Evidence map›Paper›PMID 38229655›Full record

ArticleAnnals of Indian Academy of Neurology

Clinical and Genetic Analysis of A Father-Son Duo with Monomelic Amyotrophy: Case Report.

Shiffali Khurana, Abhishek Vats, Mandaville Gourie-Devi, Ankkita Sharma, Sagar Verma, Mohammed Faruq, Uma Dhawan, Vibha Taneja

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

Article in Annals of Indian Academy of Neurology. 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
0.4field-weighted citation impact, top 35% 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

1 citing paper in PubMed, 2 citations in OpenAlex.

  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

8 authors at 3 institutions in 1 country.

Shiffali KhuranaDepartment of Biotechnology and Research, Sir Ganga Ram Hospital, Delhi, India.
Abhishek VatsDepartment of Biotechnology and Research, Sir Ganga Ram Hospital, Delhi, India.
Mandaville Gourie-DeviDepartment of Neurophysiology, Sir Ganga Ram Hospital, Delhi, India.
Ankkita SharmaDepartment of Neurophysiology, Sir Ganga Ram Hospital, Delhi, India.
Sagar VermaDepartment of Biotechnology and Research, Sir Ganga Ram Hospital, Delhi, India.
Mohammed FaruqCouncil of Scientific and Industrial Research, Institute of Genomics and Integrative Biology, Delhi, India.
Uma DhawanDepartment of Biomedical Science, Bhaskaracharya College of Applied Sciences, University of Delhi, Delhi, India.
Vibha TanejaDepartment of Biotechnology and Research, Sir Ganga Ram Hospital, Delhi, India.
Sir Ganga Ram Hospital · INUniversity of Delhi · INCouncil of Scientific and Industrial Research · IN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Monomelic Amyotrophy (MMA) is a rare neurological disorder restricted to one upper limb, predominantly affecting young males with an unknown aetiopathogenesis. We report a familial case of father-son duo affected by MMA. Whole exome sequencing identified genetic variations in

Indexed as

ARPP21familial monomelic amyotrophyRYR3SLIT1whole exome sequencing

Identifiers

PMID38229655
PMCPMC10789418
OpenAlexW4387096576

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.