredoPediatric Endocrinology, Centro Hospitalar Entre Douro e Vouga, Santa Maria da Feira, PRT.
Cristina GarridoPediatric Neurology, Centro Materno Infantil do Norte - Centro Hospitalar Universitário de Santo António, Porto, PRT.
Teresa BorgesPediatric Endocrinology, Centro Materno Infantil do Norte - Centro Hospitalar Universitário de Santo António, Porto, PRT.
Joana Borges CorreiaPediatrics, Reference Centre for Metabolic Disorders, Centro Materno Infantil do Norte - Centro Hospitalar Universitário de Santo António, Porto, PRT.
Centro Hospitalar do Porto · PTUnidade Local de Saúde de Entre Douro e Vouga · PT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Adrenoleukodystrophy, a rare genetic disease associated with the X chromosome (X-ALD - X-linked adrenoleukodystrophy), predominantly affects males and stems from mutations in the

Indexed as

adrenal insufficiency (ai)cerebral x-linked adrenoleukodystrophydemyelinating disordersperoxisomal disordersx- linked adrenoleukodystrophy

Identifiers

PMID38370996
PMCPMC10874197
OpenAlexW4391043736

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.