Evidence map›Paper›PMID 42351535›Full record

ArticleDiagnostics (Basel, Switzerland)2026

Multisystemic Assessment in Andersen-Tawil Syndrome: Report of Eighteen Individuals.

Maria Gnazzo, Giovanni Parlapiano, Silvia Morlino, Mafalda Mucciolo, Daniele Minervino, Marco Castori, Francesca Mercadante, Michele Trifiletti, Maria Gabriela Obregon, Paolo Prontera and 8 more

Abstract read
In one paragraph

Article in Diagnostics (Basel, Switzerland), 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

18 authors.

Maria GnazzoLaboratory of Medical Genetics, Translational Cytogenomics Research Unit, Bambino Gesù Children's Hospital, IRCCS, 00165 Rome, Italy.ORCID 0000-0003-0764-686X
Giovanni ParlapianoCardiogenetic Center, Rare Diseases and Medical Genetics Units, Bambino Gesù Children's Hospital, IRCCS, 00165 Rome, Italy.ORCID 0000-0002-2275-9670
Silvia MorlinoDivision of Medical Genetics, Fondazione Casa Sollievo della Sofferenza, IRCCS, 71013 San Giovanni Rotondo, Italy.
Mafalda MuccioloLaboratory of Medical Genetics, Translational Cytogenomics Research Unit, Bambino Gesù Children's Hospital, IRCCS, 00165 Rome, Italy.ORCID 0000-0003-2228-8271
Daniele MinervinoLaboratory of Medical Genetics, Translational Cytogenomics Research Unit, Bambino Gesù Children's Hospital, IRCCS, 00165 Rome, Italy.
Marco CastoriDivision of Medical Genetics, Fondazione Casa Sollievo della Sofferenza, IRCCS, 71013 San Giovanni Rotondo, Italy.
Francesca MercadanteMedical Genetics Unit, Villa Sofia-Cervello Hospitals, 90146 Palermo, Italy.
Michele TrifilettiDepartment of Social Sciences, Universidad Católica San Antonio de Murcia (UCAM), 30107 Murcia, Spain.
Maria Gabriela ObregonGenetics Department, Hospital Garrahan, Buenos Aires C1245, Argentina.
Paolo PronteraMedical Genetics Unit, S. Maria della Misericordia Hospital, 06129 Perugia, Italy.
Daniela RighiPediatric Cardiology and Arrhythmia/Syncope Complex Unit, Bambino Gesù Children's Hospital, IRCCS, 00165 Rome, Italy.
Francesca Di LorenzoCardiogenetic Center, Rare Diseases and Medical Genetics Units, Bambino Gesù Children's Hospital, IRCCS, 00165 Rome, Italy.
Massimo Stefano SilvettiPediatric Cardiology and Arrhythmia/Syncope Complex Unit, Bambino Gesù Children's Hospital, IRCCS, 00165 Rome, Italy.
Maria Lisa DenticiRare Diseases and Medical Genetics Units, Bambino Gesù Children Hospital and Research Institute, IRCCS, 00165 Rome, Italy.ORCID 0000-0002-9505-5906
Andrea BartuliRare Diseases and Medical Genetics Units, Bambino Gesù Children Hospital and Research Institute, IRCCS, 00165 Rome, Italy.ORCID 0000-0001-9765-7460
Fabrizio DragoPediatric Cardiology and Arrhythmia/Syncope Complex Unit, Bambino Gesù Children's Hospital, IRCCS, 00165 Rome, Italy.ORCID 0000-0003-1888-373X
Antonio NovelliLaboratory of Medical Genetics, Translational Cytogenomics Research Unit, Bambino Gesù Children's Hospital, IRCCS, 00165 Rome, Italy.ORCID 0000-0002-9037-4297
Anwar BabanCardiogenetic Center, Rare Diseases and Medical Genetics Units, Bambino Gesù Children's Hospital, IRCCS, 00165 Rome, Italy.

Funding

Italian Ministry of Health PNRR-MCNT2-2023-12377263
6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

Andersen–Tawil SyndromeLong QTmultisystemic assessmentperiodic paralysis

Identifiers

PMID42351535
PMCPMC13298122

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.