Evidence map›Paper›PMID 28344438›Full record

ReviewActa myologica : myopathies and cardiomyopathies : official journal of the Mediterranean Society of Myology2016

Learning disabilities in neuromuscular disorders: a springboard for adult life.

Guja Astrea, Roberta Battini, Sara Lenzi, Silvia Frosini, Silvia Bonetti, Elena Moretti, Silvia Perazza, Filippo M Santorelli, Chiara Pecini

Open access · greenAbstract readReview
In one paragraph

Review in Acta myologica : myopathies and cardiomyopathies : official journal of the Mediterranean Society of Myology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
0.3field-weighted citation impact, top 30% 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

10 citing papers in PubMed, 15 citations in OpenAlex.

  1. Article
  2. Marked neuropsychiatric involvement and dysmorphic features in nemaline myopathy.Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology · 2024
    Article
  3. Article
  4. Article
  5. Review
  6. Review
  7. Cognitive Deficits in Myopathies.International journal of molecular sciences · 2020
    Review
  8. Article
  9. Article
  10. Duchenne and Becker muscular dystrophy in adolescents: current perspectives.Adolescent health, medicine and therapeutics · 2018
    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

9 authors at 1 institution in 1 country.

Guja AstreaDepartmet of Developmental Neuroscience, IRCCS Fondazione Stella Maris, Pisa.
Roberta BattiniDepartmet of Developmental Neuroscience, IRCCS Fondazione Stella Maris, Pisa.
Sara LenziDepartmet of Developmental Neuroscience, IRCCS Fondazione Stella Maris, Pisa.
Silvia FrosiniDepartmet of Developmental Neuroscience, IRCCS Fondazione Stella Maris, Pisa.
Silvia BonettiDepartmet of Developmental Neuroscience, IRCCS Fondazione Stella Maris, Pisa.
Elena MorettiDepartmet of Developmental Neuroscience, IRCCS Fondazione Stella Maris, Pisa.
Silvia PerazzaDepartmet of Developmental Neuroscience, IRCCS Fondazione Stella Maris, Pisa.
Filippo M SantorelliMolecular Medicine, IRCCS Fondazione Stella Maris, Pisa.
Chiara PeciniDepartmet of Developmental Neuroscience, IRCCS Fondazione Stella Maris, Pisa.
Fondazione Stella Maris · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Although the presence of cognitive deficits in Duchenne muscular dystrophy or myotonic dystrophy DM1 is well established in view of brain-specific expression of affected muscle proteins, in other neuromuscular disorders, such as congenital myopathies and limb-girdle muscular dystrophies, cognitive profiles are poorly defined. Also, there are limited characterization of the cognitive profile of children with congenital muscular dystrophies, notwithstanding the presence of cerebral abnormality in some forms, and in spinal muscular atrophies, with the exception of distal spinal muscular atrophy (such as the DYN1CH1- associated form). Starting from the Duchenne muscular dystrophy, which may be considered a kind of paradigm for the co-occurrence of learning disabilities in the contest of a progressive muscular involvement, the findings of neuropsychological (or cognitive) dysfunctions in several forms of neuromuscular diseases will be examined and reviewed.

Indexed as

HumansIntellectual DisabilityLearning DisabilitiesMuscular DiseasesMuscular DystrophiesMuscular Dystrophies, Limb-GirdleMuscular Dystrophy, DuchenneMyotonic DystrophySpinal Muscular Atrophies of ChildhoodCMCMDDMDlearning disasbilitySMA-LED

Identifiers

PMID28344438
PMCPMC5343745
OpenAlexW2604199034

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.