Evidence map›Paper›PMID 38930051›Full record

ArticleJournal of clinical medicine2024

Exploring the Clinical and Genetic Landscape of Angelman Syndrome: Patient-Reported Insights from an Italian Registry.

Pier Luigi Carriero, Rosalia Zangari, Eleonora Sfreddo, Arianna Ghirardi, Arrigo Schieppati, Tiziano Barbui, Francesco Biroli

Abstract read
In one paragraph

Article in Journal of clinical medicine, 2024. 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. 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

7 authors.

Pier Luigi CarrieroFROM Research Foundation ETS, Papa Giovanni XXIII Hospital, 24127 Bergamo, Italy.
Rosalia ZangariFROM Research Foundation ETS, Papa Giovanni XXIII Hospital, 24127 Bergamo, Italy.ORCID 0000-0002-4425-7866
Eleonora SfreddoFROM Research Foundation ETS, Papa Giovanni XXIII Hospital, 24127 Bergamo, Italy.
Arianna GhirardiFROM Research Foundation ETS, Papa Giovanni XXIII Hospital, 24127 Bergamo, Italy.ORCID 0000-0001-9391-6963
Arrigo SchieppatiClinical Research Centre for Rare Diseases "Aldo and Cele Daccò", Mario Negri Institute for Pharmacological Research, 24020 Ranica, Italy.
Tiziano BarbuiFROM Research Foundation ETS, Papa Giovanni XXIII Hospital, 24127 Bergamo, Italy.
Francesco BiroliFROM Research Foundation ETS, Papa Giovanni XXIII Hospital, 24127 Bergamo, Italy.ORCID 0000-0002-0481-6520

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

Angelman syndromeepilepsygenotypematernal 15q11–q13 region deletionpatient-driven registrypatient registryrare disease

Identifiers

PMID38930051
PMCPMC11204522

What OpenQuestion holds

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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.