Evidence map›Paper›PMID 38510379›Full record

ArticleFrontiers in neurology2024

Corrigendum: Newborn screening for X-linked adrenoleukodystrophy in Italy: diagnostic algorithm and disease monitoring.

Eleonora Bonaventura, Luisella Alberti, Simona Lucchi, Laura Cappelletti, Salvatore Fazzone, Elisa Cattaneo, Matteo Bellini, Giana Izzo, Cecilia Parazzini, Alessandra Bosetti and 14 more

Abstract readPublished Erratum
In one paragraph

Article in Frontiers in neurology, 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
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

5 · Who and what money

Authors and funding

24 authors.

Eleonora BonaventuraChild Neurology Unit, V. Buzzi Children's Hospital, Milan, Italy.
Luisella AlbertiCenter for Diagnosis and Treatment of Leukodystrophies and Genetic Leukoencephalopathies (COALA), V. Buzzi Children's Hospital, Milan, Italy.
Simona LucchiNewborn Screening and Inherited Metabolic Disease Unit, V. Buzzi Children Hospital, Milan, Italy.
Laura CappellettiNewborn Screening and Inherited Metabolic Disease Unit, V. Buzzi Children Hospital, Milan, Italy.
Salvatore FazzoneNewborn Screening and Inherited Metabolic Disease Unit, V. Buzzi Children Hospital, Milan, Italy.
Elisa CattaneoCenter for Diagnosis and Treatment of Leukodystrophies and Genetic Leukoencephalopathies (COALA), V. Buzzi Children's Hospital, Milan, Italy.
Matteo BelliniMolecular Genetics Laboratory, ASST Papa Giovanni XXIII, Bergamo, Italy.
Giana IzzoCenter for Diagnosis and Treatment of Leukodystrophies and Genetic Leukoencephalopathies (COALA), V. Buzzi Children's Hospital, Milan, Italy.
Cecilia ParazziniCenter for Diagnosis and Treatment of Leukodystrophies and Genetic Leukoencephalopathies (COALA), V. Buzzi Children's Hospital, Milan, Italy.
Alessandra BosettiCenter for Diagnosis and Treatment of Leukodystrophies and Genetic Leukoencephalopathies (COALA), V. Buzzi Children's Hospital, Milan, Italy.
Elisabetta Di ProfioDepartment of Paediatrics, V. Buzzi Children's Hospital, University of Milan, Milan, Italy.
Giulia FioreDepartment of Paediatrics, V. Buzzi Children's Hospital, University of Milan, Milan, Italy.
Matilde FerrarioCenter for Diagnosis and Treatment of Leukodystrophies and Genetic Leukoencephalopathies (COALA), V. Buzzi Children's Hospital, Milan, Italy.
Chiara MameliCenter for Diagnosis and Treatment of Leukodystrophies and Genetic Leukoencephalopathies (COALA), V. Buzzi Children's Hospital, Milan, Italy.
Arianna SangiorgioDepartment of Paediatrics, V. Buzzi Children's Hospital, University of Milan, Milan, Italy.
Silvia MasnadaChild Neurology Unit, V. Buzzi Children's Hospital, Milan, Italy.
Gian Vincenzo ZuccottiDepartment of Paediatrics, V. Buzzi Children's Hospital, University of Milan, Milan, Italy.
Pierangelo VeggiottiChild Neurology Unit, V. Buzzi Children's Hospital, Milan, Italy.
Luigina SpacciniCenter for Diagnosis and Treatment of Leukodystrophies and Genetic Leukoencephalopathies (COALA), V. Buzzi Children's Hospital, Milan, Italy.
Maria IasconeMolecular Genetics Laboratory, ASST Papa Giovanni XXIII, Bergamo, Italy.
Elvira VerduciCenter for Diagnosis and Treatment of Leukodystrophies and Genetic Leukoencephalopathies (COALA), V. Buzzi Children's Hospital, Milan, Italy.
Cristina CeredaCenter for Diagnosis and Treatment of Leukodystrophies and Genetic Leukoencephalopathies (COALA), V. Buzzi Children's Hospital, Milan, Italy.
Davide TondutiChild Neurology Unit, V. Buzzi Children's Hospital, Milan, Italy.
XALD-NBS Study Group

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

[This corrects the article DOI: 10.3389/fneur.2022.1072256.].

Indexed as

Aicardi-Goutières syndrome (AGS)C26:0-lysophosphatidylcholineDBShematopoietic stem cell transplantation (HCST)newborn screening (NBS)X-ALDX-linked adrenoleukodystrophy (X-ALD)Zellweger Spectrum Disorders

Identifiers

PMID38510379
PMCPMC10953821

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.