Evidence map›Paper›PMID 33193012›Full record

ArticleFrontiers in neurology2020

Novel Homozygous Missense Mutation in the

Liena E O Elsayed, Inaam N Mohammed, Ahlam A A Hamed, Maha A Elseed, Mustafa A M Salih, Ashraf Yahia, Rayan Abubaker, Mahmoud Koko, Amal S I Abd Allah, Mustafa I Elbashir and 4 more

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

Article in Frontiers in neurology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.7field-weighted citation impact, top 32% 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

4 citing papers in PubMed, 8 citations in OpenAlex.

  1. Arginase 1 deficiency: a treatable form of spastic paraplegia.Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology · 2025
    Review
  2. Article
  3. Article
  4. Pathogenic Variants inFrontiers in neurology · 2021
    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

14 authors at 6 institutions in 4 countries.

Liena E O ElsayedFaculty of Medicine, University of Khartoum, Khartoum, Sudan.
Inaam N MohammedFaculty of Medicine, University of Khartoum, Khartoum, Sudan.
Ahlam A A HamedFaculty of Medicine, University of Khartoum, Khartoum, Sudan.
Maha A ElseedFaculty of Medicine, University of Khartoum, Khartoum, Sudan.
Mustafa A M SalihDivision of Pediatric Neurology, Department of Pediatrics, College of Medicine, King Saud University, Riyadh, Saudi Arabia.
Ashraf YahiaFaculty of Medicine, University of Khartoum, Khartoum, Sudan.
Rayan AbubakerDepartment of Molecular Biology, Institute of Endemic Diseases, University of Khartoum, Khartoum, Sudan.
Mahmoud KokoDepartment of Neurology and Epileptology, Hertie Institute for Clinical Brain Research, Tuebingen, Germany.
Amal S I Abd AllahFaculty of Medicine, University of Khartoum, Khartoum, Sudan.
Mustafa I ElbashirFaculty of Medicine, University of Khartoum, Khartoum, Sudan.
Muntaser E IbrahimDepartment of Molecular Biology, Institute of Endemic Diseases, University of Khartoum, Khartoum, Sudan.
Alexis BriceInstitut du Cerveau, INSERM, CNRS, Sorbonne Université, Paris, France.
Ammar E AhmedFaculty of Medicine, University of Khartoum, Khartoum, Sudan.
Giovanni StevaninInstitut du Cerveau, INSERM, CNRS, Sorbonne Université, Paris, France.
University of Khartoum · SDÉcole Pratique des Hautes Études · FRHertie Institute for Clinical Brain Research · DEKing Saud University · SAPitié-Salpêtrière Hospital · FRSorbonne Université · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

ARG1 genehyperargininemiaspastic quadriplegiaSudanwhole exome sequencing

Identifiers

PMID33193012
PMCPMC7658625
OpenAlexW3097448175

What OpenQuestion holds

Textmetadata
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.