Evidence map›Paper›PMID 35465339›Full record

ArticleActa myologica : myopathies and cardiomyopathies : official journal of the Mediterranean Society of Myology2022

Frailties and critical issues in neuromuscular diseases highlighted by SARS-CoV-2 pandemic: how many patients are still "invisible"?

Giulia Ricci, Francesca Torri, Francesca Bianchi, Lorenzo Fontanelli, Erika Schirinzi, Elisa Gualdani, Paolo Francesconi, Delia Gagliardi, Gigliola Serra, Tiziana Mongini and 1 more

Open access · greenAbstract read
In one paragraph

Article in Acta myologica : myopathies and cardiomyopathies : official journal of the Mediterranean Society of Myology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.7field-weighted citation impact, top 29% of its field
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

6 citing papers in PubMed, 6 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Observational
  5. Article
  6. 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

11 authors at 3 institutions in 1 country.

Giulia RicciDepartment of Clinical and Experimental Medicine, University of Pisa, Pisa, Italy.
Francesca TorriDepartment of Clinical and Experimental Medicine, University of Pisa, Pisa, Italy.
Francesca BianchiDepartment of Clinical and Experimental Medicine, University of Pisa, Pisa, Italy.
Lorenzo FontanelliDepartment of Clinical and Experimental Medicine, University of Pisa, Pisa, Italy.
Erika SchirinziDepartment of Clinical and Experimental Medicine, University of Pisa, Pisa, Italy.
Elisa GualdaniAgenzia Regionale Toscana, ARS.
Paolo FrancesconiAgenzia Regionale Toscana, ARS.
Delia GagliardiFoundation IRCCS Ca' Granda Ospedale Maggiore Policlinico, Neurology Unit, Milan, Italy.
Gigliola SerraClinica di Neuropsichiatria Infantile, Dipartimento di Scienze Mediche, Chirurgiche e Sperimentali, Università degli Studi di Sassari, Sassari, Italy.
Tiziana MonginiDepartment of Neurosciences Rita Levi Montalcini, Università degli Studi di Torino, Torino, Italy.
Gabriele SicilianoDepartment of Clinical and Experimental Medicine, University of Pisa, Pisa, Italy.
University of Pisa · ITFondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico · ITUniversity of Turin · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Almost 90% of neuromuscular diseases (NMDs) are classified as rare diseases, defined as conditions affecting less than 5 individuals in 10.000 (0.05%). Their rarity and diversity pose specific challenges for healthcare and research. Epidemiological data on NMDs are often lacking and incomplete. The COVID-19 pandemic has further highlighted the management difficulties of NMDs patients and the necessity to continue the program of implementation of standard of care. This article summarizes the Italian experience during pandemic.

Indexed as

COVID-19FrailtyNeuromuscular DiseasesHumansPandemicsSARS-CoV-2COVID-19 pandemicneuromuscular diseases

Identifiers

PMID35465339
PMCPMC9004333
OpenAlexW4224861617

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.