Evidence map›Paper›PMID 34184449›Full record

ArticleJournal of clinical neurology (Seoul, Korea)2021

Nemaline Rod/Cap Myopathy Due to Novel Homozygous

Kiran Polavarapu, Mainak Bardhan, Ram Murthy Anjanappa, Seena Vengalil, Veeramani Preethish-Kumar, Leena Shingavi, Tanushree Chawla, Saraswati Nashi, Dhaarini Mohan, Gautham Arunachal and 3 more

Open access · diamondAbstract read
PubMed Full text at PMC Publisher
In one paragraph

Article in Journal of clinical neurology (Seoul, Korea), 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact, top 87% 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

2 citing papers in PubMed, 1 citations in OpenAlex.

  1. Article
  2. 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

13 authors at 3 institutions in 3 countries.

Kiran Polavarapu *Department of Neurology, National Institute of Mental Health and Neurosciences, Bengaluru, India.ORCID https://orcid.org/0000-0002-8879-6001
Mainak Bardhan *Department of Neurology, National Institute of Mental Health and Neurosciences, Bengaluru, India.ORCID https://orcid.org/0000-0002-4106-409X
Ram Murthy AnjanappaDepartment of Human Genetics, National Institute of Mental Health and Neurosciences, Bengaluru, India.ORCID https://orcid.org/0000-0002-1127-8871
Seena VengalilDepartment of Neurology, National Institute of Mental Health and Neurosciences, Bengaluru, India.ORCID https://orcid.org/0000-0002-0629-9221
Veeramani Preethish-KumarDepartment of Neurology, National Institute of Mental Health and Neurosciences, Bengaluru, India.ORCID https://orcid.org/0000-0003-1158-0971
Leena ShingaviDepartment of Neurology, National Institute of Mental Health and Neurosciences, Bengaluru, India.ORCID https://orcid.org/0000-0002-8596-1120
Tanushree ChawlaDepartment of Neurology, National Institute of Mental Health and Neurosciences, Bengaluru, India.
Saraswati NashiDepartment of Neurology, National Institute of Mental Health and Neurosciences, Bengaluru, India.ORCID https://orcid.org/0000-0002-3184-2345
Dhaarini MohanDepartment of Neurology, National Institute of Mental Health and Neurosciences, Bengaluru, India.
Gautham ArunachalDepartment of Human Genetics, National Institute of Mental Health and Neurosciences, Bengaluru, India.
Thenral S GeethaMedgenome, Medgenome Labs, Bommasandra, Bangalore, India.
Vedam RamprasadMedgenome, Medgenome Labs, Bommasandra, Bangalore, India.
Atchayaram NaliniDepartment of Neurology, National Institute of Mental Health and Neurosciences, Bengaluru, India. atchayaramnalini@yahoo.co.in.ORCID https://orcid.org/0000-0001-9791-3639
National Institute of Mental Health and Neurosciences · INSciGenom Labs (India) · INUniversity of Ottawa · CA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

background and purposePathogenic variants in the myopalladin gene (

methodsA detailed evaluation was conducted of the clinical, muscle magnetic resonance imaging (MRI), and genetic findings of two unrelated adults with

resultsTwo unrelated adults born to consanguineous parents, a 28-year-old male and a 23-year-old female, were diagnosed with pathogenic variants in

conclusionsThis study elaborates on two patients with homozygous

Indexed as

cap myopathymusclemyopalladinMYPNnemaline rod myopathy

Identifiers

PMID34184449
PMCPMC8242322
OpenAlexW3174645094

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.