Evidence map›Paper›PMID 39397192›Full record

ArticleFrontiers of medicine2024

First insights into genotype and phenotype of familial amyotrophic lateral sclerosis in Egypt: early onset and high consanguinity.

Nabila Hamdi, Kathrin Mueller, Amr Hamza, Radwa Soliman, Enass Onbool, Kareem Omran, Omnia Ocab, Axel Freischmidt, Reiner Siebert, Albert Ludolph and 1 more

Abstract readLetter
PubMed Publisher
In one paragraph

Article in Frontiers of medicine, 2024. 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
–field-weighted citation impact
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.

  1. Article
  2. Review
  3. Review
  4. Tofersen and other antisense oligonucleotides in ALS.Therapeutic advances in neurological disorders · 2025
    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

11 authors.

Nabila HamdiMolecular Pathology Unit, The German University in Cairo, New Cairo City, 11835, Egypt. nabila.hamdi@guc.edu.eg.
Kathrin MuellerInstitute of Human Genetics, Ulm University and Ulm University Medical Center, Ulm, 89081, Germany.
Amr HamzaMolecular Pathology Unit, The German University in Cairo, New Cairo City, 11835, Egypt.
Radwa SolimanNeuromuscular Unit, Faculty of Medicine, Ain Shams University, Cairo, 11591, Egypt.
Enass OnboolNeuromuscular Unit, Faculty of Medicine, Ain Shams University, Cairo, 11591, Egypt.
Kareem OmranNeuromuscular Unit, Faculty of Medicine, Ain Shams University, Cairo, 11591, Egypt.
Omnia OcabMolecular Pathology Unit, The German University in Cairo, New Cairo City, 11835, Egypt.
Axel FreischmidtDepartment of Neurology, Ulm University, Ulm, 89081, Germany.
Reiner SiebertInstitute of Human Genetics, Ulm University and Ulm University Medical Center, Ulm, 89081, Germany.
Albert LudolphDepartment of Neurology, Ulm University, Ulm, 89081, Germany.
Nagia FahmyNeuromuscular Unit, Faculty of Medicine, Ain Shams University, Cairo, 11591, Egypt.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Identifiers

PMID39397192

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.