Evidence map›Paper›PMID 37744437›Full record

ArticleFrontiers in pediatrics2023

Case report: Structural brain abnormalities in

Piero Pavone, Pasquale Striano, Giovanni Cacciaguerra, Simona Domenica Marino, Enrico Parano, Xena Giada Pappalardo, Raffaele Falsaperla, Martino Ruggieri

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

Article in Frontiers in pediatrics, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing 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

7 citing papers in PubMed.

  1. Article
  2. Review
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  4. Review
  5. Article
  6. Article
  7. Lissencephaly caused by aFrontiers in pediatrics · 2024
    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

8 authors.

Piero PavoneSection of Pediatrics and Child Neuropsychiatry, Department of Child and Experimental Medicine, University of Catania, Catania, Italy.
Pasquale StrianoDepartment of Neurosciences, Rehabilitation, Ophthalmology, Genetics, Maternal and Child Health, University of Genoa, Genova, Italy.
Giovanni CacciaguerraSection of Pediatrics and Child Neuropsychiatry, Department of Child and Experimental Medicine, University of Catania, Catania, Italy.
Simona Domenica MarinoPediatrics and Pediatric Emergency Department, University Hospital, A.U.O "Policlinico-Vittorio Emanuele", Catania, Italy.
Enrico ParanoNational Council of Research, Institute for Biomedical Research and Innovation (IRIB), Unit of Catania, Catania, Italy.
Xena Giada PappalardoNational Council of Research, Institute for Biomedical Research and Innovation (IRIB), Unit of Catania, Catania, Italy.
Raffaele FalsaperlaPediatrics and Pediatric Emergency Department, University Hospital, A.U.O "Policlinico-Vittorio Emanuele", Catania, Italy.
Martino RuggieriSection of Pediatrics and Child Neuropsychiatry, Department of Child and Experimental Medicine, University of Catania, Catania, Italy.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Tubulin genes have been related to severe neurological complications and the term "tubulinopathy" now refers to a heterogeneous group of disorders involving an extensive family of tubulin genes with Methods: A literature review of the cases of Results: Clinical manifestations of Discussion: A range of clinical manifestations related to different cerebral structures involved may be observed in patients with

Indexed as

cerebral anomaliesDandy–Walker MalformationDWM phenotypeTUBA1A-tubulinopathytubulinopathies

Identifiers

PMID37744437
PMCPMC10515619

What OpenQuestion holds

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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.