Evidence map›Paper›PMID 24765480›Full record

ArticleClinics and practice2012

Optic nerve enlargement in infantile form of Krabbe disease.

Dimas Castilha-Neto, Letícia Fernandes Monteiro, Mirella Maccarini Peruchi, João Moreno Filho, Aline Vieira Scarlatelli-Lima, Jaime Lin

Abstract readCase Reports
PubMed Full text at PMC Publisher
In one paragraph

Article in Clinics and practice, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Inborn errors of metabolism.Handbook of clinical neurology · 2019
    Review
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.

Dimas Castilha-NetoDepartment of Biology, Health and Social Sciences, Universidade do Sul de Santa Catarina (UNISUL);
Letícia Fernandes MonteiroDepartment of Biology, Health and Social Sciences, Universidade do Sul de Santa Catarina (UNISUL);
Mirella Maccarini PeruchiDepartment of Radiology, Hospital São João Batista;
João Moreno FilhoDepartment of Radiology, Hospital Nossa Senhora da Conceição, Brazil.
Aline Vieira Scarlatelli-LimaDepartment of Biology, Health and Social Sciences, Universidade do Sul de Santa Catarina (UNISUL);
Jaime LinDepartment of Biology, Health and Social Sciences, Universidade do Sul de Santa Catarina (UNISUL);

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Krabbe disease (KD) is an autosomal recessive lysosomal storage disorder caused by dysfunctional galactosylceramidase activity. Infantile form is the most common subtype, occurring at about 6-month of age. We present a rare case of infantile KD with magnetic resonance imaging showing white matter, thalamic and basal ganglia lesions rarely associated with an enlargement of the optic nerves bilaterally.

Indexed as

galactosylceramidasegloboid cell leukodystrophyKrabbe diseaseoptic nerve enlargementstorage disorder.

Identifiers

PMID24765480
PMCPMC3981200

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.